About The Position

The Group Lead is responsible for leading the manufacturing process for batches and demonstrating the methods and procedures used to produce products with state-of-the-art processing systems, including sophisticated recipe-controlled human-machine interface (HMI) control systems. The role coordinates production workflow and personnel while ensuring manufacturing and packaging activities comply with cGMP standards, CAPAs, and SOPs. The Group Lead verifies product and packaging components, checks products and labels against specifications and production records, maintains accurate documentation, and ensures label reconciliation and reviewed records are submitted to Quality Assurance. The role also oversees equipment readiness and use, material status, room cleanliness, and safe handling of rejected materials. This is a night-shift position.

Requirements

  • High school diploma or GED.
  • At least 3 years of manufacturing experience in the pharmaceutical or medical device industry.
  • At least 1 year of experience leading a team, coordinating workflow, and supporting daily production activities.

Responsibilities

  • Verify all product and packaging/manufacturing components before operations begin and before entering the packaging room.
  • Check and confirm products, ousters, and labels against specifications in the batch record, work order, and packaging record.
  • Ensure accurate logbook data entry and completion of documentation for each batch.
  • Initiate batch records according to the production schedule and verify staging status for upcoming batches on each line.
  • Print and inspect shipper case labels for accuracy.
  • Ensure 100% label reconciliation, verify results against the vision system report, and submit reviewed documentation to Quality Assurance promptly.
  • Follow the manufacturing schedule based on the shipping forecast and ensure manufacturing components have proper status identification throughout the process.
  • Dispose of rejected materials and packaging components according to established procedures.
  • Verify equipment calibration status before use.
  • Set up, operate, and clean equipment in compliance with cGMP standards.
  • Complete ROSS transactions promptly and schedule personnel to support efficient operations across manufacturing rooms.
  • Adhere to Amneal Packaging CAPAs and Standard Operating Procedures (SOPs).
  • Wear appropriate safety and protective gear and comply with dress code requirements.
  • Maintain focus to prevent mix-ups and cross-contamination.
  • Keep rooms clean, organized, and compliant.
  • Perform other duties as assigned.

Benefits

  • Short-term incentive opportunity, such as a bonus or performance-based award.
  • Long-term incentive award, such as restricted stock units.
  • Health and insurance benefits for eligible positions.
  • 401(k) matching contribution.
  • Employee well-being programs.
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