Manufacturing Supervisor
Listed on 2026-10-08
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Manufacturing / Production
Pharmaceutical Manufacturing, Validation Engineer, Manufacturing & Industrial Operations
Manufacturing Supervisor overseeing Upstream/Cell Culture in a cGMP Biologics manufacturing facility.
ResponsibilitiesManaging personnel, ensuring adherence to SOPs and cGMP regulations, monitoring manufacturing processes, documentation, training, and supporting deviations and investigations. The role involves coordinating with support functions like validation and facilities, troubleshooting equipment issues, and developing team goals.
QualificationsBachelor's (preferred) or associate degree with 4+ or 6+ years of GMP experience respectively, or high school diploma with 8+ years in GMP. Prior supervisory experience and strong knowledge of biologics manufacturing, including equipment operation and troubleshooting, are required.
SkillscGMP/GDP application, scientific understanding of biologics, and proficiency in MS Office.
Cross-Functional CollaborationMay involve cross-functional collaboration with QC, Regulatory, QA, and Materials Management.
High-value specificsBiologics manufacturing, upstream/cell culture, GMP compliance, deviation management, and process troubleshooting.
LocationBrooklyn Park, MN.
TravelNot specified.
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