Senior Quality Leader – Biologics GMP, On-Site
Listed on 2026-10-31
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Scorpion Therapeutics seeks an Associate Director of Quality to oversee site compliance within a biopharma manufacturing environment. The role focuses on maintaining regulatory standards and driving continuous quality improvement.
You will provide quality direction, manage critical documentation, and lead audits to ensure GMP compliance. The position also leads quality systems including change control and supervises Quality Specialists working with operations teams.
Consider building your career as a Senior Quality Leader – Biologics GMP, On-Site at Merck.
All applications are reviewed carefully by our team.
The position is based in PA, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Management & Operations.
The advertised compensation is 140..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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