Description
An exciting opportunity for an experienced QA/Validation Engineer to become part of a team performing a Supplier Quality review of processing equipment and devices used in the manufacture of Pharmaceuticals and Bio-pharmaceutical products.You will be involved in identifying where data is missing and making contact with the various suppliers to expedite the missing information.
Skills and experience required:
*Strong background within Pharmaceutical or Bio-pharmaceutical manufacturing to include GMP and QA experience
*Experience in generating SOP’s
*Compliance experience with: ISO, USP,FDA and/or REACH
*Prior experience with sourcing missing QA and technical data from suppliers
*Ideally previous experience in mechanical or plastics or polymers
This challenging opportunity would suit an experience QA or QAV consultant who is looking to broaden their experience within a leading Life Sciences organisation