Supervisor I, QC Lab
Core
Organizing, administering, and supervising lab analysts to oversee chemical analysis and release of raw materials, in-process, and final products in compliance with quality criteria.
Role type
QC Lab Supervisor I
Builds
Production quality data and compliant product releases
Domain
Pharmaceutical manufacturing / Quality Control
Deliverable
production ML models | product features | dashboards & analysis | client delivery | infrastructure | physical/clinical work
Required skills
cGMP compliance, analytical laboratory equipment operation, laboratory operations management, data review and approval, corrective action implementation, team leadership, training administration, instrumentation maintenance planning, waste management, audit support
Preferred skills
Scientific background in Chemistry, Microbiology, or Biology, problem-solving, cross-functional coordination
Technologies
Analytical/microbial instrumentation
Responsibilities
Lead and develop a high-performing team including hiring, coaching, and performance feedback; oversee laboratory group operations for raw materials, finished products, and environmental monitoring; review and approve analytical data; support investigations of out-of-specification results; communicate QC metrics and lead Tier meetings; ensure procedures align with cGMP and safety standards; assist with instrumentation maintenance and qualification; inspect laboratory facilities for GMP compliance; manage hazardous and non-hazardous waste.
Seniority
Individual Contributor, supervisory level