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 02890994111 or email Katie@blackfoxsolutions.co.uk
