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12,910 open roles across pharma, biotech, medical devices, and clinical research.

NiCE logo

AI Product Manager

NiCE

Southampton, England, UK

At NiCE, we don’t limit our challenges. We challenge our limits. Always. We’re ambitious. We’re game changers. And we play to win. We set the highest standards and execute beyond them. And if you’re like us, we can offer you the ultimate career opportunity that will light a fire within you. **So, what’s the role all about?** We are seeking a mission\-driven AI Product Manager to help build ethical, high\-impact AI solutions for the **Public Safety and Justice** sector. In this role, you will bridge the gap between complex machine learning capabilities and the real\-world needs of first responders, 911 center personnel, legal professionals, and community stakeholders. You will help define products that improve emergency response times, streamline judicial workflows, and ensure AI is deployed responsibly in the public interest. **Key Responsibilities** * Discovery \& Research: Conduct interviews with law enforcement, emergency dispatchers, or legal clerks to identify pain points that can be solved via AI (e.g., automated transcription, predictive resource allocation, or evidence management). * Feature Definition: Translate user needs into clear PRDs (Product Requirement Documents), user stories, and technical specifications for engineering and data science teams. - Strategic Market Intelligence: * Conduct regular competitive analysis of key players in the Public Safety and Security market(e.g., Motorola Solutions, Axon, Mark43\) to identify feature gaps and market opportunities. * Perform "gap analysis" on competitor documentation and public APIs to inform our technical roadmap. - AI Trend Monitoring: * Stay at the forefront of AI breakthroughs, specifically monitoring advancements in Generative AI for casework, computer vision for weapon detection, and Drone as First Responder (DFR) * Evaluate how new models (e.g., from OpenAI or Anthropic) can be integrated into public safety \& Justice workflows responsibly. * Roadmap Support: Help prioritize the product backlog based on impact, technical feasibility, and the unique regulatory constraints of the justice system. **Required Qualifications** * Education: Bachelor’s degree in Computer Science, Data Science, or a related field. * Experience: + 3\-5 years of experience in delivering SaaS related offerings to market + 1\-3 years of experience in working with Generative AI technologies * Technical Literacy: A foundational understanding of the ML lifecycle (data labeling, training, testing, and deployment). * Analytical Mindset: Ability to use data to justify product decisions and measure success through KPIs like model accuracy vs. human\-in\-the\-loop efficiency. * Communication: Exceptional ability to synthesize complex technical trends into actionable business insights. **Preferred Skills** * Understanding of the Public Safety and Justice markets(CAD/RMS systems, Case Management Systems, Body\-Worn Cameras, Digital Evidence Management). * Experience with LLMs (Large Language Models) or Computer Vision. * Knowledge of data privacy laws and ethical AI frameworks. **Why Join Us?** You will be at the forefront of a technological revolution in the public sector, creating tools that don't just drive profit, but actively save lives and ensure a fairer justice system. **What’s in it for you?** Join an ever\-growing, market\-disrupting, global company where the teams – comprised of the best of the best – work in a fast\-paced, collaborative, and creative environment! As the market leader, every day at NICE is a chance to learn and grow, and there are endless internal career opportunities across multiple roles, disciplines, domains, and locations. If you are passionate, innovative, and excited to constantly raise the bar, you may just be our next NICEr! **Enjoy NICE\-FLEX!** At NICE, we work according to the NICE\-FLEX hybrid model, which enables maximum flexibility: 2 days working from the office and 3 days of remote work, each week. Naturally, office days focus on face\-to\-face meetings, where teamwork and collaborative thinking generate innovation, new ideas, and a vibrant, interactive atmosphere. **Requisition ID: 11275** **Reporting to: Director, Product Management** **Role Type: Individual Contributor** **About NiCE** *NICE Ltd. (NASDAQ: NICE) software products are used by 25,000\+ global businesses, including 85 of the Fortune 100 corporations, to deliver extraordinary customer experiences, fight financial crime and ensure public safety. Every day, NiCE software manages more than 120 million customer interactions and monitors 3\+ billion financial transactions.* *Known as an innovation powerhouse that excels in AI, cloud and digital, NiCE is consistently recognized as the market leader in its domains, with over 8,500 employees across 30\+ countries.* *NiCE is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, age, sex, marital status, ancestry, neurotype, physical or mental disability, veteran status, gender identity, sexual orientation or any other category protected by law.*

Healthtech & Digital Health
Nuvei logo

VP, Head of Product Marketing

Nuvei

London, England, UK

The world of payment processing is rapidly evolving, and businesses are looking for loyal and strategic partners, to help them grow. Meet Nuvei, Nuvei is the global fintech building the infrastructure for every payment, everywhere. Its modular, flexible, and scalable technology enables leading companies to accept next\-generation payments, offer all payout options, and benefit from card issuing, banking, risk, and fraud management services. Connecting businesses to their customers in more than 200 markets, with local acquiring in 52 markets, 150 currencies, and over 720 alternative payment methods, Nuvei provides the technology and insights for customers and partners to succeed locally and globally through one integration. At Nuvei, we live our core values, and we thrive on solving complex problems. We're dedicated to continually improving our product and providing relentless customer service. We are always looking for exceptional talent to join us on the journey! **Position Summary** The VP Head of Product Marketing is responsible for defining how Nuvei's products are positioned, packaged, launched, enabled, adopted and scaled across global markets. Reporting to the CMO, this role sits at the intersection of Product, Commercial, Marketing and Customer Success, translating product capabilities into compelling market narratives, differentiated positioning, repeatable go\-to\-market motions and measurable commercial outcomes. The role owns the full product marketing lifecycle—from market intelligence and customer insights through positioning, launch planning, sales enablement and post\-launch adoption—ensuring Nuvei's products are not only built successfully but understood, adopted and sold successfully. * This role is open to all locations in Europe, you should just be able to work in your chosen country without requiring sponsorship\* **Key Responsibilities** **Product Positioning \& Messaging:** * Own the positioning, messaging and narrative architecture for Nuvei's product portfolio * Develop product value propositions for different industries, buyer personas and geographies * Maintain competitive differentiation and category positioning * Translate technical product capabilities into compelling commercial stories * Ensure consistency of product narratives across sales, marketing, analyst and partner communications * Design product naming strategy and architecture **Go\-To\-Market Strategy** * Lead global go\-to\-market planning and execution for major launches, partnerships and strategic initiatives * Define launch strategies, market prioritization and rollout approaches * Establish launch tiering and prioritization frameworks * Partner with regional teams on localization and market\-specific execution * Drive adoption beyond product launch through structured growth and reinforcement programs **Sales Enablement** * Own global product sales enablement * Develop training programs, playbooks, battlecards, talk tracks, FAQs and commercial collateral * Define "ready\-to\-sell" requirements and commercialization gates * Deliver live and on\-demand training to commercial teams * Drive continued product adoption through just\-in\-time enablement models and AI\-supported learning experiences **Training The Sales Organization** * Design and deliver structured product training programs that equip Relationship Managers, Sales Development, Account Management and other Commercial teams to confidently position, explain and sell Nuvei's products * Build scalable training journeys for new product launches, onboarding, refresher learning and advanced product education * Ensure sales teams can translate product capabilities into relevant customer conversations, objection handling, competitive differentiation and commercial value * Measure training effectiveness through readiness, adoption, usage, pipeline influence and feedback from Commercial teams **Shaping The Product Roadmap** * Systematically capture, synthesize and prioritize input from Commercial teams to inform product roadmap decisions * Translate frontline feedback, customer demand signals, deal blockers, competitive insights and regional market needs into clear product recommendations * Partner with Product leadership to ensure roadmap priorities are grounded in commercial reality and aligned with Nuvei's growth priorities * Create structured feedback loops between Product, Commercial and Customer\-facing teams to improve product\-market fit and accelerate adoption **Market Intelligence \& Customer Insights** * Lead competitive intelligence and market analysis programs * Conduct win/loss reviews and customer research * Define ideal customer profiles and segmentation strategies * Gather feedback from customers, sales teams, partners and analysts to shape positioning and roadmap recommendations * Monitor industry, regulatory and competitor developments **Analyst \& Influencer Relations** * Manage product\-facing analyst engagement activities * Lead participation in analyst evaluations and market assessments * Develop thought leadership initiatives aligned to product strategy * Build relationships with analysts, partners and industry influencers **Team Leadership** * Lead, coach and develop the Product Marketing team * Build expertise across positioning, commercialization, competitive intelligence and enablement * Establish scalable operating models, processes and best practices * Drive collaboration across Product, Marketing, Commercial and Customer\-facing teams **Requirements** * 10\+ years of experience in Product Marketing, Go\-To\-Market, Commercial Strategy or related roles * Experience in payments, fintech, SaaS, commerce or technology businesses * Proven success launching and scaling complex products globally * Strong positioning, messaging and storytelling capabilities * Experience working closely with Product Management and Commercial teams * Strong project leadership and stakeholder management skills * Experience building sales enablement and commercialization programs **Benefits** **The annual salary range for this role in these primary locations are:** **Netherlands: €138,000\-€158,000** **Spain: €135,000\-€151,000** **France: €135,000\-€154,000** **Germany: €135,000\-€156,000** **Italy: €130,000\-€150,000** **Portugal: €130,000\-€149,000** * These are all Gross (before tax)\* This range represents the expected starting salary for candidates hired into this role in the specified location. If the position is filled in a different location, a different salary range may apply due to objective factors such as local labor market conditions and cost of living. This salary range may be inclusive of several career levels at Nuvei and will be narrowed during the interview process based on a number of factors, including the candidate's experience, qualifications, and specific location. Applicants not located in the primary location may request the annual salary range for their location during the interview process. Specific benefits and details about what compensation is included in the salary range listed above will vary depending on the applicant's location and can be discussed in more detail during the interview process. Nuvei is an equal\-opportunity employer that celebrates collaboration and innovation and is committed to developing a diverse and inclusive workplace. The team at Nuvei is comprised of a wealth of talent, skill, and ambition. We believe that employees are happiest when they're empowered to be their true, authentic selves. ***So, please come as you are. We can't wait to meet you*** **Our recruitment process may use automated tools, including AI, to support application management and candidate shortlisting.**

Healthtech & Digital Health
Medpace logo

eClinical Coordinator (London)

Medpace

London, England, UK

Our corporate activities are growing rapidly, and we are currently seeking a full\-time, office\-based eClinical Coordinator to join our Data Management team in Central London. The eClinical Coordinator at Medpace is a **crucial component of the clinical trial process.** By working with the eClinical Project Manager and other team members, these professionals ensure the accuracy of data reported by patients for clinical studies. At Medpace, eClinical Coordinators go through an **extensive onboarding and training process** , which prepares them to become experts in their field. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. **Responsibilities** * Participate as part of a team on various project(s). * Work with vendors to ensure patient forms meet their respective electronic requirements. * Partner with Sponsors to develop application requirements for each unique study. * Assist in the creation and maintenance of metric reports and study specific documents. * Assist Clinical Db Programmers with configuring and testing applications. * Troubleshoot issues with applications by working with sites/sponsors. * Report compliance metrics to Sponsors. **Qualifications** * Bachelor's degree in Life Sciences or Mathematics * Strong attention to detail * Excellent working knowledge of Microsoft Excel and Word * Solid oral and written English Language communication skills * 1\-2 years of experience in a pharmaceutical or CRO setting preferred. **Medpace Overview** Medpace is a full\-service clinical contract research organization (CRO) providing phase l\-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in\-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40\+ countries. **Why Medpace?** When you join Medpace, you become part of an innovative team that brings cutting\-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross\-functional collaboration. ***Purpose\-Driven Work*** * + Work alongside physicians, scientists, and industry\-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence ***Collaborative Culture*** * + Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. + Leadership throughout Medpace is both accessible and approachable ***Continuous Growth \& Development*** * + Office based environment with on\-site mentors + Defined career paths with clear advancement opportunities + Industry renowned onboarding and training programs designed to accelerate professional development + Ongoing training and continuous learning opportunities throughout your career + An environment that encourages employees to influence change, contribute ideas, and grow quickly **Other Employee Benefits** * + Competitive compensation programs that recognize and reward performance + Comprehensive health, wellness, retirement, and PTO benefits + Office based culture with occasional WFH that provides flexibility for eligible positions after training + Company\-sponsored social events *Please note benefits may vary based on country.* **What To Expect Next** A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Research
Medpace logo

Associate Clinical Trial Manager (PhD) - Cardiovascular

Medpace

Stirling, Scotland, UK

Medpace is currently seeking candidates with **Cardiovascular related PhDs and/or Post\-Doctoral Research experience** for a full\-time, office\-based Associate Clinical Trial Manager (aCTM) to join our Scotland, **Stirling** Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and **develop their career in the research and development of cutting\-edge therapeutics** . Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). **Responsibilities** * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager * Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy * Compile and maintain project\-specific status reports within the clinical trial management system * Interact with the internal project team, Sponsor, study sites, and third\-party vendors * Provide oversight and quality control of our internal regulatory filing system * Provide oversight and management of study supplies * Create and maintain project timelines * Coordinate project meetings and produce quality minutes **Qualifications** * PhD in Life Sciences * Fluency in English with solid presentation skills * Ability to work in a fast\-paced dynamic industry within an international team * Prior experience within the CRO or pharmaceutical industry not required but will be advantageous **Medpace Overview** Medpace is a full\-service clinical contract research organization (CRO) providing phase l\-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in\-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40\+ countries. **Why Medpace?** When you join Medpace, you become part of an innovative team that brings cutting\-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross\-functional collaboration. ***Purpose\-Driven Work*** * + Work alongside physicians, scientists, and industry\-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence ***Collaborative Culture*** * + Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. + Leadership throughout Medpace is both accessible and approachable ***Continuous Growth \& Development*** * + Office based environment with on\-site mentors + Defined career paths with clear advancement opportunities + Industry renowned onboarding and training programs designed to accelerate professional development + Ongoing training and continuous learning opportunities throughout your career + An environment that encourages employees to influence change, contribute ideas, and grow quickly **Other Employee Benefits** * + Competitive compensation programs that recognize and reward performance + Comprehensive health, wellness, retirement, and PTO benefits + Office based culture with occasional WFH that provides flexibility for eligible positions after training + Company\-sponsored social events *Please note benefits may vary based on country.* **What To Expect Next** A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Pharma & Biotech
Prolific logo

