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.