Senior Regulatory Affairs Officer

SRG
Edinburgh, United Kingdom
9 months ago
Applications closed

Related Jobs

View all jobs

Senior Regulatory Affairs Specialist UK and Ireland

GI Group Tottenham Court Road, London, United Kingdom

Senior Quality Assurance and Regulatory Affairs Engineer

HAYS Specialist Recruitment Swindon, United Kingdom

Senior Director Medical Affairs, Oncology Precision Diagnostics

QIAGEN Manchester, United Kingdom

Senior Manager/Associate Director Clinical Data Transparency, EHDS Data Cataloguing

Johnson & Johnson MedTech High Wycombe, United Kingdom

Senior Manager / Associate Director, Clinical Data Transparency, EHDS Data Cataloguing

Johnson & Johnson MedTech Belgium

Senior Manager / Associate Director, Clinical Data Transparency, EHDS Data Cataloguing

Johnson & Johnson MedTech
Posted
20 Jan 2026 (9 months ago)

Senior Regulatory Affairs (RA) Officer - Edinburgh - Medical Devices

SRG are delighted to be working with an internationally renowned medical device manufacturer. As part of continued growth this organisation are looking for a Senior Regulatory Affairs (RA) Officer to join their team in the greater Edinburgh area.

The Role

As Senior RA Officer you will work as part of a large, multinational team to help manage and deliver product licence registration, working in collaboration with regulatory bodies across the globe.

As a key part of the RA team you will help build the company's regulatory strategy, determine requirements and propose solutions to ensure compliance. On a day-to-day basis this involves the preparation of regulatory documentation and subsequent submission across the US, UK and EU as well as other appropriate territories in line with local guidance.

You will be required to work closely with internal and external stakeholders to ensure all staff and vendors are kept aware of developments and changes in global regulatory requirements. As Senior RA officer you will also be responsible for managing and confirming compliance issues both internally and externally, ensuring all relevant documentation is kept accurate and up-to-date.

The Right Person

Prior experience in a regulatory role - ideally within an FDA licensed manufacturing facility.
Significant previous experience within the medical device sector is essential, anyone with prior experience working with IVDs would be preferential.
Excellent communication skills are essential
Expert-level knowledge of CE and FDA regulations, including PMA, BLA, and 510(k) submissions.
Demonstrable experience supporting regulatory audits and inspections

What's in it for you?

This position offers a competitive base salary with a wide array of benefits available. As well as this you will be offered a variety of opportunities for personal development working within a large multi-national team.

Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.