Senior Product Manager - AI

Prolific

London, England, UK

***Senior Product Manager, Prolific for AI*** *Team: Product, Research \& Design* *Prolific* Prolific is not just another player in the AI space – we are the architects of the human data infrastructure that's reshaping the landscape of AI development. In a world where foundational AI technologies are increasingly commoditized, it's the quality and diversity of human\-generated data that truly differentiates products and models. *The Role* As we scale our AI Product Group, we're looking for a Senior Product Manager to take founder\-level ownership of the tooling that lets frontier AI model developers conduct cutting\-edge research on Prolific. Increasingly, our AI customers are among the leading AI companies in the world, and this role will additionally lead a team of client\-facing engineers dedicated to building strategic integrations and rapid, bespoke development for their most demanding needs. You'll report into the AI Lead, and join a brilliant team of Product Managers building next\-generation AI tooling within our AI Product Group. **Impact:** You'll be the Product person accountable for the outcomes of a stream\-aligned team building next\-gen tooling for frontier AI model developers, and also prioritise for impact the work of a client\-facing engineering team. This is a career\-defining moment to shape how some of the world's biggest technology companies build AI – no big deal. You'll own how our most strategic AI clients experience Prolific end to end, from product to bespoke integration. **Experience:** You'll bring experience building AI native systems, with particular experience building AI native UX. You'll have had success taking complex human workflows and distilling them into highly adaptable technical systems, then scaling access to those systems across multiple interaction surfaces – UI, APIs, CLIs, and MCPs. You'll also have experience directly managing engineers, ideally in a client\-facing or solutions\-engineering capacity, and know how to turn a sophisticated client's bespoke needs into a scalable integration rather than a one\-off fix. **Domain:** You will manage two teams which together give you unmatched closeness and opportunity to build tools for the companies and researchers driving the AI frontier. The Data Collection Tooling team is responsible for building and scaling the systems that enable high\-quality human data collection for AI training and evaluation. Additionally the strategic integrations team interfaces directly with our biggest AI accounts for custom builds. It's critical that the person in this role prioritizes both intuitively and systematically, and is a master at the elegant art of trade\-offs between the here and now and the future. **Responsibilities:** You'll product manage a stream\-aligned team of your own, and lead a team of client\-facing engineers delivering strategic integrations and rapid, custom development for our most strategic AI accounts. You'll be accountable for the outcomes of both, and be the key driver of interaction with your peer teams, collaborating across domains of science, research, supply, sales, and account services. **Culture:** Adding on to our Prolific Principles, we expect colleagues in the Product, Research, and Design Group to demonstrate reliability, grit, diplomacy, a bias for action, and a dogged focus on value – you'll be a champion of these behaviours yourself, and in the culture of your team. Accountability and autonomy are two sides of the same coin, and we expect you to demonstrate both. *What you'll be doing* * Build and launch the next generation of Prolific's Data Collection Tooling product suite. * Lead a team of client\-facing engineers delivering strategic integrations and rapid, custom development for our most demanding AI accounts. * Stay up to speed with the rapidly changing face of frontier AI research, keeping your product ahead of customer needs. * Run the end\-to\-end product development lifecycle, from strategy to success metrics to roadmap, delivery, and iteration – communicating that strategy clearly to executives while working through the details with your team. * Be an unblocker and simplifier of complexity: colleagues will bring you problems, and emerge optimistic, with solutions. * Partner productively with Product Design, User Research, Analytics, and Engineering in a test\-learn\-iterate fashion. *What you'll bring* * An extensive and varied track record building AI\-native products and UX, including scaling access across multiple interaction surfaces such as UI, APIs, CLIs, and MCPs. * Experience directly managing engineers, ideally in a client\-facing or solutions\-engineering capacity, and turning sophisticated clients' bespoke needs into scalable integrations. * Fluency in modern Product/Engineering practice: Agile, continuous discovery and delivery, JTBD, vertical slicing, test\-learn\-iterate. * Strong commercial acumen and data\-informed decision\-making, paired with a storyteller's flair and a relentless can\-do attitude. *Even better if you have* * Experience building for or with frontier AI labs or major technology companies. * A track record of giving back to your Product community. *Why Prolific is a great place to work* We've built a unique platform that connects researchers and companies with a global pool of participants, enabling the collection of high\-quality, ethically sourced human behavioral data and feedback. This data is the cornerstone of developing more accurate, nuanced, and aligned AI systems. We believe that the next leap in AI capabilities won't come solely from scaling existing models, but from integrating diverse human perspectives and behaviors into AI development. By providing this crucial human data infrastructure, Prolific is positioning itself at the forefront of the next wave of AI innovation – one that reflects the breath and the best of humanity. Working for us will place you at the forefront of AI innovation, providing access to our unique human data platform and opportunities for groundbreaking research. Join us to enjoy a competitive salary, benefits, and remote working within our impactful, mission\-driven culture. *Links to more information on Prolific* **Benefits** External Handbook Website Youtube *Privacy Statement* **By submitting your application, you agree that Prolific may collect your personal data for recruiting and global organisation planning. Prolific's Candidate Privacy Notice explains what personal information Prolific may process, where Prolific may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Prolific use of your personal information.**

Healthtech & Digital Health
Belkin logo

Regional Category Manager (EMEA) – Connectivity & B2B

Belkin

Hemel Hempstead, England, UK

**Job Description** **Who are we?** Today is where the future becomes reality, and that’s why we believe that every “today” should be extraordinary. People\-centric design and an obsession with details are at the core of what we do at Belkin. We empower people to get more life out of every single day with our extensive range of products delivering power, protection, connectivity, audio, and smart home solutions. From humble beginnings in a 1980s Southern California garage to celebrating over 40 years as a market leader and innovator, our ethos has always been about connection. As a diverse, global technology company, Belkin is still inspired and driven by the connection between people and technology. Website: **www.belkin.com** **What You’ll Do** As Regional Category Manager for EMEA within Belkin’s Connectivity business unit, you’ll own the commercial performance of your portfolio and be the go\-to partner for internal teams, customers, and partners across the region. You’ll shape category strategy, guide the end\-to\-end product lifecycle, and work closely with Sales, Global Product, Marketing, and Planning to bring compelling, consumer\-first propositions to market. With ambitious growth plans for Connectivity and B2B, you’ll also play a key role in translating new technology and investment into winning roadmaps, launches, and in\-market execution across EMEA. **How You’ll Do It** * Own commercial performance (P\&L): Lead pricing, promotions, and profitability strategies, partnering with regional Sales teams to build pipeline and deliver revenue. * Lead the full product lifecycle: Identify market opportunities, drive NPI (New Product Introduction) for connectivity, and manage through to end\-of\-life planning. Continuously optimise the portfolio based on performance, trends, and strategic priorities. * Set strategy and build roadmaps: Define category, channel, and go\-to\-market strategy for Connectivity in EMEA, maintaining a product roadmap aligned to consumer needs, market trends, competitive dynamics, and business objectives. * Turn insights into action: Gather and analyse market data, competitive intelligence, and customer feedback across the category—then translate insights into clear recommendations for Sales, the Business Unit, and senior stakeholders. * Deliver great launches: Lead product launches across EMEA in partnership with Channel Marketing and cross functional team. Deliver sales tools, training, and product collateral that clearly communicate technical benefits, fit, and consumer value. * Be the EMEA voice to Global Product: Act as the key liaison between EMEA and Global Product Management, sharing performance updates, customer feedback, and market learnings in monthly/quarterly reviews—and shaping priorities for new technology and investment in Connectivity. * Work cross\-functionally to execute: Partner with Planning, Sales, and Marketing to support availability, healthy inventory levels, and strong local execution across EMEA markets. * Improve how we work: Support the Senior Category Manager/Director of Category Management to embed best practices and continuous improvements that increase efficiency and commercial impact. **What You’ll Need** * Experience in Product Management or Category Management in a comparable commercial role (Consumer Electronics, IT, or retail buying experience is a strong plus.) * Strong commercial acumen and a track record of delivering category growth. * Confidence leading cross\-functional initiatives and influencing stakeholders across countries and functions. * Comfortable presenting to retail customers and internal senior leadership. * A proactive, results\-driven approach and the ability to manage multiple priorities at pace. * Strong analytical and problem\-solving skills, with a structured approach to turning data into decisions. * Clear, confident communication skills—able to simplify complex topics for different audiences. * Strong capability with Excel, PowerPoint, and standard business tools, including commonly used generative AI tools * Bachelor’s degree in Business, Marketing, or a related field (or equivalent practical experience). **What You’ll Get In Return** * Permanent Full Time (40 hours a week), Monday \- Friday * Competitive Salary, Benefits and Bonus Plan * Flexible hybrid working (3 days office, 2 days remote) * Optional Private Health Insurance \& Dental Insurance * Pension * Life Assurance \& Income Protection Insurance * Employee Assistance Programme * 25 days holiday (increasing to 30 days after 5 years) \& Bank Holidays * Birthday Day off * Belkin Product Employee Discount Programme Location: Kings Langley, UK **What You’re Getting Into** We’ve got big collaborative spaces for your big ideas, so bring an open mind and leave your suit in the closet. We all are committed to creating unique and rewarding consumer experiences. Everyone is interested in succeeding – for the team, for themselves and for the business. Cross\-functionally and across the company, everyone has common goals and aspires to be their best. You will learn something new or at least look at things differently every day. There are so many smart and creative people around that you’ll be motivated to pursue the ideal. Team spirit is infectious. Belkin is an extremely open workplace, where communication is essential. Not every idea will be accepted, but you’ll be asked for your point of view. Innovation thrives on multiple and varied levels. At Belkin we challenge conventional wisdom and refuse to accept that something cannot be done. Belkin is an Equal Opportunity and Affirmative Action Employer Disability and Veterans. We maintain a drug\-free workplace. All candidates applying for a job in the EMEA region, please review the Applicant Privacy notice HERE Location: Kings Langley,

Medical Device
Google logo

Product Manager, Health and Home Infrastructure

Google

London, England, UK

**Minimum qualifications:** * Bachelor's degree or equivalent practical experience. * 5 years of experience in product management or a related technical role. * 2 years of experience taking technical products from conception to launch (e.g., ideation to execution, end\-to\-end, 0 to 1, etc.). * Experience integrating generative Artificial Intelligence (AI) tools or Large Language Model (LLM) interfaces into workflows. **Preferred qualifications:** * Experience in data infrastructure and analytics, software experimentation systems, or both. * Familiarity with AI/ML infrastructure. * Excellent communication skills (e.g,, written, verbal). * Strong cross\-functional and cross\-organizational collaboration skills, especially with engineering and data science. * Adept at using AI tools to amplify Product Manager (PM) impact. **About The Job** At Google, we put our users first. The world is always changing, so we need Product Managers who are continuously adapting and excited to work on products that affect millions of people every day. In this role, you will work cross\-functionally to guide products from conception to launch by connecting the technical and business worlds. You can break down complex problems into steps that drive product development. One of the many reasons Google consistently brings innovative, world\-changing products to market is because of the collaborative work we do in Product Management. Our team works closely with creative engineers, designers, marketers, etc. to help design and develop technologies that improve access to the world's information. We're responsible for guiding products throughout the execution cycle, focusing specifically on analyzing, positioning, packaging, promoting, and tailoring our solutions to our users. **Responsibilities** * Own and drive roadmap and delivery for offline data infrastructure supporting Home and Health. Improve data access for subs/growth, agentic access, etc. including logging, observability, debuggability requirements. * Own and drive roadmap and delivery for experiments infrastructure supporting Home and Health. Improve the velocity of experiment design, configuration, analysis, and decision\-making. * Communicate product roadmaps to user community; define and drive user engagement strategies to validate the roadmap and deliver value. Empower teams to run more complex/nuanced experiments (multi\-arm) to support product innovation and decision\-making. * Set key product metrics and Key Performance Indicators (KPIs) for offline data and experiments infrastructure. * Define and ship analytics back\-ends that process data and turn it into useful insights. Consolidate logging systems that works across multiple product lines and identify requirements and use cases, system characteristics, and set target metrics. Google is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. See also Google's EEO Policy and EEO is the Law. If you have a disability or special need that requires accommodation, please let us know by completing our Accommodations for Applicants form .

Healthtech & Digital Health
Intuitive logo

Endoluminal Sales Manager - UK

Intuitive

Manchester, England, UK

**Company Description** It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at **Intuitive** . As a global leader in **robotic\-assisted surgery** and **minimally invasive care** , our technologies—like the **da Vinci surgical system** and **Ion** —have transformed how care is delivered for millions of patients worldwide. We’re a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world. The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful—because every improvement we make has the potential to change a life. If you’re ready to contribute to something bigger than yourself and help **transform the future of healthcare** , you’ll find your purpose here. **Job Description** At Intuitive, we are united behind our mission: we believe that minimally invasive care is life\-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As pioneer and leading company in the field of robotic\-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare’s hardest challenges and advance what is possible. Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere—we strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves. Passionate people who want to make a difference drive our culture—our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real\-world experiences to help us think in new ways. We actively invest in our team members to support their long\-term growth so they can continue to advance our mission and achieve their highest potential. Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let’s advance the world of minimally invasive care. **Primary Function Of Position** An Endoluminal Sales Manager is responsible for selling the Ion Endoluminal System to greenfield and existing hospitals within the assigned territory. The role requires expert knowledge of diagnostic robotics, consultative and executive selling, the ability to build multidisciplinary advocacy teams, and the leadership to manage complex capital sales from opportunity identification through implementation. The Endoluminal Sales Manager serves as the strategic commercial lead for each opportunity, partnering cross\-functionally to accelerate market adoption and deliver sustainable procedural growth. **Roles And Responsibilities** * Manage the complete capital sales process from prospecting to contract signature and installation * Develop territory and strategic account plans aligned with regional business objectives. * Build executive, clinical and economic advocacy across C\-suite, physicians, procurement and hospital administration. * Lead executive presentations, business case discussions and value\-based selling initiatives. * Drive market development by identifying new accounts, clinical champions and key opinion leaders. * Coordinate complex cross\-functional deal teams including Clinical Sales, Marketing, Market Access, Finance, Legal, Service and Operations * Support tenders, procurement processes and contract negotiations. Ensure smooth transition from capital sale to clinical implementation and procedural adoption. * Maintain accurate CRM pipeline, forecasting and opportunity management. * Travel extensively (approximately 70%) **Qualifications** **Performance Objectives:** * Consistently achieve quarterly and annual sales targets. * Develop sustainable customer relationships across assigned territory. * Create compelling financial and clinical business cases. * Drive forecast accuracy and disciplined pipeline management. * Expand market awareness and accelerate adoption of the Ion platform. * Ensure successful implementation and long\-term customer success. **Qualifications Required** **Required Knowledge, Skills, and Experience:** * Minimum 5 years of medical device sales experience. * Experience selling capital medical equipment preferred. * Strong executive communication and presentation skills. * Knowledge of bronchoscopy, endoscopy and/or operating room environments. * Demonstrated strategic account management and complex stakeholder management. * Ability to work cross\-functionally within a matrix organization. * Strong analytical, negotiation and business planning skills. * Willingness to travel extensively. Additional Information Intuitive is an Equal Employment Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws. We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws. U.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR * 743\.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status. Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government’s licensing process can take 3 to 6\+ months) or (ii) implement a Technology Control Plan (“TCP”) (note: typically adds 2 weeks to the hiring process). For any Intuitive role subject to export controls, final offers are contingent upon obtaining an approved export license and/or an executed TCP prior to the prospective employee’s start date, which may or may not be flexible, and within a timeframe that does not unreasonably impede the hiring need. If applicable, candidates will be notified and instructed on any requirements for these purposes. This position may be filled at a different job level than listed here depending on business need and/or on the selected candidate’s experience, knowledge and skills. Compensation will be based primarily on the job level at which the role is filled and the **Candidate’s Qualifications, Consistent With Applicable Law.** **Shift:** Day

