Position title: VP of Regulatory Affairs

Reports to: CEO

Location: Crawley, West Sussex

Department: QA/RA

Employment Type: Full-Time (UK)

Minimum Experience: Senior Manager/Supervisor



Position summary

The VP of Regulatory Affairs is responsible for the quality and regulatory activities of the organization, including the Quality Management System (QMS) and products in accordance with international standards, best practice and customer requirements.


Relevant Knowledge and Skill requirements

Establish and maintain an effective Quality Management System (QMS) in accordance with all applicable medical device regulations, including ISO 13485, US FDA Quality Systems Regulation (QSR), and Medical Devices Single Audit Programme (MDSAP). Lead Continuous Improvement of the Quality Management System. Input to regulatory aspects of technology & product opportunity evalu...