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).

- Strong 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)
🏢 Pramukh Staffing
📍 Amreli