Medical Device
IC Resources logo

Radar Signal Processing Consultant

IC Resources

Cambridge, England, UK

We’re supporting a long\-standing client in the defence and security sector who are hiring a **Radar Signal Processing Consultant** to work on advanced radar and Electronic Warfare programmes based just outside Cambridge. As a **Radar Signal Processing Consultant** , you’ll be involved in modelling, simulation and analysis of complex systems, using tools such as MATLAB, Simulink and Python. The work focuses on developing proof\-of\-concept models, signal processing algorithms and simulation environments for radar and EW applications with real\-world national impact. The role is suited to someone who enjoys getting into the detail of difficult technical problems, building models that stand up to scrutiny, and applying signal processing theory to real radar and EW system challenges. **What We’re Looking For** * Experience in radar or Electronic Warfare modelling and simulation * Strong background in signal processing algorithm development and validation * Experience with MATLAB, Simulink, Python or similar high\-level languages * Understanding of system architecture and complex system interactions * A relevant degree in engineering, physics, maths or a related discipline Additional experience in any of the following areas would be highly desirable: * DSP fundamentals including sampling, FFTs, filtering, correlation and convolution * Simulation test bench development * Hardware\-in\-the\-loop development for radar or EW systems * RF system knowledge, including antennas, front\-end architecture, waveforms or receiver processing * Real\-time DSP or FPGA\-based implementation * Simulation validation through real\-world measurements or field trials Candidates with defence, security, radar or Electronic Warfare experience are preferred, though our client is open to applicants from adjacent technical backgrounds if they bring strong modelling, signal processing and problem\-solving skills. Why consider this? This client is growing quickly and investing in technically demanding defence and national security programmes. You’ll be given meaningful technical responsibility, work alongside a highly capable peer group, and operate in a collaborative R\&D environment with strong scope to develop into adjacent disciplines. Benefits include a profit\-related bonus, 10% employer pension contribution, private medical cover for you and your dependants, free daily lunch and refreshments, enhanced parental leave, EV leasing, relocation support where applicable, and modern facilities just outside Cambridge. Due to the nature of the work, you must be eligible for **UK security clearance** . Please note: sponsorship is not available for this position. If you’d like to discuss this **Radar Signal Processing Consultant** position further, please reach out to Zac Taylor at IC Resources.

Pharma & Biotech
Siemens Healthineers logo

RA/CMC Specialist

Siemens Healthineers

London, England, UK

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. As part of Siemens Healthineers, Radiopharma International is at the forefront of radiopharmaceuticals and molecular imaging. We work with some of the world leading research organizations, pioneering new biomarkers and changing nuclear medicine for physicians and patients. With nearly 60 radiopharmaceutical distribution centres across the world, we are one of the largest PET biomarker producers globally. We are committed to developing innovative PET tracer technologies, thus helping to expand and advance the science of molecular imaging. **Your role:** * Ensure product compliance with UK, EU, and international regulations. * Stay updated on relevant legislation and guidelines. * Support EU regulatory team in response to health authority queries (e.g., MHRA). * Prepare CMC variations under tight deadlines and manage regulatory CMC submissions, focusing on EU/UK life cycle maintenance. * Evaluate scientific data for submissions and ensure compliance with corporate and local regulations. * Review submissions for accuracy and consistency. * Collaborate with EU regulatory team and maintain up\-to\-date system records. * Build strong internal and external relationships and deliver on commitments. * Strong communication and collaboration skills. **Your expertise:** * Degree in Chemistry, Pharmacy, or related life science. * 3–5 years’ experience in regulatory CMC, pharmaceutical, biotech, or related fields. * Strong background in module 3 writing and regulatory CMC strategy development. * Strategic, analytical, and problem\-solving mindset. * Excellent communication, teamwork, and time\-management skills. **Benefits:** * 26 days' holiday with the option to buy an additional 10 * Up to 10% employer pension contribution * Share and bonus scheme * Access to our flexible benefits from private medical insurance to dental cover * Corporate Social Responsibility opportunities including 2 paid volunteering days per year and support from our 24/7 employee assistance programme. **Who we are:** We are a team of more than 71,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision\-making and treatment pathways. **How we work:** When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Check our Careers Site at https://www.siemens\-healthineers.com/en\-uk/careers Siemens Healthineers are proud to be a Disability Confident Committed employer. If you require any adjustments at any stage of the recruitment process, please let us know. We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. Please create a profile within our talent community and subscribe to personalized job alert that will keep you posted about new opportunities. **To all recruitment agencies:** Siemens Healthineers' recruitment is internally managed, with external support permitted only when a qualified supplier has established a formal contract with us. Unsolicited candidate submissions and referrals, absent a current supplier contract, do not establish consent and are ineligible for fees. We delete and destroy unsolicited information, thus, would recommend you refrain from any such practices. Your adherence to our policies is appreciated.

Pharma & Biotech
Bank of America logo

UK&I Investment Banking - Associate

Bank of America

London, England, UK

**Job Description:** **Job Title: UK\&I Investment Banking \- Associate** **Corporate Title: Associate** **Location: London, United Kingdom** **Company Overview** At Bank of America, we are guided by a common purpose to help make financial lives better through the power of every connection. We do this by driving Responsible Growth and delivering for our clients, teammates, communities and shareholders every day. Being a Great Place to Work is core to how we drive Responsible Growth. This includes our commitment to being an inclusive workplace, attracting and developing exceptional talent, supporting our teammates’ physical, emotional, and financial wellness, recognizing and rewarding performance, and how we make an impact in the communities we serve. Bank of America is committed to an in\-office culture with specific requirements for office\-based attendance and which allows for an appropriate level of flexibility for our teammates and businesses based on role\-specific considerations. At Bank of America, you can build a successful career with opportunities to learn, grow, and make an impact. Join us! **Responsibilities** As part of the UK and Ireland Investment Banking team you will help advise listed and private clients on the full range of strategic transactions. Working across all sectors and product types, you will be involved in all aspects of regular client coverage and transaction execution, including as financial adviser and corporate broker to a large number of FTSE100 and FTSE250 clients. * Provide strategic financial advice to corporate clients including listed companies, private equity and founder back businesses * Undertake financial analysis including valuation, modelling, trading analysis and transaction comps * Assume responsibility for monitoring and advising clients in terms of macro events, sector news flow and company events * Support on transactions across the full range of strategic events including buyside and sellside M\&A, de\-mergers, P2Ps and private equity monetisations including IPOs (such support may include maintaining financial models, coordinating other advisers, due diligence and timetables) * Research on companies and industries and support on client initiatives including generating and developing new ideas to present * Formulate and develop client pitch\-books and analysis in addition to supporting other bankers within the team * Build and maintain direct client relationships and also foster cross functional relationships with bankers in, sector, product and regional business units **What We Are Looking For** * Team player who enjoys working with a wide variety of clients and colleagues * Strong mathematical and analytical skills as well as proficient level of MS Excel and PowerPoint * Meticulous attention to detail, diligence and conscientiousness * Excellent interpersonal communication skills – ability to build and maintain client relationships * Capable of working effectively both independently and with multiple teams/individuals * Proactive, self starter with genuine interest in the industry and financial services * Educated to degree level (preferably in a numerical discipline such as economics, finance or engineering) **Bank of America** Good conduct and sound judgment is crucial to our long term success. It’s important that all employees in the organisation understand the expected standards of conduct and how we manage conduct risk. Individual accountability and an ownership mind\-set are the cornerstones of our Code of Conduct and are at the heart of managing risk well. We are an equal opportunities employer and ensure that no applicant is subject to less favourable treatment on the grounds of sex, gender identity or gender reassignment, marital or civil partner status, race, religion or belief, colour, nationality, ethnic or national origins, age, sexual orientation, pregnancy or maternity, socio\-economic background, responsibility for dependants or physical or mental disability. The Bank selects candidates for interview based on their skills, qualifications and experience. We strive to ensure that our recruitment processes are accessible for all candidates and encourage any candidates to tell us about any adjustment requirements. Benefits: UK \- 2026 * At Bank of America, we strive to prioritise employees’ health and wellbeing – it’s what makes us a Great Place to Work. * Private healthcare for you and your family plus an annual health screen to help you manage your physical wellness with the option to purchase a screen for your partner * Competitive pension plan, life assurance and group income protection cover if you become unable to work as a result of a disability or health reasons * We offer 26\-weeks paid maternity leave, 16\-weeks paid paternity leave and inclusive family leave arrangements for working parents and carers including 20 days of back\-up childcare including access to school holiday clubs and 20 days of back\-up adult care per annum * The ability to change your core benefits as well as the option of selecting a variety of flexible benefits to suit your personal circumstances including access to a wellbeing account, travel insurance, critical illness, cycle to work etc. * Use of a flex fund to use towards benefits * Access to an emotional wellbeing helpline, and virtual GP services * Access to the Peppy App which provides 1:1 support, consultations and resources relating to men’s health, women’s health, fertility, menopause and pregnancy \& parenthood * Access to a range of gyms, exercise classes and wellbeing Apps through Wellhub, including Headspace and Calm * Ability to donate to charities of your choice directly through payroll and the bank will match your contribution * Opportunity to give back to your community, develop new skills and work with new groups of people by volunteering in your local area Good conduct and sound judgment is crucial to our long term success. It’s important that all employees in the organisation understand the expected standards of conduct and how we manage conduct risk. Individual accountability and an ownership mind\-set are the cornerstones of our Code of Conduct and are at the heart of managing risk well. “We are an equal opportunities employer and ensure that no applicant is subject to less favourable treatment on the grounds of sex, gender identity or gender reassignment, marital or civil partner status, race, religious or similar philosophical belief, political opinion, colour, nationality, ethnic or national origins, age, sexual orientation, pregnancy or maternity, socio\-economic background, responsibility for dependants or physical or mental disability. The Bank selects candidates for interview based on their skills, qualifications and experience.” We strive to ensure that our recruitment processes are accessible for all candidates and encourage any candidates to tell us about any adjustment requirements.

Finance & Investment
Elysium Healthcare logo

Incident Reporting Administrator

Elysium Healthcare

Borehamwood, England, UK

Are you passionate about patient safety, governance and using data to drive meaningful improvements in healthcare? Join Elysium Healthcare as an Incident Reporting Administrator and play a key role in supporting and improving our incident management and patient safety reporting systems. In this rewarding role, you will be responsible for supporting the development, maintenance and continuous improvement of Elysium's Incident Management System (IMS), ensuring it enables the safe, effective and compliant management of patient safety events. Working closely with clinical teams, governance leads, IT colleagues and external stakeholders, you will help ensure the system aligns with operational requirements and national healthcare frameworks, including PSIRF, LFPSE and MHSDS. You will act as a vital link between technology and clinical practice, translating clinical, operational and regulatory requirements into clear and actionable system improvements. By engaging with users across the organisation, you will identify opportunities to enhance system performance, improve user experience and support the ongoing development of incident reporting processes. A key aspect of the role involves monitoring system usage, reviewing performance data and analysing feedback to identify trends and areas for improvement. You will develop and maintain reporting dashboards, produce meaningful insights and support the creation of KPIs that help track incident trends, reporting quality, system effectiveness and user engagement. **Leadership** **Key Accountabilities:** * Maintain a prioritised backlog/enhancement requests, ensuring features align with business goals and regulatory obligations. **Clinical \& Operational Alignment** * Collaborate with clinical and operational leaders to ensure the IMS supports real\-world patient safety processes. * Ensure usability for frontline staff and integration with investigation workflows such as RCA, After Action Reviews, and Learning from Deaths. **Regulatory Reporting \& Compliance** * Ensure the system meets NHS requirements, including compliance with the Patient Safety Incident Response Framework (PSIRF). * Lead the implementation and maintenance of integration with LFPSE (Learn from Patient Safety Events) platform, including automated data submission and classification standards. **IT \& System Integration** * Work with IT and development teams to ensure secure, scalable architecture. * Oversee integrations with Electronic Health Record (EHR) systems, reporting tools, and identity management (e.g., Active Directory). * Work within an ITIL framework by aligning product value delivery with IT service management processes, ensuring service stability, compliance and quality are maintained. * Embed security by design principles within all application lifecycle activities, ensuring alignment with organisational cyber security standards and regulatory compliance requirements, and actively partnering with Information Security to manage risk effectively. * Add to this re IT lifecycle management activities. **Vendor Management** * Act as a point of contact on a day\-to\-day perspective, overseeing tickets raised, vendor performance against agreed targets and SLAs. * Support service delivery review meetings. * Understand and educate vendor proposed releases/developments and ensure third parties work with EHC change enablement policy. * Stakeholder Engagement \& Business Change Management * Act as the voice of users across clinical, IT, and compliance teams. * Lead workshops, user testing, and support training team to support successful adoption. * Manage stakeholder expectations and ensure alignment with digital strategies. **To Be Successful In This Role, You Will Need** * Working knowledge of product improvements, including backlog/enhancement management, roadmap development and the ability to prioritise * Working knowledge of patient safety processes (e.g., PSIRF, Duty of Candour, incident investigation) * Understanding of LFPSE requirements and NHS data standards * Familiarity with EHR systems (e.g. Carenotes, Epic), API integration, system security, data governance and ITIL framework * Ability to use BI tools (e.g., Power BI, Tableau, Qlik) for incident trends, RCA tracking, and learning outcomes (D) * Able to align product development with real\-world frontline challenges * Can translate clinical requirements into system features and vice versa * Understands the importance of compliance and accurate safety data * Able to build strong relationships across clinical, IT, and governance teams * Delivers high\-quality, secure, and audit\-ready solutions * Balances short\-term fixes with long\-term system improvements * Standards: HL7, FHIR, SNOMED CT (useful for integration and data structure) (D) **Experience** * Experience as a Product Owner or similar role in a healthcare or regulatory\-compliant environment * Demonstrated experience working with clinical, operational and IT teams in a healthcare setting * Experience gathering requirements, conducting user testing and iterating based on feedback * Proven track record of delivering digital products that support compliance, safety and end\-user adoption * Experience with regulatory reporting and governance frameworks (e.g. PSIRF, LFPSE, CQC, NHSEI) * Experience with Incident Management Systems: RLDatix, Radar Healthcare, Ulysses (D) * Experience with NHS Reporting: LFPSE integration, NHS Digital APIs (D) **What You’ll Get** At Elysium Healthcare, we believe in taking care of the people who care for others, you’ll enjoy a comprehensive benefits package designed to support your wellbeing, growth, and future: * Annual base salary of £42,500 * The equivalent of 33 days annual leave (including bank holidays) – plus your birthday off and the option to buy additional annual leave, in our annual selection window. * Career development and training to help you achieve your professional goals * Access to our Rewards \& Benefits platform Ely\-Vate; Your one\-stop destination for everyday savings, exclusive benefits, and wellbeing hub! * Wellbeing support and activities to help you maintain a healthy work\-life balance * Access to Blue Light Card, which provides a range of exclusive offers and discounts * Life Assurance, for added peace of mind * Stream – instant access to earned wages when you need it, plus access to save, directly from your wages, alongside financial wellbeing support. * 24/7 GP service and second medical opinion, to ensure you are the best you can be * Enhanced Maternity Package, so you can truly enjoy this special time * Pension contribution, to help secure your future **About Us** Elysium Health care has over 8,000 employees and a unique approach to the delivery of care. With a network of over 80 services across England and Wales covering Mental Health, Neurological, Learning Disabilities \& Autism, Children \& Education, there is opportunity for you to grow and move. Elysium Healthcare is part of Ramsay Health Care with a global network that extends across 10 countries and employs over 86,000 people globally. *Elysium Healthcare follows safer recruitment of staff for all appointments and is a Disability Confident employer, committed to inclusive and accessible recruitment. It is a requirement that all staff understand it is each person’s individual responsibility to promote and safeguard the welfare of service users. All candidates will be subject to a DBS disclosure* \#Elysium

