Responsibilities

• Execute production as per batch record, SOPs, and schedule.
• Ensure GMP/cGMP compliance, safety, cleanliness, and correct in-process checks.
• Maintain accurate batch documentation and traceability (materials, batch/lot, checklists).
• Coordinate with QC/QA for in-process testing, batch status, and deviations support.
• Monitor line/equipment performance, handle changeovers, and reduce downtime/rejections.
• Support investigations (deviation/OOS if applicable) and CAPA/continuous improvement.

Requirements

• Bachelor’s in Pharmacy/Life Sciences/Engineering or equivalent.
• 2–6 years production experience in pharma/supplement/medical manufacturing.
• Strong knowledge of GMP and manufacturing documentation.