Supervisor I, QC Lab

Role: QC Lab Supervisor I overseeing laboratory operations, team management, and analytical testing to ensure compliance with cGMP and quality standards in biopharma manufacturing. Responsibilities: lead and develop a high-performing team, manage daily lab activities across raw materials, in-process, and final product testing; review and approve analytical data; support investigations, CAPAs, and continuous improvement initiatives; ensure instrument availability and maintenance; maintain audit readiness and compliance with safety regulations. Qualifications: Bachelor's in Chemistry, Microbiology, or Biology; 2+ years of QC Laboratory experience; strong knowledge of analytical techniques, GMP regulations, and laboratory systems; effective problem-solving, leadership, and cross-functional collaboration skills. High-Value: Biopharma quality control, GMP compliance, analytical chemistry, microbiology, lab operations, and investigations; applicable to manufacturing of biologics, small molecules, or cell/gene therapies. Work setup: not explicitly stated, but likely on-site given supervisory and GMP oversight duties.