GMP QA Documentation Specialist
Listed on 2026-10-06
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Regulatory Compliance Specialist
Bimeda is seeking a QA Documentation Specialist to maintain site QA/QMS documentation and oversee archival processes in a regulated environment. You will review release documentation, manage SOPs, and contribute to batch release activities with a focus on accuracy and compliance.
The role involves handling CoC/CoA generation, packaging specifications, and line setup approvals. Strong analytical skills and meticulous attention to detail are essential for success.
The GMP QA Documentation Specialist position in the Engineering field is open for applications.
The position is based in Wales, United Kingdom.
This opportunity is part of our work in Engineering.
The advertised compensation is 35.000 - 50.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the GMP QA Documentation Specialist role in the description above.
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