Hands-On QA Manager, cGMP Peptide Manufacturing
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
Job Description & How to Apply Below
CSBio Co. in Milpitas, CA seeks a hands-on Quality Assurance Manager to supervise daily QA activities supporting peptide manufacturing and cGMP compliance. You will manage QA staff and review deviations, CAPAs, change controls, training, batch records, audits, and inspections.
The role partners with Manufacturing, QC, Materials, Facilities, Regulatory, and management to resolve quality issues and maintain readiness for regulatory inspections.
We are currently recruiting a Hands-On QA Manager, cGMP Peptide Manufacturing for our team in Milpitas, CA, United States.
This opportunity is part of our work in Finance, Engineering.
The advertised compensation is 120..
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 Hands-On QA Manager, cGMP Peptide Manufacturing role in the description above.
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