Validation Specialist, Belgium

Overall this role will focus on ensuring proper execution of the validation strategy procedures and application of cGMP (URS, FMEA, Validation Master Plan, Installation Operational Qualification and Performance Qualification). This will include the review of User Requirements and establishment of a Validation Master plan, and managing and tracking each activity to ensure timely completion of the validation plan in coordination with Contractors/Suppliers, Engineering, Production, Quality Control, and Quality Assurance.

A desirable profile would be a degree qualified Pharmaceutical professional with good experience in managing qualification projects. Useful is experience from qualifying equipment such as Autoclaves, Aseptic manufacturing, Filling equipment, Capping equipment, or generally equipment used in
Vaccine manufacturing facilites.
Must be fluent in English and French.

For more information on this vacancy, or any other medical device opportunities, please contact the Senior Consultant Andrew Boroky on 0044 (0) 207 940 2116, or email him at a.boroky@nonstop-devices.

http://www.eurojobs.com/en/candidate/jobs/158937.html

Categoria: estrangeiro

Tags application • manufacturing • production quality control • qualification • Quality • URS • validation master plan • validation plan • validation specialist • validation strategy

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