QC Pharma Projects Lead - GMP Lab Oversight
Listed on 2026-10-27
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Abb Vie is seeking a QC Pharma Projects Supervisor for a 12-month fixed-term assignment at our Westport site. You will lead a team of 8-12 staff within Projects, overseeing QC activities in cleaning validations, residual monitoring and method transfers to QC.
The role requires strong leadership, GMP expertise and cross-functional collaboration. Responsibilities include guiding reports, maintaining regulatory alignment, and driving performance, training, and succession planning.
The QC Pharma Projects Lead - GMP Lab Oversight role at Abb Vie Inc. is now open for applications in MO, United States.
The position is based in MO, United States.
This opportunity is part of our work in Management & Operations, Engineering.
The advertised compensation is 75..
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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