Job Description:
Oversee day-to-day production activities for formulation batches as per approved BMR/BPR.
Ensure compliance with cGMP, GDP, and regulatory guidelines (WHO, EU, USFDA, MHRA as applicable).
Monitor production planning, batch scheduling, material requirement, and manpower allocation.
Coordinate with QA, QC, Warehouse, Engineering, and RA for smooth production operations.
Review and ensure timely completion of batch documentation and deviation/incident reports.
Supervise equipment operation, cleaning, and validation activities.
Maintain discipline, safety practices, and 5S in the production area.
Identify process gaps and implement improvements (CAPA, process optimization, yield improvement).
Train operators and team members on SOPs, safety, and GMP practices.




Support audits (internal and external) by providing documents and ensuring compliance readiness.

Required Skills:
B.Pharm / M.Pharm / B.Sc / M.Sc or relevant qualification.
5–10 years of hands-on experience in formulation production (OSD / Liquid / Injectable – specify).
Solid knowledge of machines like RMG, FBP, Compression, Coating, Blister/Strip packing (as per plant type).
Excellent understanding of GMP, documentation, and regulatory standards.
Solid leadership, communication, and team-handling skills.
Ability to manage multiple batches and meet production targets.

📌 Production Assistant Manager For Pharmaceutical Company Amreli (India)
🏢 Pramukh Staffing
📍 India