Pharma Manufacturing QA Site Supervisor (Must have API Pharma Exp/ Strong in QA Site Work) Up 12K HJC
Core
Lead on-site quality assurance activities in manufacturing, packaging, and warehouse areas to ensure GMP compliance and manage material release and cleaning validation.
Role type
Senior IC QA Site Supervisor
Builds
Pharmaceutical products and packaging materials
Domain
Pharmaceutical manufacturing (API)
Required skills
GMP compliance, material release management, cleaning validation, deviation investigation, CAPA management, regulatory inspection coordination, team leadership, data integrity, risk assessment
Preferred skills
Experience with PIC/S, EU GMP, FDA cGMP, WHO guidelines, cross-functional collaboration
Technologies
GMP, QMS, HSA regulations
Responsibilities
Lead and manage on-site quality assurance activities to ensure compliance with GMP and regulatory requirements; Review and approve documentation supporting the release of raw and packaging materials; Establish and maintain the site cleaning validation program; Lead investigations of deviations, incidents, and change controls; Coordinate preparation for customer audits and regulatory inspections; Manage Site QA team performance and training.
Seniority
Senior, hands-on IC