Pharma & Biotech
Isomorphic Labs logo

ML Research Engineer, London

Isomorphic Labs

London, England, UK

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life\-changing medicines with an ambition to solve all disease. The future is coming. A future enabled and enriched by the incredible power of machine learning. A future in which diseases are curtailed or cured starting with better and faster drug discovery. Come and be part of an interdisciplinary team driving groundbreaking innovation and play a meaningful role in contributing towards us achieving our ambitious goals, while being a part of an inspiring and collaborative culture. The world we want tomorrow is the one we’re building today. It starts with the culture at this company. It starts with you. **About Iso** Isomorphic Labs (IsoLabs) was launched in 2021 to advance human health by building on and beyond the Nobel\-winning AlphaFold system. Since then, our interdisciplinary team of drug discovery experts and machine learning specialists has built powerful new predictive and generative AI models that accelerate scientific discovery at digital speed. Our name comes from the belief that there is an underlying symmetry between biology and information science. By harnessing AI’s powerful capabilities, we can use it to model complex biological phenomena to help design novel molecules, anticipate how drugs will perform and develop innovative medicines to treat and cure some of the world’s most devastating diseases. We have built a world\-leading drug design engine comprising AI models that are capable of working across multiple therapeutic areas and drug modalities. We are continually innovating on model architecture and developing cutting\-edge capabilities to advance rational drug design. Every day, and with each new breakthrough, we’re getting closer to the promise of digital biology, and achieving our ambitious mission to one day solve all disease with the help of AI. **Research Engineering (Machine Learning), London** **We are looking for Research Engineers with different levels of experience \- Mid through to Senior, Staff, Principal or equivalent levels.** **Your impact** This is an exciting opportunity for you to contribute to frontier research at the intersection of AI and drug design. Working in a highly creative, iterative environment, you will be partnering with scientists and engineers to advance foundational models that will transform the biopharmaceutical world as we know it. You will draw upon your existing engineering and Machine Learning experience whilst learning from those around you, to apply novel techniques and ideas to newly encountered computational biology and chemistry problems. **What You Will Do** **Implementation \& Optimisation:** * Translate research concepts into practical implementations by developing and optimising state\-of\-the\-art AI models, and building and maintaining robust codebases, data pipelines, and infrastructure for training and evaluation. **Experimentation \& Evaluation:** * Design, implement, and run experiments to evaluate the performance and robustness of ML models, using a full spectrum of state\-of\-the\-art machine learning methods. Evaluating, tuning, and maintaining AI/ML models (which includes collecting and preparing data as needed) **Evaluation \& Inference:** * Implement algorithms and software to analyse and evaluate the performance of AI models. * Optimising performance of AI/ML models such as Diffusion models, Transformers, GNNs, leveraging a deep understanding of the AI/ML hardware\+software stack * Advise on how to bring AI/ML models to production and/or integrating them into product offerings, and monitoring and refining their behavior. * Developing specialised tools/frameworks/infrastructure to aid in the work above **Collaboration \& Knowledge Sharing:** * Work closely with research scientists and engineers, contributing to team discussions, sharing knowledge, and actively participating in code reviews to foster a collaborative environment. **Innovation \& Impact:** * Proactively identify and address technical challenges, stay updated on the latest AI advancements, and focus on developing solutions that enable scaling our wider foundation and applied model platforms. * Ability to execute on independent engineering projects and software development towards research goals. **Essential** **Skills and Qualifications** * Academic Background: Advanced degree (Master’s or PhD) in a highly quantitative field (Computer Science, AI, Physics, Mathematics, etc.) or equivalent practical experience. * ML Fundamentals: Deep understanding of machine learning principles and techniques. * Framework Expertise: Strong proficiency in deep learning frameworks such as JAX or PyTorch. * Modern Architectures: Hands\-on experience building and working with modern model architectures (e.g., Transformers, GNNs, Diffusion Models). * Full ML Lifecycle: Experience taking models from conception to production (scoping, data analysis, training, debugging, evaluation, benchmarking, and deployment). * Engineering Excellence: Excellent software development skills with strong algorithms and data structures fundamentals. * Collaboration \& Communication: An excellent team player with strong written and verbal communication skills, able to collaborate seamlessly in a cross\-disciplinary environment. * Agency: Self\-directed with an ability to navigate ambiguity, propose and own complex projects, learn the necessary context, and readily adapt to new domains and developments. **Nice to have** * Proven Research Record: A history of scientific contributions (e.g., publications at NeurIPS, ICML, ICLR, CVPR) or significant contributions to state\-of\-the\-art AI models. * Scale \& Performance: Experience training models across distributed systems (multi\-GPU/multi\-node) and optimising training and inference performance (e.g., XLA, Triton, CUDA, Pallas). * Domain Knowledge: A strong interest in, or knowledge of, biochemistry, computational biology, or drug discovery fundamentals. * Industry Experience: Proven track record working in reputable tech companies or research labs. * Applied ML: Experience developing models developed for real\-world applications. * Infrastructure: Solid technical infrastructure knowledge and experience with low\-level engineering (e.g., GCP, Kubernetes, Docker) **Culture and values** We are guided by our shared values. It's not about finding people who think and act in the same way. These values help to guide our work and will continue to strengthen it. **Thoughtful** Thoughtful at Iso is about curiosity, creativity and care. It is about good people doing good, rigorous and future\-making science every single day. **Brave** Brave at Iso is about fearlessness, but it’s also about initiative and integrity. The scale of the challenge demands nothing less. **Determined** Determined at Iso is the way we pursue our goal. It’s a confidence in our hypothesis, as well as the urgency and agility needed to deliver on it. Because disease won’t wait, so neither should we. **Together** Together at Iso is about connection, collaboration across fields and catalytic relationships. It’s knowing that transformation is a group project, and remembering that what we’re doing will have a real impact on real people everywhere. **Creating An Extraordinary Company** We believe that to be successful we need a team with a range of skills and talents. We're building an environment where collaboration is fundamental, learning is shared and every employee feels supported and able to thrive. We value unique experiences, knowledge, backgrounds, and perspectives, and harness these qualities to create extraordinary impact. We are committed to equal employment opportunities regardless of sex, race, religion or belief, ethnic or national origin, disability, age, citizenship, marital, domestic or civil partnership status, sexual orientation, gender identity, pregnancy or related condition (including breastfeeding) or any other basis protected by applicable law. If you have a disability or additional need that requires accommodation, please do not hesitate to let us know. **Hybrid working** It’s hugely important for us to share knowledge and build strong relationships with each other, and we find it easier to do this if we spend time together in person. This is why we follow a hybrid model, and **would require you to be able to come into the office 3 days a week** (currently Tuesday, Wednesday, and one other day depending on which team you’re in). If you have additional needs that would prevent you from following this hybrid approach, we’d be happy to talk through these if you’re selected for an initial screening call. **Please note that when you submit an application, your data will be processed in line with our privacy policy.** \>\> Click to view other open roles at Isomorphic Labs

Healthtech & Digital Health
Hologic, Inc. logo

Gynaecology Surgical Solutions Pathway Specialist - South UK

Hologic, Inc.

Manchester, England, UK

At Hologic, we are driven by a powerful purpose: enabling healthier lives everywhere, every day. Through The Science of Sure, we advance women’s health with innovative solutions that help healthcare providers improve access, efficiency and patient outcomes. We are looking for a Pathway Specialist to join our UK \& Ireland Gynaecological Surgical Solutions \& Sonata team, covering the South of the UK, with a primary focus from the Midlands through to North London. This strategic, field\-based role is focused on engaging senior NHS and private healthcare leaders to shape women’s health pathways, support service transformation and drive adoption of Hologic’s GSSS solutions. Working closely with Surgical Sales Specialists and cross\-functional teams, you will build senior\-level partnerships, present compelling clinical and commercial value propositions, and help make the case for improved access to minimally invasive treatment options for women. **What To Expect** * Build and maintain strategic relationships with senior healthcare leaders across NHS Trusts, ICBs, PCNs, commissioning bodies and private healthcare organisations. * Present compelling clinical, commercial and health economic value propositions that align Hologic’s GSSS offering to customer priorities. * Partner closely with Surgical Sales Specialists to create senior\-level engagement, understanding and buy\-in for Hologic’s surgical solutions. * Identify pathway and service delivery gaps, supporting opportunities to improve patient access, referral routes and treatment efficiency. * Lead senior\-level commercial discussions from early engagement through to contract negotiation, in collaboration with internal stakeholders. * Develop a strong network of healthcare decision makers and KOLs across the region. * Identify and shape opportunities for growth, including upsell, cross\-sell, contract extension and site\-of\-service expansion. * Collaborate cross\-functionally with Sales, Service, Finance, Legal, Operations, Marketing and Education teams to design strong customer solutions. * Maintain accurate customer and account insight through CRM and site profiling tools. * Travel regularly across the region, with expected travel averaging 70–80% of working time, including overnight stays. **What We Expect** * Experience engaging and influencing senior healthcare stakeholders, ideally within the NHS, private healthcare or medical technology sectors. * Strong understanding of NHS structures, commissioning processes, Integrated Care Boards and healthcare decision\-making pathways. * Commercial acumen, with the ability to present business cases, lead strategic discussions and support contract negotiations. * Passion for women’s health and the ability to communicate the value of improved pathways and minimally invasive treatment options. * Strong relationship\-building, networking, negotiation and influencing skills. * Ability to translate complex clinical, financial and performance data into clear, insight\-led recommendations. * A proactive, resilient and results\-oriented approach, with the ability to drive outcomes through influence and collaboration. * Confidence using CRM systems, sales enablement tools and standard office productivity software. * A current valid driving licence. * Fluent English language skills. Additional local or European languages are beneficial but not essential. **Why Hologic?** * Work for a company dedicated to advancing women’s health and improving lives through innovative healthcare solutions. * Play a strategic role in shaping women’s health pathways and supporting system\-level change across the UK. * Develop your career within a global organisation committed to innovation, quality, ethics and meaningful impact. Salary: £42,000 – £55,000 gross pa base \+ commission (OTE £63,000 – £82,500 based on target performance, with opportunity to earn greater than OTE for those who exceed their targets). The final offer will depend on experience, skills, and alignment with internal pay structures. In addition, we offer a comprehensive benefits package including pension and insurances. **Apply Today to Join Our Team and Make a Difference!**

Medical Device
Novartis UK logo

Global Labelling Manager, Content (Neuroscience)

Novartis UK

The Home, United Kingdom

**Summary** Location: London, United Kingdom Remote (For those residing in the UK, but more than 50 miles from the office) Relocation Support: This role is based in London (The Westworks), United Kingdom or Remote. Novartis is unable to offer relocation support: please only apply if accessible. Imagine shaping the information that helps healthcare professionals and patients make informed treatment decisions around the world. As Global Labelling Manager, Content (Neuroscience), you will play a pivotal role in developing clear, accurate, and compliant product labelling that supports innovative neuroscience medicines across global markets. Working at the intersection of science, regulation, and strategy, you will collaborate with cross\-functional experts to translate complex clinical and safety data into impactful product information, helping ensure that patients have access to trusted medicines while driving excellence in global labelling practices. **About The Role** **Key Responsibilities** * Lead development and maintenance of global labelling documents for assigned neuroscience products. * Prepare high\-quality labelling content aligned with global regulatory requirements and product strategy. * Facilitate cross\-functional labelling discussions and drive alignment on content decisions and implementation plans. * Evaluate clinical, safety and competitor data to support evidence\-based labelling updates. * Support responses to Health Authority enquiries with accurate, well\-documented labelling information. * Ensure timely implementation of approved labelling changes across global and major market labels. * Maintain robust documentation, traceability and version control to support audit readiness and compliance. **Essential Requirements** * Degree in a scientific discipline or equivalent experience within the pharmaceutical industry. * Experience developing, reviewing or maintaining regulatory or labelling content for medicinal products. * Strong understanding of global labelling principles and major market labelling requirements. * Ability to interpret clinical and safety data and translate findings into clear product information. * Excellent collaboration, communication and stakeholder management skills across cross\-functional teams. * Strong attention to detail with a focus on quality, compliance and documentation accuracy. **Benefits \& Rewards** At Novartis, we’re committed to reimagining medicine together \- and rewarding the people who make it happen. **Expected Annual Base Salary Range for role: £56,511 to £104,949** The base salary offered is determined based on gender\-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance\-based bonus depending on certain performance parameters. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. You may be eligible for a company vehicle or a car allowance in accordance with the applicable local Novartis policies and guidelines. Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis\_com/files/novartis\-life\-handbook.pdf *Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.* **Commitment to Diversity and Inclusion / EEO paragraph** Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve. **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Benefits and Rewards:** Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Pharma & Biotech
Fifth Dimension logo

