Experienced Regulatory and Compliance professional
£45k - £55k
Responsible for managing ISO 13485, DAMAS, MHRA, and ISO 27001 compliance frameworks within medical device manufacturing environment
- Skilled in quality systems, audits, risk management,
- Awareness of post-market surveillance, cybersecurity compliance, and intellectual property management
- Experienced in embedding regulatory standards into business operations while supporting continuous improvement, product quality, and customer confidence.
Key skills required
- Ability to interpret and implement regulatory standards
- Understanding of ISO 27001 principles
- Managing patent, trademark, and licencing documentation working with legal teams
Equivalent experience
- Regulatory Affairs
- Quality Management
- Medical Engineering
- Biomedical Science
- Healthcare Technology
- Engineering or Manufacturing
If you are interested in this role call Katie on or email
Skills:
Patents cybersecurity compliance audits
INDPRO
Pay: £45,000.00-£55,000.00 per year
Benefits:
- Company pension
- On-site parking
Application question(s):
- Must be confident in MHRA Guidelines and ISO 13485
Work authorisation:
- United Kingdom (required)
Location:
- Enniskillen, County Fermanagh (preferred)
Work Location: In person
