QC Raw Materials Supervisor
Core
Leads laboratory teams to perform testing of pharmaceutical utilities (air, gas, water), manage quality deviations, and ensure compliance with cGMP in cleanroom environments.
Role type
Senior IC QC Raw Materials Supervisor with leadership responsibilities
Builds
Production quality data and compliant laboratory operations for pharma clients
Domain
Pharmaceutical manufacturing and quality control
Required skills
GMP compliance, sterile gowning/aseptic techniques, instrument calibration, quality deviation investigation, team leadership, training coordination, document control (SOPs/batch records), resource planning
Preferred skills
ISO 8 cleanroom experience, method validation
Technologies
Laboratory information management systems (LIMS), analytical instruments
Responsibilities
Calibrate instruments, investigate quality deviations, lead and train direct reports, review controlled documents, plan workloads, monitor team performance against metrics
Seniority
Senior, hands-on IC with team leadership
