Validation Engineer

Key Skills - Validation Engineer, ISO 13485, FDA, GMP, IQ, OQ, PQ, Medical Device

A world leading manufacturer of medical device components requires a validation engineer on an initial 6-12 month contract due to increased project work.

This role requires a validation engineer to propose, gain approval, document and implement process Validation procedures to ISO13485 and FDA regulations.

You'll demonstrate experience of generating and implementing IQ, OQ and PQ protocols
combined with the ability to generate GAP analysis of processes and equipment validation status relating to the business. An understanding of ISO 13485 and previous experience in the pharmaceutical or medical device industry is vital for this position.

This validation engineer position will give you the opportunity to work on an extensive new project and also has the potential of leading to a long term contract.

To apply: Please forward your most up to date CV or call me in confidence.

Key Skills - Validation Engineer, ISO 13485, FDA, GMP, IQ, OQ, PQ, Medical Device

JAM Recruitment is acting as an employment business with regards to this position.