Regulatory Affairs Associate

Regulatory Affairs Associate

Office-based (with some flexibility)

Occasional national & international travel

Salary: £42,000 -£44,000

Location; Gloucester

We are looking for a detail-driven and motivated Regulatory Affairs Associate to join a growing and dynamic team within the medical devices sector.

This is a fantastic opportunity to play a key role in ensuring regulatory compliance across international markets, supporting the development of life-changing products while working in a highly collaborative, quality-focused environment.

What You'll Do

Support MDR technical documentation (Annex II & III)
Contribute to UK & international registrations (MHRA, EU, FDA)
Maintain ISO 13485 compliant documentation
Assist with PMS, vigilance, and audits
Collaborate across Engineering, Quality & Manufacturing
Review labelling and compliance for global markets
What You'll Bring

2+ years in medical device regulatory or quality
Strong knowledge of MDR, MDD & ISO 13485
Excellent attention to detail & technical writing
A proactive, organised and team-focused mindset
How to Apply

If you're an experienced looking to make a significant impact within a forward-thinking medical device manufacturer, apply today through Hawk 3 Talent Solutions.

If you would like to apply for the role ofRegulatory Affairs Associate, then please email your CV to (url removed) or call Donna on (phone number removed).

Closing date is 27.06.2026. Please note this could change subject to suitable applications.

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Hawk 3 Talent Solutions are committed to the selection, recruitment and development of the best people, basing judgements solely on suitability for the job. Whilst we endeavour to respond to all applications individually, due to high volumes, this is not always possible. Thank you for your interest in this role and we look forward to working with you in the future
Only candidates based in UK and eligible to work in UK are allowed