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Senior Quality Engineer (Integration Programme)

EPM Scientific

Belfast, Northern Ireland, UK
Contract
Medical Device
Posted 28 Aug 2026

Job Description

Senior Quality Engineer (Integration Programme)

Location : Belfast, Northern Ireland (On-Site)

Contract Length : Up to 24 Months

Hours : Full-time (40 hours per week)

Start Date: ASAP

Responsibilities

  • Assess the acquired site's quality system, engineering processes and manufacturing controls against standards and identify integration requirements.
  • Perform gap assessments across procedures, validation activities, risk management processes, FMEAs and quality documentation.
  • Develop and execute plans to harmonise local processes with Quality Management System.
  • Support the integration and remediation of FMEAs, risk files, process documentation and manufacturing quality records.
  • Execute process validation activities where required, including validation remediation and implementation of appropriate controls.
  • Review production and process controls, working with manufacturing teams to ensure compliance and alignment with corporate requirements.
  • Support first article inspections, process improvements and quality engineering activities across the site.
  • Drive quality system improvements, corrective actions and integration workstreams throughout the acquisition programme.
  • Work closely with cross-functional Quality, Engineering and Manufacturing stakeholders to deliver integration milestones.
  • Operate as a hands-on project resource, supporting both strategic integration activities and day-to-day execution on the manufacturing floor.

Requirements

  • 5-15 years' experience in medical devices or another highly regulated manufacturing environment.
  • Strong background in Quality Engineering, Validation and risk management activities, including FMEAs and process controls.
  • Hands-on experience executing process validations (IQ/OQ/PQ) and supporting remediation or integration projects.
  • Engineering-led profile with exposure to QMS, CAPA, non-conformances and quality system improvements.
  • Comfortable working autonomously on-site and collaborating with manufacturing, quality and engineering stakeholders.
  • Previous experience within acquisitions, site integrations, quality transformations or manufacturing improvement programmes would be advantageous.

Interested in this role?

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