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.


·       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


Upload your CV/resume or any other relevant file. Max. file size: 256 MB.
Check the box to confirm our use of your data under GDPR regulations. To register your CV you must tick the checkbox to confirm your acceptance of our GDPR and Privacy Policy