QA Documentation Specialist; GMP/QMS
Listed on 2026-10-07
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Regulatory Compliance Specialist, Data Analyst
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.
We have an opening for a QA Documentation Specialist (GMP/QMS) in United Kingdom within Bio & Pharmacology & Health.
We appreciate your interest in this position.
Join Bimeda, Inc. and contribute to our ongoing work.
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This posting is for the QA Documentation Specialist (GMP/QMS) role at Bimeda, Inc., based in United Kingdom.
We are looking to fill the QA Documentation Specialist (GMP/QMS) position at Bimeda, Inc. in United Kingdom.
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