Location
Crawley
Job Type
fulltime
Posted
July 15, 2026
Job Description
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...
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...