As the Head of QA, You will be candidate will be responsible for leading the manufacturing QA team and assuring the sites compliance with GxP regulations.
Key responsibilities within the position will be to (Not limited to):
The ideal candidate for this opportunity will have previous experience leading a Quality Assurance function, within a pharmaceutical sterile manufacturing site. You will also have strong knowledge of GxP regulations / industry expectations for Quality Management System processes and associated systems, especially MHRA Guidance for Specials Manufacture.
If you are interested in this opportunity, please send your up-to-date CV to [email protected] or call Addison on 02392 322338.
STR Limited is acting as an Employment Agency in relation to this vacancy.
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