Lead QC Pharma Projects - GMP Analytical Excellence
Listed on 2026-10-19
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Quality Assurance - QA/QC
Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Abb Vie is hiring a QC pharma projects supervisor for a fixed-term period of 12 months at its Westport site. The role leads a team of 8-12 in the Projects team, overseeing QC activities supporting operations cleaning validations, residual monitoring, and method transfers to QC laboratory.
The candidate should have a science degree and 3+ years in GMP/GLP analytical labs with proven team leadership, plus hands-on experience with HPLC/GC and Empower software.
The following role is for a Lead QC Pharma Projects - GMP Analytical Excellence with ABBVIE.
Full responsibilities and requirements are described in the listing above.
Learn more about the Lead QC Pharma Projects - GMP Analytical Excellence role in the description above.
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