Process & Validation Engineer – REF 01978MQ

Headcount Solutions is seeking a Process and Validation Engineer for a long term global project on a 12 month rolling contract.

The project involves the development of a medical device which will be manufactured using a polymer synthesis process in the US with the finishing operations in Ireland.  The role requires interaction with both  teams in the US and Ireland.

The main responsibilities are:

•       Interactions with the US team to optimize and validate the polymer synthesis process.

•       Develop packaging solutions with the vendors for the final product.

•       Validation of the finishing process at the client site.

•       Developing client standards  and protocols for validation of devices manufactured via the synthetic route.

Requirements:

·       Degree-qualified in science or engineering (ideally chemistry or analytical science).

·       Possess a minimum 5 years of experience in process validation applied in pharmaceutical or medical device industry

 

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