https://jobs.co.uk/job/regulatory-affairs-specialist-srg--bff7de5b-b5d1-4502-b3b5-55dca14fa836 RSS feed for Regulatory Affairs Specialist at SRG. en-gb Wed, 24 Jun 2026 09:22:45 GMT https://jobs.co.uk/job/regulatory-affairs-specialist-srg--bff7de5b-b5d1-4502-b3b5-55dca14fa836 https://jobs.co.uk/job/regulatory-affairs-specialist-srg--bff7de5b-b5d1-4502-b3b5-55dca14fa836 Sun, 21 Jun 2026 23:00:00 GMT Location: Perivale | Salary: £50000 - £60000/annum | Type: Permanent | About the Role We are seeking an experienced Senior Regulatory Affairs Specialist to join a SME Medical Device company. This is a key role responsible for ensuring our medical devices meet global regulatory requirements and maintain compliance across all markets.You''ll play a pivotal role in supporting product registrations, maintaining technical documentation, and working closely with cross-functional teams to ensure regulatory excellence throughout the product lifecycle. What You''ll Be Doing As a Senior Regulatory Affairs Specialist, you will: Regulatory Submissions & Compliance Prepare and submit regulatory documentation and product registration dossiers Maintain regulatory approvals, licences, and certificates across the portfolio Coordinate renewals to ensure continuous market access Technical Documentation & Clinical Evaluation Develop and maintain Technical Documentation in line with EU MDR (2017/745) and ISO 13485 Support clinical evaluation activities, including plans, reports, and post-market clinical follow-up Ensure labelling and marketing materials comply with regulatory standards Contribute regulatory expertise during product design and developme... Permanent