Founding Growth Lead, London

Fifth Dimension

London, England, UK

**About Us** The real\-assets industry runs on fragmented systems, disconnected data and a huge amount of manual work. At Fifth Dimension, we’re building the decision intelligence platform for real\-assets investors and managers, helping teams move faster, surface better insight and make more confident investment decisions. We’ve recently raised a $26M Series A led by HV Capital and are expanding across the US and APAC. Now we’re hiring our first dedicated Growth Lead. Not to ‘run marketing’. To help us figure out how enterprise growth should actually work here. We’re at the stage where there’s real momentum, but still plenty to build. We’re looking for someone who enjoys creating structure, improving systems and helping turn early GTM signals into a more scalable growth engine. ****What is the role?**** We’re looking for a hands\-on, highly analytical and highly executional Growth Lead to help us build and scale our enterprise demand generation motion. You’ll work across outbound, nurture, events, lifecycle, growth experimentation and experimenting with ABM growth tactics to help us reach the right enterprise buyers in the right way. You’ll partner closely with sales to build repeatable systems, improve funnel visibility and help define what scalable pipeline generation should look like at Fifth Dimension. This is a great role for someone who enjoys building from the ground up. We have momentum, customers and a clear market opportunity, but we’re still early in how our growth function operates. You’ll be joining at the stage where there is plenty to figure out and improve. You’ll need to be comfortable switching between strategy and execution, and genuinely skilled at translating strategy into an executable plan. You understand how individual tactics fit within a larger strategic framework, no random acts of marketing. One day you might be mapping nurture journeys in HubSpot. The next, you might be analysing funnel conversion data, refining outbound logic, improving event follow\-up or helping shape GTM priorities. You’ll have built strong marketing foundations the traditional way, and you now know how to set up AI workflows that deliver real efficiency, with the right human oversight to maintain quality. We care far more about ownership, operational thinking and execution than polished corporate marketing playbooks. We don’t believe channels should be fixed in advance. This is a Growth role: we’d expect you to bring hypotheses, run experiments and use whatever channel mix proves most effective, rather than being constrained by a predefined playbook. Frameworks like Crossing the Chasm are useful and there are real lessons to take from them, but they aren’t the only lens on our market. We’re cautious about assuming traditional technology adoption models map neatly onto AI adoption, so we want someone who brings experience and frameworks but is equally willing to test assumptions and adapt based on what they’re seeing in the market. ****What you’ll do**** * Build and improve outbound and nurture workflows across email, LinkedIn, events and engagement\-triggered campaigns * Help create a more repeatable enterprise pipeline engine * Own and optimise growth workflows in HubSpot, including account\-level insight and data management * Design, run and measure growth experiments across channels, using the mix that proves most effective * Form hypotheses on the best ABM strategies for our ICPs, run the tests, report the results and iterate the approach * Improve targeting, sequencing and conversion across the funnel * Build clearer reporting and visibility across growth performance * Work closely with SDRs and sales to improve lead quality and follow\-up * Engage and track the buying group, developing the messaging and content that moves multiple stakeholders down the funnel * Partner with leadership on growth priorities, channel performance and GTM rhythm * Bring more structure and operational rigour to how we generate demand * Help shape what the growth function becomes as the company scales ****What we’re looking for**** ****You’ve probably:**** * Spent 6\+ years in B2B SaaS growth, demand generation or GTM operations * Worked in early\-stage or scaling companies before * Helped build something from 0–1 or 0\.5–1 (at least once) * Worked closely with enterprise sales teams * Built workflows and campaigns yourself rather than only managing agencies * Built strong marketing foundations the traditional way, and since learned to set up AI workflows with the right guardrails and human oversight * Used HubSpot heavily and understand how funnels, workflows and reporting connect, including configuring it to harvest account\-level insight * Run account\-based marketing: engaging and tracking the buying group, and developing multithreaded conversations across a complex buying committee * Experience setting up, testing and iterating ABM strategies with hands\-on execution * Operated in environments where priorities change quickly and structure is still evolving ****You’re probably someone who:**** * Thinks in systems and metrics * Likes solving operational problems * Owns it, you see a problem and take responsibility for solving it * Ships it, you value momentum, execution and learning through action * Is comfortable with ambiguity * Doesn’t wait to be told exactly what to do * Enjoys working cross\-functionally * Cares more about outcomes than optics * Doesn’t do boring, you challenge the status quo, bring original ideas and make things better than you found them ****Bonus points for experience in:**** * PropTech * Real Estate ****This role may not be for you if…**** * You prefer larger, more mature marketing teams with established playbooks * You enjoy strategy more than execution * You need lots of structure around you to operate well * You optimise for perfection over momentum (one of our values is ‘Ship it’!) * You’re a paid media specialist looking for a channel\-specific role rather than a broad growth mandate * You want a narrow role with highly defined boundaries **Compensation** * £110,000\-130,000 \+ bonus

Healthtech & Digital Health
STADA Thornton & Ross logo

Senior Category Manager

STADA Thornton & Ross

Reading, England, UK

STADA UK Thornton \& Ross is on an exciting growth journey with more than 700 employees being fully committed to our purpose of Caring for People’s Health as a Trusted Partner. Together we are shaping the future of Thornton \& Ross by living our values of Integrity, Entrepreneurship, Agility and One STADA. If you want to work in an open culture where your uniqueness is valued, **join our CHC Insights Team** . **STADA UK Thornton \& Ross – Senior Category Manager** **Reading \|U.K.\| Full\-time \| Permanent** **Role Purpose** The Senior Category Manager will join STADA UK Thornton \& Ross at a time of strong momentum, portfolio expansion, and organisational transformation. This is an exciting opportunity to play a key role in accelerating the growth of our Consumer Health brands by driving category leadership, strengthening customer partnerships, and improving execution across in\-market activity. You will develop and lead category partnerships with key customers, drive category growth, enhance Thornton \& Ross brand visibility, and increase share of distribution across channels. **How You Will Make Impact** **1\) Build \& Lead Strategic Category Partnerships** Establish And Independently Manage Strong Category Relationships With Key Customers, Ensuring Regular Engagement Supported By Objective Market And Competitor Insights. Deliver Clear, Commercially Focused Recommendations That Drive Action Across * Range reviews and assortment optimisation * Different retail and store formats * Online and e\-commerce environments * Trade and promotional planning Ensure insights are translated into actionable strategies that influence customer decisions and category growth. **2\) Build Category \& Shopper Insight Advantage** Create a competitive advantage for Thornton \& Ross by developing best\-in\-class category and shopper insight for key customers. Shape and adapt the insight agenda to meet both customer and category needs, including loyalty card data, shopper behaviour, and purchase drivers. Develop efficient processes for regular, timely insight delivery and continuously evaluate the ROI of insight investment across customers and categories. **3\)** **Define \& Drive Category Performance Metrics** Define, set, and track category KPIs and performance objectives across all key customers and brands, including: * Category and brand growth vs market * Thornton \& Ross share of distribution * In\-store and online brand visibility Integrate EPOS, category, and shopper data with detailed range and planogram analysis across retail formats to build a holistic view of performance. Share insights internally and collaborate cross\-functionally to drive continuous improvement. **4\)** **Influence Customers Through Insight\-Led Storytelling** Develop and deliver compelling category narratives that shape customer thinking around shopper needs and market opportunities. Influence key stakeholders by: * Presenting clear, insight\-led category recommendations * Demonstrating “what good looks like” in\-store and online * Building impactful visual merchandising concepts and planograms * Translating data into engaging, actionable stories that drive change **5\)** **Drive T\&R Commercial \& Customer Initiatives** Support the delivery of Thornton \& Ross commercial priorities, including channel strategy and sales objectives. Work closely with Account Managers to maximise category opportunities and leverage strong customer relationships to support overall business growth. **What We Are Looking For** At STADA UK Thornton \& Ross, we embrace Uniqueness—recognising the value that diverse perspectives bring to our work. Our core values—Entrepreneurship, Integrity, Agility, and One STADA—guide how we collaborate and innovate. We are looking for a candidate who aligns with these values and brings the following: * University degree in Marketing, Business, Communications, or a related field (preferred) * Experience in FMCG, Consumer Health, or a fast\-paced commercial environment * Strong drive, ambition, and results\-oriented mindset * High adaptability and ability to thrive in change * Strong numerical and analytical capability * Excellent organisational skills with strong attention to detail * High energy, proactive approach, and eagerness to learn and develop * Strong communication and cross\-functional collaboration skills **How We Care For You** At Thornton \& Ross our purpose “Caring for people’s health as a trusted partner” motivates us every day. And what would be a better place than starting with our own employees. Which is why we give much in return: 💸 Competitive salary and annual bonus scheme. 🗝 Salary Sacrifice Pension Scheme offering 6% employer contribution rates. ⌚ Hybrid working – we spend three days of your choice in the office, with the remaining days working at home. 🌴 25 days of annual leave plus bank holidays with the potential to buy up to 5 additional days. 💉 Free winter flu jab. 🧠 Wellbeing support through our Employee Assistance Programme and KYAN Wellbeing – offering free coaching and counselling services for you and your family. ⚡ Electric Car Scheme through Octopus Energy, plus free on\-site EV charging. 🚲 Cycle to Work Scheme. 👪 Enhanced Family Leave. 🎉 Plus, many more employee benefits \& celebration events. *STADA Group values and promotes its diverse culture, regardless of gender, age, social or ethnic origin, disabilities, religion, ideology, or sexual orientation. We use the strength of our uniqueness to develop creative ideas, expand our experience and increase innovative strength. Our focus is on equal opportunities, respectful cooperation, and the promotion of an inclusive working environment. We are looking forward to your application and welcome applications without a pharmaceutical background.*

Pharma & Biotech
OPEN Health logo

Medical Writer - Publications & Medical Communications

OPEN Health

Location not specified

**Medical Writer** Reports to the Senior or Principal Medical Writer **Job Summary** Medical content development encompasses a range of deliverables including strategy/ planning, publications, posters, manuscripts, and interactive content. This is a fantastic role, working with on a team that partners with a growing portfolio of leading pharma clients across oncology as a therapeutic area. **Essential Duties \& Responsibilities** * Ensuring that quality control is paramount within all materials produced across the business * Developing written materials (for subsequent review by Lead / Senior Medical Writer) in line with client requirements (internal/external), timelines, Open Health Medical Communications editorial policy, ABPI Code of Practice and key product messages * May include editing as well as writing * Ensuring all written material is: * Appropriately pitched * On brief when delivered * Delivered on time * Fully referenced and, where applicable, abides by the ABPI Code of Practice * Attending meetings with Lead / Senior Medical Writer and developing first draft of report for review * Coordinating effectively and efficiently with appropriate members of the Open Health Medical Communications team * Ensuring line manager and accounts team, where appropriate, are continually updated on project progress * Developing an understanding of the various client brand and disease areas * Undertaking or directing research into therapy areas, as needed * Liaising with authors / advisors (including attending face\-to\-face meetings), with the support of a Lead / Senior Medical Writer **Experience, Skills, And Qualifications** * Experience as a Medical Writer in a medcomms, healthcare agency or pharma environment * Thorough understanding of the client’s therapeutic area and ability to provide strategic input * Strong understanding of science and medicine, the healthcare environment and the medical education/communications industry * Manager, trainer, delegator * Strong leadership skills * Approachability * Significant experience in a healthcare agency or pharmaceutical company role * Excellent project management and analytical skills * Financial acumen * Ability to multitask and prioritise; excellent time management skills * Excellent written and verbal communication and interpersonal skills * Attention to detail * Able to work independently and as part of a team * Competent in Microsoft Word, PowerPoint, Excel and Outlook * Sound understanding of the ABPI Code of Practice Travel Requirements * As required by business needs

