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Quality Assurance/Regulatory Affairs/Medical Device/South West

Eingestellt von Sentinel IT LLP

Gesuchte Skills: Engineering, Design

Projektbeschreibung

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.

Projektdetails

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Sentinel IT LLP

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