Center Quality Manager – GMP Compliance & Audits
Listed on 2026-10-15
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
ADMA Biologics, Inc. in Hammond, LA seeks a Manager, Center Quality to lead QA activities at donor center operations.
The role emphasizes ensuring compliance with cGMP requirements, supervising QA specialists, and the ability to authorize product releases and stop shipments when necessary. Strong data, regulatory, and leadership skills are essential. You will coordinate audits, develop policies, and drive process improvements in a fast-paced biopharmaceutical manufacturing environment.
We are currently recruiting a Center Quality Manager – GMP Compliance & Audits for our team in Hammond, LA, United States.
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 Center Quality Manager – GMP Compliance & Audits role in the description above.
We appreciate your interest in this position.
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