Third Shift - Manufacturing Supervisor
Occupations:
First-Line Supervisors of Production and Operating WorkersIndustrial Production ManagersQuality Control Systems ManagersFirst-Line Supervisors of Helpers, Laborers, and Material Movers, HandFirst-Line Supervisors of Material-Moving Machine and Vehicle OperatorsIndustries:
Pharmaceutical and Medicine ManufacturingOther Textile Product MillsOther Nonmetallic Mineral Product ManufacturingIndustrial Machinery ManufacturingMedical Equipment and Supplies ManufacturingThe Manufacturing Supervisor supports and directs /Manufacturing Leads and Associates in the formulation, filling, component prep and visual inspection of sterile, injectable biological products within the production and quality goals set by management. Oversee personnel and activities related to the production process ensuring compliance with cGMPs and BSM-specific policies and proceduresMaintain and report metrics to evaluate performance of assigned manufacturing unitCompile area specific shift information and accurately convey information to oncoming shifts, management team and support groupsMaintain and support metrics to evaluate performance of assigned shiftProvide technical expertise in component preparation, formulation and filling and visual inspection.Support operational and preventive maintenance of area specific processing equipmentReport and investigate Quality deviations and eventsReport and participate in the investigation of safety incidentsAct in place of manufacturing manager in their absence Demonstrate BSM values and behaviors at all timesAttend and complete all mandatory training Maintain continued education and proficiency in field through education, literature and seminarsOther duties as assignedCarryout all duties in compliance with regulatory and professional agencies, including but not limited to state, FDA, OSHA and EU regulations, or otherwise as applicableDirectly supervise four (4) to eight (8) team members to include: interviewing, hiring and training employees planning, assigning and directing work appraising performancerewarding and disciplining employeesaddressing complaints and resolving problemsFamiliar with cGMP regulations and principles and how to apply them to the manufacturing of pharmaceutical/biotech productsRequirements:Three (3) years related pharmaceutical production operations experience within component preparation, formulation, filling and visual inspection or proven ability of samePrior supervisory experience a plusBachelor’s degree preferredAn equivalent combination of education and experience may be considered