Pharma & Biotech
Newton logo

Principal Consultant - Health and Local Government

Newton

London, England, UK

We are excited about the future of public services, and partner with health and local authorities to deliver meaningful transformation at pace that has a tangible positive impact on the people they serve. Our consulting teams work at the heart of public services to improve experiences and outcomes for people, and reduce spend by delivering the right care in the right place. We will be typically working on either an intense diagnostic or on multi\-year, multi\-million\-pound transformation programmes with the guarantee of a delivery outcome to our clients. This can be for example building new services and ways of working, improving hospital flow, improving care pathways to maximise independence, or making the shift to proactive preventative approaches. It is crucial that we understand the client fully to identify the biggest opportunity for improvement, design the right solutions and work hand\-in\-hand with the client to implement these in a way that is sustainable. We work where our client works which can often mean working away from home during the week. As a **Principal Consultant** in Newton, you will be leading your client and team through complex delivery transformation with accountability for delivering a significant value to the client which could be \~£5m. You will be typically managing a team of multi\-disciplined consultants across multiple workstreams. You will have been building your presence as a leader in your current organisation, putting significant effort into developing your team and starting to develop your business development skills through things like spotting opportunities for future work. The role is incredibly varied but would typically cover, but not be limited to: * For a large part of a programme or a small engagement, you will be managing a larger team (up to 8\) including matrix management, designing the workstreams (alongside your line manager) that your Lead Consultants and below will deliver, leading senior clients and sponsors on a journey, seeking to assure them of project progress and achieving full client satisfaction * Leading on programme governance including reporting, risk/issue/decision management and stakeholder engagement including managing upwards and escalating risks * Starting to own part of an account plan and working with other programme leads to define outcomes for connected workstreams as a part of a wider programme * Steering your team on the analysis and modelling that needs to happen to identify and/or deliver the opportunity and leading them to create a compelling data\-driven narrative at a programme and organisation\-wide level and then supporting them with presenting this to the senior client * Proactively leaning in to develop your teams, considering their long\-term career aspirations and development goals and how you can best support them * Proactively identifying how your project team can contribute to wider market and account engagement activities and progressing this ‘side of desk' in support of your account leadership team Successful recruitment will see you hired into our Public Cluster. During your onboarding the cluster will commit to scheduling you into the right client programmes with the right support to adapt to Newton's core approach to programme delivery. Once you are fully onboarded there will be opportunities to work more broadly across our other markets in line with business needs. **Requirements** A Principal Consultant in Newton is likely to be a top end Manager or early Senior Manager in another consulting firm (or equivalent titles), leading a large part of a programme or having overall delivery responsibility of a small client engagement. We Will Be Looking For Demonstrable Experience In Delivering Multiple Operational Transformation And Improvement Projects Which Have Delivered Tangible, Measurable Outcomes Across Any Of The Following Markets * Health services * Local government * Central Government It is crucial to have the following skills and attributes to be successful in this role: * Managing teams of consultants of various levels, capability areas and across different workstreams * Building and maintaining trusted relationships with senior managers, heads of function or programme, with competence and confidence to present in front of client executives * Purpose led analysis skills and ability to use logic to solve a problem * Ability to compellingly present assessment and programme outputs to enable successful progression of next steps * Running day to day internal and client facing governance * Resilience in solving highly complex problems * Collaborative nature, working with internal and external teams to get to the best outcome together * Proven track record for driving improvement or impact with an outcome focussed mindset * Big picture thinking and the ability to connect the dots using relevant market themes * Starting to think more commercially by spotting potential opportunities and understanding and communicating potential risks * Willingness for self\-development and commitment to supporting the development of others around you; actively seeks and gives feedback * Ambitious and driven; always strives for the best outcomes for self and others * Flexible and willing to work away from home **Benefits** Supporting you starts from day one. New joiners often highlight the Newton energy and support they first encounter in the recruitment process and that continues through into their time at Newton. Once in role, you'll get support from several sources \- from stretching projects, on\-the\-job feedback and developmental guidance from Directors and Partners. You'll have a dedicated and consistent Sponsor/Development Manager to support your career progression with promotions at Newton happening throughout the year and based on performance and readiness to perform and succeed at the next level. You'll receive regular appraisals and annual pay reviews. We offer a highly competitive salary, standardised sign\-on bonus and our generous benefits package includes car allowance, life assurance, income protection, pension contributions and 29 days holiday (not including bank holidays). We also operate profit share and equity schemes so that our people share in the success of the business. The profit share bonus is based on company performance and typically paid out in March and September. Joining us also brings many social benefits. We have a full social calendar with Spring activity days, Christmas events, a 2\-day Summer event and 4 Newton\-sponsored weekends a year.

Healthtech & Digital Health
Moderna logo

Associate Director, CMC Regulatory Affairs, International

Moderna

London, England, UK

**The Role** Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its presence in London, a global center of science and innovation. Our team drives commercial operations to bring our mRNA medicines to patients across the UK. We welcome talent ready to help transform global health. This is an opportunity for an experienced CMC Regulatory Affairs professional to play a critical role in advancing Moderna’s global product portfolio. This pivotal role will focus on preparing and overseeing CMC and Quality related agency correspondence and regulatory applications, governing CMC submissions, and providing regulatory compliance support for the development of global products. The successful candidate will lead and support all regulatory activities, ensuring the delivery of high\-quality CMC sections of regulatory documentation. This role demands a dynamic individual capable of managing multiple projects in a fast and results\-oriented environment, dedicated to bringing a new generation of transformative medicines to patients. **Here’s What You’ll Do** * Develop and implement effective global CMC regulatory strategies for international submissions, including INDs, CTAs, BLAs, MAAs, and other regional regulatory applications. * Lead the preparation, review, and oversight of CMC and Quality\-related agency correspondence and regulatory submissions. * Govern and coordinate CMC submission activities to ensure alignment with global regulatory requirements and business objectives. * Identify, assess, and proactively mitigate regulatory risks impacting product development, lifecycle management, and market access activities. * Provide strategic CMC regulatory guidance to cross\-functional product development teams throughout the product lifecycle. * Review regulatory documentation for submission readiness, ensuring compliance with applicable health authority requirements, regulations, and guidance. * Lead CMC regulatory discussions, negotiations, and interactions with international health authorities to facilitate efficient review and approval of submissions. * Develop, implement, and continuously improve regulatory processes and procedures supporting CMC components of global regulatory filings. * Support the creation, maintenance, and optimization of CMC submission templates and associated regulatory documentation standards. * Partner closely with Manufacturing, Technical Operations, Quality, and Development teams to provide regulatory guidance on CMC\-related matters. * Evaluate CMC change controls and provide regulatory assessments to support implementation strategies and compliance requirements. * Interpret evolving regulatory guidance documents, regulations, directives, and policy changes, advising internal stakeholders on their applicability and impact. * Provide regulatory compliance support across global development and commercial programs. * Lead regulatory oversight of multiple programs spanning vaccines, oncology, and rare disease therapeutic areas. * Support lifecycle management activities for approved and post\-approval biologic products across international markets. * Contribute to regulatory planning and execution across emerging markets, with particular emphasis on LATAM regulatory environments. * Leverage digital technologies and emerging AI\-enabled capabilities to enhance regulatory intelligence, submission planning, data management, and operational efficiency. * Operate effectively in a fast\-paced, highly collaborative environment while managing multiple complex projects and competing priorities. **The key Moderna Mindsets you’ll need to succeed in the role** * Pursue options in parallel: This role requires a strategic thinker who can explore multiple avenues simultaneously to ensure the most efficient and effective regulatory strategies. * Act with urgency: Given the fast\-paced and result\-oriented environment, acting swiftly and decisively is crucial to meet deadlines and deliver transformative medicines to patients. **Here’s What You’ll Need (Basic Qualifications)** * BS in Pharmaceutics, Chemistry, Chemical Engineering, or closely related field is required. * MS degree in Pharmaceutics, Chemistry, Chemical Engineering, or closely related field is desirable * 10\+ years of experience in the pharmaceutical/biotech industry, manufacturing and/or analytical focus * 8\+ years of experience in Biologics focused Regulatory CMC * Multidisciplinary focus on certain therapeutic areas (vaccines, oncology and/or rare diseases) + Strong knowledge of current EU and ROW regulations + Strong knowledge of Cgmp + Strong experience with CTD format and content regulatory filings + Exceptional written and oral communication **Pay \& Benefits** **At Moderna, we believe that when you feel your best, you can do your best work. That’s why our global benefits and well\-being resources are designed to support you—at work, at home, and everywhere in between.** * Best\-in\-class healthcare, plus voluntary benefit programs to support your unique needs * A holistic approach to well\-being with access to fitness, mindfulness, and mental health support * Family building benefits, including fertility, adoption, and surrogacy support * Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year\-end shutdown * Savings and investments to help you plan for the future * Location\-specific perks and extras The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work. **About Moderna** Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world\-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities. We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. As we build our company, we have always believed an in\-person culture is critical to our success. Moderna champions the significant benefits of in\-office collaboration by embracing a 70/30 work model. This 70% in\-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Moderna is a smoke\-free, alcohol\-free, and drug\-free work environment. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply! Moderna is committed to equal opportunity in employment and non\-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best. Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at leavesandaccommodations@modernatx.com.

Pharma & Biotech
Newton logo

Lead Consultant - Health and Local Government

Newton

London, England, UK

We are excited about the future of public services, and partner with health and local authorities to deliver meaningful transformation at pace that has a tangible positive impact on the people they serve. Our consulting teams work at the heart of public services to improve experiences and outcomes for people, and reduce spend by delivering the right care in the right place. We will be typically working on either an intense diagnostic or on multi\-year, multi\-million\-pound transformation programmes with the guarantee of a delivery outcome to our clients. This can be for example building new services and ways of working, improving hospital flow, improving care pathways to maximise independence, or making the shift to proactive preventative approaches. It is crucial that we understand the client fully to identify the biggest opportunity for improvement, design the right solutions and work hand\-in\-hand with the client to implement these in a way that is sustainable. We work where our client works which can often mean working away from home during the week. As a Lead Consultant, you will be responsible for the delivery of workstreams typically delivering value of \~£2m to the client. You will be designing solutions, identifying the right KPIs for yourself and your team, and driving continuous improvement. You will have productive mid\-level client relationships that help to deliver excellent results. You will be at the heart of driving results, getting the best out of both your team and the client.. The role is incredibly varied but would typically cover, but not be limited to: * Managing a small team of consultants (no more than 4\) through advanced analysis and modelling to identify the biggest opportunities, and then leading your team and client to deliver them * Reviewing the proposed design for a workstream as created by the Principal Consultant or Business Manager in your programme * Working closely with programme leads to ensure your workstream KPIs are aligned to client organisational outcomes and wider goals * Aligning your team and client to measurable KPIs through design and implementation of effective governance that embeds a culture of continuous progress review day to day that enables successful delivery * Working on site, day to day with your client counterparts to review progress and problem solve to drive performance up, directly or through your teams, building your client's capability * Creating a clear, compelling story for stakeholders \- from frontline managers to the senior managers \- and working with programme leads to develop this for the senior client stakeholders to remove blockers to progress * Proactively escalating risks, and supporting with the adjustment of resource and commercial plans to keep the programme on track Successful recruitment will see you hired into our Public Cluster. During your onboarding that chosen cluster will commit to scheduling you into the right client programmes with the right support to adapt to Newton's core approach to programme delivery. Once you are fully onboarded there will be opportunities to work more broadly across our other markets in line with business needs. **Requirements** A Lead Consultant in Newton is likely to be at the early stages of a Manager grade (or equivalent title) or progressing towards that in another consulting firm, or equivalent public sector transformation role leading part of a programme with support from a programme lead and directly managing small teams. You will be used to building and maintaining relationships with senior managers or heads of function or programme. We Will Be Looking For Demonstrable Experience In Delivering Multiple Operational Transformation And Improvement Projects With a Focus On Driving Tangible Improvement In Public Service Delivery In Any Of The Below Sectors * Health services * Local government * Central Government It is crucial to have the following skills and attributes to be successful in this role: * Building trusted relationships with clients and internal teams * Direct line management of a small team of multi\-disciplined consultants * Purpose led analysis skills and ability to use logic to solve a problem * Resilience in solving highly complex problems * Collaborative nature, working with internal and external teams to get to the best outcome together * Proven track record for driving improvement or impact with an outcome focused mindset * Willingness for self\-development and commitment to supporting the development of others around you; actively seeks and gives feedback * Ambitious and driven; always strives for the best outcomes for self and others * Flexible and willing to work away from home **Benefits** Supporting you starts from day one. New joiners often highlight the Newton energy and support they first encounter in the recruitment process and that continues through into their time at Newton. Once in role, you'll get support from several sources \- from stretching projects, on\-the\-job feedback and developmental guidance from Directors and Partners. You'll have a dedicated and consistent Sponsor/Development Manager to support your career progression with promotions at Newton happening throughout the year and based on performance and readiness to perform and succeed at the next level. You'll receive regular appraisals and annual pay reviews. We offer a highly competitive salary, a standardised sign\-on bonus and our generous benefits package includes car allowance, life assurance, income protection, pension contributions and 28 days holiday (not including bank holidays). We also operate profit share and equity schemes so that our people share in the success of the business. The profit share bonus is based on company performance and typically paid out in March and September. Joining us also brings many social benefits. We have a full social calendar with Spring activity days, Christmas events, a 2\-day Summer event and 4 Newton\-sponsored weekends a year.

Healthtech & Digital Health
Cognism logo

Website & Conversion Optimisation Manager

Cognism

London, England, UK

WHO ARE WE Cognism is the leading provider of European B2B data and sales intelligence. Ambitious businesses of every size use our platform to discover, connect, and engage with qualified decision\-makers faster and close more deals. Headquartered in London with global offices, Cognism’s contact data and contextual signals are trusted by thousands of revenue teams to eliminate the guesswork from prospecting. **OUR WORK MODEL:** **Hybrid:** This is a hybrid role, requiring you to work from our London office 3 days per week, with flexibility to work remotely on other days.   **THE ROLE:** We are looking for a Website \& Conversion Optimisation Manager to own and improve the performance of Cognism’s website as a key driver of pipeline and revenue.   The website plays a critical role in how buyers discover Cognism, understand our product and convert into opportunities. In this role, you will focus on improving the effectiveness of the site through user experience improvements, landing page optimisation and ongoing experimentation.   You will work closely with Demand Generation, Product Marketing, Paid Media and Content teams to ensure the website supports campaigns, clearly communicates our value proposition and creates a seamless journey from first visit through to conversion.   We are looking for someone who is naturally curious and highly customer\-focused. You enjoy digging into user behaviour, understanding how buyers navigate the site and identifying opportunities to improve the customer journey. Your goal is to create a best\-in\-class website experience that helps prospects quickly understand the value of Cognism and take the next step.   **THE IDEAL CANDIDATE:** * You have experience managing and optimising B2B SaaS websites and understand how websites support demand generation and pipeline growth. * You are comfortable improving website performance through conversion rate optimisation and experimentation, testing and refining landing pages, product pages and key user journeys. * You are naturally curious about user behaviour and enjoy analysing data and feedback to uncover opportunities to improve the customer experience. * You are comfortable analysing and reporting on website and funnel performance, using insights to prioritise improvements that drive better engagement and conversion. * You are customer\-focused and motivated to create intuitive journeys that help prospects quickly understand value and move smoothly through the funnel. * You combine strategic thinking with a hands\-on approach and enjoy working cross\-functionally with marketing, design and development teams to implement improvements and support wider go\-to\-market campaigns. **RESPONSIBILITIES:** * Own and manage Cognism’s website performance as a key marketing and pipeline generation asset. * Optimise landing pages, product pages and core conversion journeys across the website. * Plan and run CRO experiments to improve engagement and conversion rates. * Analyse website performance and user behaviour to identify opportunities for improvement. * Work closely with Demand Generation teams to support campaign landing pages and website experiences. * Collaborate with Product Marketing and Content teams to ensure messaging is clear, compelling and aligned to target audiences. * Partner with design and development teams to implement website improvements and new pages. * Track and report on website performance including conversion rates and pipeline contribution. * Continuously test and optimise website experiences to improve performance over time. **REQUIRED SKILLS/EXPERIENCE:** * 4\+ years of experience managing or optimising B2B SaaS websites. * Experience running conversion optimisation or experimentation programmes. * Strong understanding of website user journeys and landing page optimisation. * Experience working with marketing teams to support campaigns through website and landing page development. * Familiarity with tools such as HubSpot CMS, Google Analytics, Google Tag Manager and testing tools. * Strong analytical skills and ability to translate data into actionable insights. * Strong organisational skills with the ability to manage multiple projects simultaneously. * Comfortable operating in a fast\-paced, high\-growth environment.    WHY COGNISM At Cognism, we’re not just building a company \- we’re building an inclusive community of brilliant, diverse people who  **support, challenge, and inspire each other every day** . If you’re looking for a place where your work truly  **makes an impact** , you’re in the right spot! Our values aren’t just words on a page—they guide how we work, how we treat each other, and how we grow together. They shape our culture, drive our success, and ensure that everyone feels valued, heard, and empowered to do their best work. Here’s what we stand for: 🤝 **We Own the Outcome Together.** 🤓  **We Deeply Understand our Customers.** 🏆  **We Celebrate Impact Wherever It Comes From.** At Cognism, we are committed to fostering an inclusive, diverse, and supportive workplace. We welcome applications from individuals typically underrepresented in tech, so if this role excites you but you’re unsure if you meet every requirement, we encourage you to apply!

