QA Specialist - cGMP Compliance & SOP Champion
Listed on 2026-10-06
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Quality Assurance - QA/QC
Data Analyst -
Healthcare
Data Scientist
A chez Avecia Pharma, the Quality Assurance Specialist will document and audit cGMP practices across the site, developing and revising QA procedures to strengthen cGMP compliance per USFDA Title 21 CFR Part 210, 211 and ICH Q7 guidance.
Key responsibilities include coordinating with departments to meet GMP requirements, approving SOPs, and ensuring batch records and QC docs meet quality standards. The role emphasizes liaison with clients and cross-functional collaboration.
We have an opening for a QA Specialist I - cGMP Compliance & SOP Champion in Cincinnati, OH, United States within Management & Operations.
Are you ready to take on the QA Specialist I - cGMP Compliance & SOP Champion role at Avecia Pharma?
We would love to welcome a new QA Specialist I - cGMP Compliance & SOP Champion to our team in Cincinnati, OH, United States.
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