Description
Quality Assurance/Regulatory Affairs/Medical Device/South West England- ISO13485
My client, a highly reputable Medical Device company in Wiltshire, is looking for a Quality Assurance and Regulatory Affairs Specialist to work on a contract basis.
Key responsibilities include:
-ISO 13485 standard practices
-Maintaining Design History Files
-Participating in failure investigations
-Execute all duties in compliance with GMP
Education/Qualifications needed:
-Degree in Scientific/Engineering discipline (or relevant experience)
-Experience in Medical Device industry
-Qualified internal or lead auditor ISO 13485
-Proven track record in compiling Design History Files
Full details upon request. Please apply with your CV below.
Full details available upon request.
Please apply with your CV below.