Job Description

Key Responsibilities:

Supervise and execute production activities in the formulation department as per batch manufacturing records (BMR) and standard operating procedures (SOPs). Ensure compliance with cGMP, GDP, and regulatory requirements during manufacturing. Handle granulation, compression, coating, and packing activities in oral solid dosage (OSD) . Maintain proper documentation (BMR, BPR, logbooks, cleaning records, online entries). Monitor in-process checks (IPQC) to ensure product quality and yield. Coordinate with QA, QC, Engineering, and Warehouse for smooth execution of production. Train operators and workers on SOPs, safety, hygiene, and GMP practices. Support scale-up, validation, and new product introduction activities. Ensure optimum utilization of manpower, machines, and materials. Report deviations, incidents, or breakdowns to seniors and assist in CAPA implementation.

Key Skills & Competencies:

Knowledge of formulation manufacturing processes (granulation, compression, coating, encapsulation, etc.). Good understanding of cGMP, GDP, and regulatory guidelines (USFDA, MHRA, WHO, etc.). Strong documentation and compliance skills. Ability to handle equipment like RMG, FBD, Compression Machine, Coating Machine, Blister Packing, etc. Leadership and team-handling abilities. Strong problem-solving and decision-making skills.

Qualification & Experience:

Education:

B.Pharm / M.Pharm / B.Sc. / M.Sc. in relevant field.

Experience:

1-5 years (Officer) / 3-7 years (Executive) in pharmaceutical formulation production.
Job Type: Full-time

Pay: ₹18,445.96 - ₹30,000.96 per month

Benefits:

Cell phone reimbursement Internet reimbursement Paid sick time Provident Fund
Application Deadline: 01/10/2025