Healthtech & Digital Health
Precision AQ - International logo

Principal Medical Writer, Learning and Development

Precision AQ - International

Location not specified

**Principal Medical Writer – Learning \& Development** **📍** **Remote (UK\-based) \|** Occasional meet\-ups in London or Salisbury, plus client meetings as required **🏢** **Precision AQ \|** Award\-winning global healthcare communications agency We’re looking for a **Principal Medical Writer** to join our experienced **Learning and Development team** creating scientific training materials for healthcare professionals and pharma teams. If you are passionate about making complex science clear, engaging and interactive, we’d love to hear from you! **What You’ll Do** * Review content written by other writers in the team \- providing guidance, supporting with feedback, and taking responsibility for decision\-making * Lead client discussions * Provide strategic input into proposals and ongoing projects * Craft engaging, accurate and clear content: eLearning, workshops, infographics, videos, and more * Line manage/mentor writers in the team * Reference meticulously and collaborate on quality checks **What You Bring** * 6–8 years’ experience in a medical communications agency * Strong writing skills and scientific background * Confident reviewing content from other writers * Detail\-oriented and passionate about learning theory * Experience with training materials * Line management experience **What You’ll Get** * Collaboration with supportive, experienced teammates * Trust and independence to work remotely * Personalised feedback and development

Medical Education
AbbVie logo

Senior Manager, Regulatory Affairs

AbbVie

Maidenhead, England, UK

**Company Description** AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience \- and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.co.uk. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. **Job Description** * Located in Maidenhead (3 days per week Tuesday, Wednesday, Thursday) * Aligned with Neuroscience business unit * Excellent benefits and opportunities to progress **Job Overview** * Acts as the primary Regulatory contact for identified therapeutic area of responsibility. * Provides line management responsibility for a small team within UK Regulatory Affairs, including recruitment, goal setting, performance appraisal and talent development. * Oversees all regulatory activities within therapeutic area of responsibility, including maintaining licensing whilst contributing to the Brand Team priorities. * Uses experience and knowledge of the regulatory landscape to guide team to develop robust regulatory strategies and timely submissions to the Medicines and Healthcare Products Agency (MHRA), ensuring the fastest approvals, implementations and product launches. * Develops and maintains relationships with Area \& Affiliate members of GRS Europe and cross functional partners share knowledge, increase regulatory awareness and build networks. * Engages externally with the Health Authority on regulatory submissions and/or other pharmaceutical industry trade associations, as required. * Supports the business in planning for and execution of product launches, acquisitions and divestitures, as required. **Key Accountabilities** **Regulatory Strategy and Tactical Implementation** * Provides clear guidance and recommendations on UK regulatory strategies and tactical plans throughout a product lifecycle including clinical trial submissions, management of variations, paediatric investigation plans, new marketing authorisation applications and liaison with local regulatory authorities. * Reviews regulatory submissions for UKRA team for assigned areas of responsibility, corrects where necessary and provides feedback. * Regulatory intelligence and external landscape monitoring, + Interacts with Regulatory policy makers and professional associations (eg ABPI) to gather knowledge about trends, future changes and current landscape in accordance with the national and EU legislation and relevant Associations’ Codes and advocate for AbbVie’s interests. **Regulatory Compliance** * Ensures compliance with AbbVie’s policies and procedures to meet statutory, quality and business requirements, acting as primary point of regulatory contact for audits and inspections in the UK as appropriate and supporting oversight of divisional policies and procedures. * Ensures compliance with UK legislation for Medicines, Medical Devices, clinical trials and paediatric investigation plans and has an awareness of the ABPI code. **Liaison with Internal Stakeholders** * Acts as Regulatory liaison with Area and local UK cross functional teams to ensure UK strategies align with global strategies, whilst maintaining compliance with local regulations. + Understand and articulate the regulatory perspective across the business, translating key regulatory decisions in terms of impact on products in the UK. * Acts as lead Regulatory representative on Affiliate committees/initiatives (as required). * Acts as deputy to the UK Regulatory Affairs Managers and/or Director (as required). **Leadership for UK Regulatory Therapeutic team** * Provides strong leadership and direction to the UK Regulatory Therapeutic Regulatory team to support: + Successful implementation of regulatory product strategies + Develops and maintains strong working relationships with MHRA and local pharmaceutical company trade associations + Process improvements, internal compliance and team consistency + Individual professional development, improved capability and upskilling within team + Supports recruitment activities (as required) and retain high calibre regulatory affairs professionals **Qualifications** * Experienced Regulatory professional in the pharmaceutical industry with a clear understanding of the UK regulatory and submissions process * Experience as a line manager with highly developed people skills * Sense of personal responsibility and accountability, with a positive, can\-do attitude * Ability to multitask, prioritise, and manage multiple projects and deadlines * Ability to work effectively and collaboratively across cultures and cross\-functionally * Strong diplomacy, influencing, presentation skills **Personal Skills** * Consultative and collaborative interpersonal style * Excellent written, verbal and interpersonal skills (in English) * Ability to identify compliance risks and escalate when necessary * Life Sciences Degree in relevant subject area * Computer literate Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. US \& Puerto Rico only \- to learn more, visit https://www.abbvie.com/join\-us/equal\-employment\-opportunity\-employer.html US \& Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join\-us/reasonable\-accommodations.html

Pharma & Biotech
UCB logo

Non-Clinical Safety Lead - UK

UCB

Slough, England, UK

**Make your mark for patients** To strengthen our **Non\-Clinical Safety Evaluation** group within **Early Clinical Development and Translational Science** , we are looking for a talented individual for the role of **Non\-Clinical Safety Lead** , based in **Braine L'alleud, Belgium or Slough, UK or Cambridge, MA (USA).** **About The Role** As a Non\-clinical Safety Lead, you will provide scientific leadership for non\-clinical safety across discovery and development programs. You will shape non\-clinical strategies, ensure high\-quality execution, and support regulatory interactions from early development through clinical progression and post approval. You will: * Lead, communicate, and execute non\-clinical safety strategies aligned with clinical development goals. * Develop integrated non\-clinical safety plans supporting innovative programs. Ensure timely delivery of high\-quality non\-clinical data and global regulatory documentation. * Represent UCB in interactions with regulatory authorities and external partners. This role is well suited to an experienced toxicologist—ideally with exposure to gene and cell therapy or other novel modalities—who enjoys working at the interface of science, development strategy, and regulation. You will thrive in an environment where you can share expertise across functions and global UCB sites, engage with cutting\-edge science and build collaborative networks to drive cross\-functional success. **What You'll Do** * Provide non\-clinical safety expertise to discovery and development projects * Define, lead, and implement non\-clinical safety strategies across programs. * Partner with clinical teams to ensure robust preclinical data supports clinical trial design. * Contribute to global regulatory submissions (e.g., IBs, Briefing Books, INDs, NDA/BLAs) and interact with regulatory authorities. * Oversee the design, review, and interpretation of non\-clinical studies. * Manage non\-clinical safety programs, including budgets. **Interested? For this role you’ll need the following education, experience and skills** * PhD in Toxicology, Pharmacology, or related discipline (or equivalent MS/DVM with experience). * 5\+ years in non\-clinical safety (preferably in pharma or biotech). * Deep understanding of regulatory processes and regulatory toxicology. * Experience managing and forecasting non\-clinical safety budgets. * Ability to produce high\-quality reports and submission documents with subject matter expert support. **Preferred Qualifications:** * Accredited or registered toxicologist. * Experience in gene and cell therapy and/or other novel modalities. Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you! **About Us** UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9\.000 people in all four corners of the globe, inspired by patients and driven by science. **Why work with us?** At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential. At UCB, we’ve embraced a hybrid\-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office. UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA\-Reasonable\_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Public Health, Policy & Government
BioMarin Pharmaceutical Inc. logo

Executive Director, International Pricing, Access, Value, and Evidence (Flexible Location)

BioMarin Pharmaceutical Inc.

London, England, UK

Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well\-understood biology and provide an opportunity to be first\-to\-market or offer a substantial benefit over existing therapeutic options. **Summary Description** The Executive Director, International Value \& Access, will report to the SVP, Head of Pricing, Access, Value and Evidence (PAVE) and will be a member of PAVE leadership team. The position and his/her team will be responsible for the strategic planning, design and local implementation of access and pricing strategies to support the launch, pricing and reimbursement of BioMarin's products in markets outside of the US in Europe, MEA, LaTam and APAC. This position has a flexible location in Europe, LatAm or East US **Responsibilities** * Execute strategies and plans addressing health care payer\-related barriers to product access * Monitor the regional reimbursement environment by tracking government policy initiatives and associated commercial implications, and profiling reimbursement environment for marketed and pipeline products * Utilize key market research, advisory board, and other patient/ field inputs to continually monitor market trends and dynamics and assess their business implications * Monitor relevant country\-specific policy initiatives and associated commercial implications, and profile the environment for marketed and pipeline products * Collaborate with Country Managers and Area Directors to analyze the commercial implications of new or pending reimbursement policy and/or legislative proposals potentially impacting reimbursement for BioMarin products * Participate on brand, government contracts/pricing, and other commercial teams * Collaborate closely with Global PAVE teams (HEOR, Pricing, V\&A) other commercial groups including Field Sales, Market Planning, Marketing, and Commercial Operations across the region * Collaborate closely with other corporate groups also monitoring the legislative and regulatory environment (e.g. Government Affairs, Regulatory Affairs, and Medical Affairs) * Assist Country Managers and Areas Directors in the preparation and submission of reimbursement dossiers. * Monitor development of government programs for reimbursement of orphan drugs/rare diseases SCOPE International scope including Europe, LatAm, MEA and APAC EDUCATION * BS/BA degree in Business or Life Sciences * Fluent English. **Experience** * Minimum 15\+ years of commercial experience in the pharmaceutical industry, with minimum of 10\+ years management experience in Market Access. * Experience leading multicultural teams. * With experience of specialty care products in highly competitive markets. Experience in rare diseases market would be a plus * Proven track record of marketing across multiple stages of a products life cycle * Successful Global launch experience in specialty and/or rare disease, preferably in the specific therapeutic area. * Strong leadership skills and business acumen * Deep strategic marketing expertise (launch, branding, analytical skills, targeting, segmentation, life cycle management in particular) * Demonstrated agility, accountability, sense of urgency and team spirit * Capability to embark and enroll cross functional stakeholders at all levels of the organizations * Ability to build strong relationships across cultures, backgrounds and functions * Can manage complex situations and demonstrated ability to make decisions * Strong planning and project management skills – can and has successfully driven projects involving several departments and functions * Ability to convey complex information succinctly \& simply (including verbal, written and in presentations) * Resilience and openness to change * Complies with Company guidelines and country/industry standards on ethics and compliance and acts as a role model for ethical behavior Note: This description is not intended to be all\-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned. Equal Opportunity Employer/Veterans/Disabled An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Medical Device
Bruker logo

Territory Account Manager, MDx UK North (m/f/d)

