QC Pharma Projects Lead - GMP Analytics & Validation

AbbVie Westport is seeking a QC Pharma Projects Supervisor for a 12-month fixed-term contract to lead a 8-12 person Projects team within QC.

The role oversees operations including cleaning validations, residual monitoring and method transfers to the QC laboratory, ensuring GMP/compliance and timely delivery while coaching staff and coordinating with multiple stakeholders across QA and manufacturing.