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Third Shift - Manufacturing Supervisor

Job

Sharp Sterile Manufacturing

Becket, MA (In Person)

Full-Time

Posted 6 days ago (Updated 1 day ago) • Actively hiring

Expires 6/22/2026

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Job Description

Third Shift - Manufacturing Supervisor at Sharp Sterile Manufacturing Third Shift - Manufacturing Supervisor at Sharp Sterile Manufacturing in Becket, Massachusetts Posted in 3 days ago.
Type:
full-time
Job Description:
The 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 procedures Maintain and report metrics to evaluate performance of assigned manufacturing unit Compile area specific shift information and accurately convey information to oncoming shifts, management team and support groups Maintain and support metrics to evaluate performance of assigned shift Provide technical expertise in component preparation, formulation and filling and visual inspection. Support operational and preventive maintenance of area specific processing equipment Report and investigate Quality deviations and events Report and participate in the investigation of safety incidents Act in place of manufacturing manager in their absence Demonstrate BSM values and behaviors at all times Attend and complete all mandatory training Maintain continued education and proficiency in field through education, literature and seminars Other duties as assigned Carryout all duties in compliance with regulatory and professional agencies, including but not limited to state, FDA, OSHA and EU regulations, or otherwise as applicable Directly supervise four (4) to eight (8) team members to include: interviewing, hiring and training employees planning, assigning and directing work appraising performance rewarding and disciplining employees addressing complaints and resolving problems Familiar with cGMP regulations and principles and how to apply them to the manufacturing of pharmaceutical/biotech products
Requirements:
Three (3) years related pharmaceutical production operations experience within component preparation, formulation, filling and visual inspection or proven ability of same Prior supervisory experience a plus Bachelor's degree preferred An equivalent combination of education and experience may be considered

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