Demo

Production Supervisor

Piramal Pharma Solutions
Bethlehem, PA Full Time
POSTED ON 9/30/2025
AVAILABLE BEFORE 11/30/2025

Essential Duties and Responsibilities

  • First line responsibility for the safe operation of chemical operations, the manufacturing process and all operations, maintenance or work taking place during their shift
  • Direct the appropriate response to a safety incident or other emergency until the emergency chain of command arrives
  • Reinforce and ensure plant safety practices and maintain a constant alert for hazardous conditions on a daily basis.
  • Lead/Participate in Incident and Discrepancy Investigations as necessary
  • Responsible for the proper issuance of any work permits, including Lockout/Tag Out
  • Keep Production Supervisors and Management informed as to the state of operations and production needs that need to be addressed
  • Address substandard performance in a fair and timely manner
  • Responsible for ensuring efficient operations to meet production demands and schedules
  • Lead improvement projects within the plant
  • Responsible for the organization and cleanliness of the production floor
  • Identify when modifications to SOP’s are necessary for safety reasons, quality concerns, or operational efficiency
  • Identify and potentially assist with maintenance repairs
  • Responsible for the daily scheduling, and maintaining vacation time records for operators on the crew
  • Assign overtime as required to meet production requirements
  • Communication with vendors for ordering, pick up, and delivering of materials
  • Train operators on proper operation, maintenance, safety, proper system set-up and housekeeping requirements for assigned tasks
  • Responsible for proper production startups, shutdowns and changeovers
  • Ensure accurate production logs are kept on a daily basis, including an accurate shift supervisors log of all events occurring on shift
  • Coordinate with Manufacturing and Maintenance personnel for maintenance work on equipment needing to be done
  • Review of Manufacturing batch records to ensure completeness and accuracy before submission to Quality Assurance
  • Drive cGMP standards within the Manufacturing area including training of operators
  • Work with QA and QC to ensure process and materials meet all quality specifications
  • Lead SFTI/5S efforts in the Manufacturing area and support associated projects and improvements

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