Regulatory Specialist

BioTalent is currently partnered exclusively with an SME Class 2 Device business who are looking to find their latest addition to their regulatory team

The role with give you:

• A chance to work across both NPD and NPI
• Work in global markets
• Support by a senior leader that BioTalent has had many years of working with
• Variety of tasks

You will need to bring in:

• Minimum of 3 years of experience within regulatory affairs within Medical Devices or IVD
• Experienced working ISO 13485
• Hands on experience with technical file creation, MDR updates and some exposure to registrations
• Ideal candidates will have worked within global markets such as US or MDSAP countries

If this role sounds interesting please apply or reach out on michael.kakoullis@biotalent.com or call +447833626032