Bimeda is seeking a QA specialist in the United Kingdom to effectively maintain site QA / QMS documentation systems and QC testing activity for materials and finished product.
The role covers review of release documentation, management of the retain room, SOP development support, and generating CoC/CoA for batches, while ensuring GMP/GDP and cGMP compliance across packaging and production records.
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QA Documentation Specialist (GMP/QMS) employer: Bimeda, Inc.
Bimeda is an excellent employer that values its employees by fostering a collaborative and innovative work culture at our Beaverdale, Cambridge facility. We offer competitive benefits, opportunities for professional growth, and a commitment to continuous improvement, making it a rewarding environment for those looking to make a meaningful impact in aseptic manufacturing.
