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Now viewing: 3rd Shift Manufacturing Supervisor
ML
Meet Life Sciences
3rd Shift Manufacturing Supervisor
Job Description
3rd Shift Manufacturing Supervisor at Meet Life Sciences 3rd Shift Manufacturing Supervisor at Meet Life Sciences in Arlington, Massachusetts Posted in 6 days ago.
Lead and support four contract manufacturing associates; assign tasks and provide coachin g.
Ensure production suites, equipment, and materials are ready and complian t.
Enforce cGMP, safety, and quality standard s.
Review batch records and documentation for accuracy and completenes s.
Execute shift schedules to meet production timeline s.
Escalate and support resolution of manufacturing issues, deviations, CAPAs, and change control s.
Support new processes, SOP implementation, and technology transfer s.
Provide clear shift handovers and communicate production status and risk s. Qualificati onsBachelor's degree in Biology, Biochemistry, Engineering, or related field preferr ed.3-6 years of GMP manufacturing experience; prior supervisory or lead experience preferr ed.
Experience with fermentation, microbial processing, aseptic techniques, or lyophilization preferr ed.
Strong knowledge of cGMP regulations and documentation practic es.
Experience reviewing batch records and supporting deviation manageme nt.
Type:
full-timeJob Description:
•3rd shift, 11pm-7:30am• Job Summar yThe Manufacturing Supervisor provides hands-on leadership of second shift GMP manufacturing operations for microbiome Live Biologic Products. This role supervises four contract associates and ensures safe, compliant, and efficient execution of fermentation, harvest, lyophilization, media/buffer preparation, packaging, and suite readiness activities. The Supervisor serves as the primary on-site manufacturing leader during second shift and actively supports floor operations . Responsibiliti esSupervise third shift GMP manufacturing activities, including fermentation and downstream processin g.Lead and support four contract manufacturing associates; assign tasks and provide coachin g.
Ensure production suites, equipment, and materials are ready and complian t.
Enforce cGMP, safety, and quality standard s.
Review batch records and documentation for accuracy and completenes s.
Execute shift schedules to meet production timeline s.
Escalate and support resolution of manufacturing issues, deviations, CAPAs, and change control s.
Support new processes, SOP implementation, and technology transfer s.
Provide clear shift handovers and communicate production status and risk s. Qualificati onsBachelor's degree in Biology, Biochemistry, Engineering, or related field preferr ed.3-6 years of GMP manufacturing experience; prior supervisory or lead experience preferr ed.
Experience with fermentation, microbial processing, aseptic techniques, or lyophilization preferr ed.
Strong knowledge of cGMP regulations and documentation practic es.
Experience reviewing batch records and supporting deviation manageme nt.