Bruker

Greater London, England, UK

**Overview** Bruker is enabling scientists and engineers to make breakthrough post\-genomic discoveries and develop new applications that improve the quality of human life. Bruker’s high performance scientific instruments and high value analytical and diagnostic solutions enable scientists to explore life and materials at molecular, cellular, and microscopic levels. In close cooperation with our customers, Bruker is enabling innovation, improved productivity, and customer success in post\-genomic life science molecular and cell biology research, in applied and biopharma applications, in microscopy and nanoanalysis, as well as in industrial and cleantech research, and next\-gen semiconductor metrology in support of AI. Bruker offers differentiated, high\-value life science and diagnostics systems and solutions in preclinical imaging, clinical phenomics research, proteomics and multiomics, spatial and single\-cell biology, functional structural and condensate biology, as well as in clinical microbiology and molecular diagnostics. For more information, please visit  www.bruker.com . Bruker Molecular Diagnostics is at the forefront of transforming how infectious diseases are detected and managed, combining innovative molecular technologies with streamlined, sample\-to\-result workflows. Guided by a commitment to innovation with integrity, the team works closely with NHS and clinical laboratories to deliver solutions that improve diagnostic speed, accuracy, and efficiency. It’s an environment that blends commercial drive with scientific credibility \- where individuals have the opportunity to shape laboratory practice, support critical patient pathways, and contribute meaningfully to the evolution of molecular diagnostics. We are seeking a **Territory Account Manager (TAM)** to drive growth across North, East Midlands England and Scotland. This field\-based role involves building strong relationships with NHS and clinical laboratory customers, developing new b usiness opportunities, and managing a structured pipeline to deliver against commercial targets across the region. **Responsibilities** * Financial goals: * Deliver annual sales targets and manage territory forecast * Maintain accurate pipeline and contribute to forecasting processes * Territory management : * Develop and execute a structured territory plan focused on new opportunity creation and account growth * Maintain clear visibility of account status, pipeline progression and next steps * Account management: * Build and maintain strong relationships with laboratory stakeholders, clinicians, procurement teams, Managed Service Contract (MSC) providers and operational leads * Work cross\-functionally (Applications, Service, Customer Support) to ensure customer satisfaction and retention * Maintain detailed account knowledge including revenue trends, contractual status, competition and customer buying intentions, ensuring proactive identification of opportunities and risks * Opportunity management: * Identify, qualify and actively progress opportunities towards decision and close * Drive consistent movement from initial engagement through active sales stages to contract award * Generate and develop opportunities through direct marketing, conference participation, exhibitions, events and customer visits * Expand presence into new accounts, building a sustainable pipeline * Maintain a structured and regularly updated pipeline with clearly qualified opportunities, realistic timelines and defined next steps * Value proposition: * Understand and demonstrate the unique value proposition of Bruker MDx solutions, aligning capabilities to specific customer needs, clinical workflows and operational priorities * Present, promote and demonstrate the value of the MDx portfolio to laboratory and clinical stakeholders * Deliver seminars, presentations and product evaluations aligned to customer needs * Tender, framework and proposal management: * Coordinate and deliver the preparation and submission of tenders and proposals in line with NHS requirements and deadlines * Ensure submissions are timely, accurate and compliant * Negotiation and close: * Negotiate contracts and agreements to achieve favourable outcomes * Drive closure of opportunities in line with agreed timelines * Reporting: * Deliver consistent forecast accuracy * Maintain high\-quality sales reporting including opportunity stages, values and timelines * Execution: * Execute tasks and customer follow\-up within agreed timelines, with proactive escalation of risks or delays * Market intelligence \& feedback: * Monitor competitor activity and market dynamics * Provide structured feedback to internal stakeholders to support strategy and product development This role has responsibilities for the full Bruker MDx portfolio \- Hain Lifescience and ELITech MDx products and will therefore require an understanding of and alignment with the processes of each entit **Qualifications** * BSc (or equivalent) in Biomedical Sciences, Life Sciences, or a related discipline; postgraduate experience in diagnostics or healthcare is desirable * Demonstrated experience in a commercial or customer\-facing role with responsibility for delivering against defined targets * Proven sales or account management experience, including managing opportunities and progressing deals through a structured sales cycle * Experience building and maintaining a robust pipeline and delivering sustained revenue growth * Strong experience developing and growing customer relationships within complex, multi\-stakeholder environments * Experience operating within NHS or comparable public sector healthcare environments, including procurement p rocesses and tender\-based purchasing, is highly advantageous * Experience in diagnostics, life sciences, or healthcare is essential; molecular diagnostics and/or sequencing experience is strongly desirable * Experience contributing to or leading tender submissions within structured procurement frameworks * Familiarity with recurring revenue or consumables\-based business models is advantageous * Good awareness of competitive products, positioning, and market dynamics * Strong personal drive, accountability, and results\-oriented mindset, with a track record of delivery * High standards of work, with a structured, disciplined, and consistent approach to execution * Ability to manage multiple priorities in a fast\-paced commercial environment * Strong organisational and communication skills, with the ability to build effective internal and external relationships * Collaborative and team\-oriented mindset * High level of integrity, professionalism, and commitment to corporate compliance * Experience using CRM systems (e.g. Salesforce) for pipeline management, activity tracking, and reporting * Strong written and verbal communication skills in English

Healthtech & Digital Health
Practice Plus Group logo

Patient Engagement Lead

Practice Plus Group

Staffordshire, England, UK

**About The Role** **UNLOCK YOUR BEST WORK LIFE** **\+ MAKE A DIFFERENCE TO EVERY LIFE** We have an exciting opportunity for a Patient Engagement Lead to join team at HMP YOI Swinfen Hall a Category C men's prison and Young Offenders Institution, located in the village of Swinfen in Staffordshire, England. We are looking for someone to support and enhance our health promotion with young adults! **Hours** The site currently offers Monday \- Friday: core office hours **Salary** This position is full time, you’ll receive an annual salary from £29,264 to £33,510 per annum \- depending on experience. **How will we support you?** * * Bespoke induction, including our Introducing Health in Justice training course * * Competency framework * * Regional and national career development opportunities * * Our bespoke Learning Management System to address your learning needs * * Support from the wider team **Candidates are required to have a Legal right to work in the UK and due to the nature of the role, offers of employment will be subject to additional vetting and security checks** What you'll be doing As our new Patient Engagement Lead your responsibilities will vary. You will: * Responsible for the improvement and stability of patient engagement activities and patient satisfaction through effective service user engagement and peer led forums, the planning and delivery of projects/programmes in line with patients’ needs and priorities, involving patients (where possible) in project and training delivery. * You’ll act as a point of contact and respond to patient engagement enquires from staff, external partners and patients. * Additionally, within this role, you will be responsible for the oversight and management of the health champion peer support model, including the delivery of Health Champion training across the site. If you are interested in **career development,** we have a wide range of opportunities for you to develop your skills and experience, which include both **internal and external options** for development and learning. **It doesn’t stop there** … we also offer: * Discounts on shopping and leisure activities * Support to grow in your role and continue your professional development * 24/7 employee assistance helpline and financial assistance when you need it What we'll look for in you The Health in Justice team at Practice Plus Group makes a real difference across over 53 prisons, young offenders and immigration removal centres. We’re the UK’s leading independent provider of NHS services to over 40,000 patients in secure environments, always putting their needs first, regardless of their background. Practice Plus Group’s purpose is to Unlock your best work life and we stand by our core values: * we treat patients and each other as we would like to be treated * we act with integrity * we embrace diversity * we strive to do things better together We are looking for caring, compassionate but also driven professionals who can help us drive our vision for a fair and inclusive healthcare access to all. **Qualifications, skills and experience required:** * Provide outstanding patient experience by seeking out, listening to and acting on their feedback, so that care is personalised and informed by what matters to them. You will work closely with patients, healthcare and prison colleagues to ensure the patient is at the centre of service delivery. * Deliver a fully embedded process for patient engagement to manage compliments and complaints, to ensure patients’ needs are met. * Expereince supporting patients in a healthcare setting \- desired Secure environments are one of the most challenging, yet rewarding places for healthcare professionals to work. If you’re looking for a role where you can develop your existing healthcare skills and learn something new every day in an environment that never stands still, then this could be the right opportunity for you.

Pharma & Biotech
Rentokil Initial Careers logo

Graduate Regulatory Officer

Rentokil Initial Careers

Crawley, England, UK

**Job Purpose** Join the Technical Services Regulatory Team within Rentokil Initial's Marketing and Innovation (M\&I) Function. In this role, you will support technical and commercial compliance for chemical products and services across Rentokil Initial's global business activities. Your primary focus will be to maintain chemical regulatory compliance, execute swift corrective actions when non\-compliance is identified, ensure accurate product safety and labelling, and support product registration and launch workflows across international markets. **Key Responsibilities \& Accountabilities** * Regulatory Risk \& Compliance Management: Assist in protecting Rentokil Initial from commercial and technical risks associated with national and international chemical regulations and directives * Corrective Action Execution: Help implement urgent corrective actions across Rentokil Initial businesses to mitigate identified regulatory risk exposures promptly * Technical \& Documentation Support: Draft and review Safety Data Sheets (SDS), product classifications, product labels, and packaging specifications in compliance with global standards * Product Registration \& Market Entry: Support the end\-to\-end process of obtaining, updating, and maintaining chemical product registrations to enable smooth market introduction of new products * Database \& Systems Management: Maintain accurate, up\-to\-date product safety records and compliance data within company regulatory systems and software (e.g., LISAM) **Requirements** **Required Skills \& Qualifications** * Education: Bachelor's degree (BSc) or higher in Chemistry, Toxicology, Environmental Science, or a related scientific discipline * Regulatory Knowledge: Foundational understanding of global chemical regulatory frameworks covering registration, hazard classification, chemical safety, transport (ADR/IMDG/IATA), and waste disposal * Technical Systems: Proficiency with chemical regulatory software and databases (experience with LISAM SDS software is highly desirable) * Data Analysis \& Quality Focus: Strong analytical skills, meticulous attention to detail, and a structured, process\-driven approach to complex problem\-solving * Proficiency in additional European languages is a strong advantage **Key Personal Attributes** * Collaborative \& Ethical: A team\-oriented professional with sound judgment, high integrity, and commitment to corporate ethics * Communication \& Stakeholder Management: Excellent interpersonal skills with the ability to communicate effectively with cross\-functional global teams, suppliers, and internal stakeholders * Problem\-Solving Mindset: Creative and diplomatic approach to overcoming technical, supply chain, and compliance challenges without compromising safety standards * Customer\-Centric \& Organized: Service\-focused ethic with disciplined time management to consistently meet tight regulatory deadlines **Benefits** * Competitive salary * Hybrid working * Rentokil Initial Reward Scheme * 23 days holiday, plus 8 bank holidays * Employee Assistance Programme * Death in service benefit * Healthcare * Free parking At Rentokil Initial, our customers and colleagues represent diverse backgrounds and experiences. We take pride in being an equal opportunity employer, actively encouraging applications from individuals from all walks of life. Our belief is that everyone irrespective of age, gender, gender identity, gender expression, ethnicity, sexual orientation, disabilities, religion, or beliefs, has the potential to thrive and contribute. We embrace the differences that make each of our colleagues unique, fostering an inclusive environment where everyone can be their authentic selves and feel a sense of belonging. To ensure that your journey with us is accessible if you have any individual requirements we invite you to communicate any specific needs or preferences you may have during any stage of the recruitment process. Our team is available to support you; feel free to reach out to (joanna.sharpe@rentokil\-initial.com) if you need anything Be Yourself in Your Application! At Rentokil Initial, we value innovation, but we want to see the real you! While AI can help with structure and grammar, make sure your application shows your true passion and understanding of the role. A personal touch will help you stand out.

Pharma & Biotech
Health Partners Group logo

Client Implementation Manager (Homebased)

Health Partners Group

Location not specified

At Health Partners, we pride ourselves on being one of the UK’s leading providers of occupational health and wellbeing solutions. We partner with organisations across diverse industries, helping them to support the physical and mental health of their employees. *Please note that the closing date for this vacancy is subject to change and the advert may close earlier if sufficient applications are received. We encourage early applications to avoid disappointment.* **JOB REF: JOB7216** **Role Outline** The Client Implementation Manager is responsible for leading and coordinating the end‑to‑end onboarding and implementation of new clients and services. This role ensures that solutions are delivered on time, within scope, and aligned with client expectations. The ideal candidate combines strong project management skills, excellent communication, and a client‑focused mindset to drive successful adoption and satisfaction. **What You Will Be Doing** * Lead the full client implementation lifecycle from kick‑off to go‑live. * Develop detailed project plans, schedules, and milestones, ensuring alignment with internal teams and client stakeholders. * Facilitate requirements gathering and ensure solution configuration meets client needs. * Identify project risks and issues, providing proactive solutions to ensure project success. * Serve as the primary point of contact during implementation, providing regular updates and ensuring expectations are managed effectively. * Build and maintain strong, trusted relationships with client stakeholders at all levels. * Provide guidance and training to clients on product functionality, processes, and best practices. * Partner with product, engineering, operations, and support teams to ensure seamless delivery. * Escalate issues appropriately and drive resolution across internal teams. * Provide feedback to internal teams on client requirements, product enhancements, and process improvements. * Track project progress, risks, deliverables, and resource allocation. * Produce and deliver regular status reports, implementation summaries, and KPIs to both clients and leadership. * Ensure all documentation is complete, accurate, and accessible for internal and client use. **What We Are Looking For** We are seeking a highly motivated and experienced professional with a strong background in Project Management, IT, or a related field. The ideal candidate will have 3 to 5 years of proven experience in client implementation, project management, or client delivery roles, showcasing a track record of successfully managing complex, multi\-stakeholder client onboarding initiatives. Proficiency in project management tools, such as MS Project, is essential, along with exceptional analytical, organisational, and problem\-solving skills. Excellent verbal and written communication abilities are critical to effectively collaborate with diverse teams and stakeholders. While not required, candidates holding a Project Management certification and demonstrating technical aptitude, particularly in translating business needs into technical requirements, will be highly regarded. We are looking for someone who thrives in a dynamic environment and is eager to deliver exceptional results. **Hours** The role is full\-time and will involve working 37\.5 hours per week, Monday to Friday between the hours of 8am and 6pm. **Location:** This role is homebased, occasional onsite visits may be required for the role. **Salary** The salary for this role is up to £45,000K depending on experience and qualifications. **Company Benefits** We value the people who work with us and our rewards package is reviewed regularly to reflect this. * Competitive annual salary dependent on qualifications and experience * Contributory pension scheme up to 6% * Life assurance * Starting on 25 days annual leave plus bank holidays, increasing with length of service * Have a day off for your Birthday (non\-contractual benefit) * Discounted gym membership * Health cashback plan **About Health Partners** Health Partners are committed to transforming the way health and wellbeing services are delivered in the UK. As one of the UK’s leading providers of occupational health and wellbeing solutions, we work with organisations across a wide range of industries to support the physical and mental health of their employees. Our mission is simple: to empower people to lead healthier, happier, and more productive lives. With a strong focus on innovation and excellence, Health Partners combines clinical expertise with a personal, compassionate approach. Our multidisciplinary team of healthcare professionals, including occupational health advisors, physicians, physiotherapists, and counsellors, delivers tailored, evidence\-based solutions designed to meet the unique needs of our clients and their workforce. We pride ourselves on fostering long\-term partnerships built on trust, professionalism, and results. Whether it’s through workplace health assessments, proactive wellbeing initiatives, or mental health support, Health Partners is dedicated to making a real difference. At the heart of Health Partners is a culture of collaboration and continuous improvement. We believe in investing in our people and providing opportunities for growth, ensuring that our employees feel valued and inspired to deliver their best. By joining Health Partners, you’ll become part of a dynamic team that’s passionate about driving positive change in the workplace and beyond. If you’re ready to make a meaningful impact in the field of health and wellbeing, we’d love to hear from you. Together, we can build healthier futures. **Diversity \& Inclusion Statement** *Health Partners are a proud member of the Disability Confident employer scheme* Health Partners are extremely proud to support the needs of our employees and as such understands everyone has individual work and home life responsibilities. We’re happy to discuss flexible working arrangements for this role, should this be a requirement for you. We aim to become one of the most inspiring companies to work for and to achieve this ambition, we need the best talent to come and work for us. We look for candidates with the right skills and values to join us and selection is based on a fair and equal process. We’re proud to be committed to equal opportunities and welcome applications from all backgrounds. Diversity and Inclusion forms an integral part of everything that we do, bringing together the best talent, helping people to realise their full potential by being yourself at work and delivering an outstanding service to everyone – regardless of difference.

Healthtech & Digital Health
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