Job Description

Key Responsibilities (JD Snippet):

Shift Management:

Oversee all tablet manufacturing (granulation, compression, coating, packing) during shifts, managing manpower and resources to meet targets.

GMP & Documentation:

Ensure strict adherence to cGMP (current Good Manufacturing Practices), prepare/review BMRs/BPRs, and maintain clean/calibrated equipment.

Quality Control:

Verify raw material dispensing, check process parameters, coordinate with QC for testing, and initiate investigations for deviations.

Equipment & Maintenance:

Monitor equipment performance, coordinate with engineering for breakdowns, and ensure cleaning protocols are followed.

Coordination:

Liaise with QC, Engineering, and Warehouse for materials, testing, and breakdowns.

Training:

Ensure team follows SOPs, safety protocols, and hygiene standards.
Core Duties & Tasks:

Execute production steps: Dispensing, blending, granulation, drying, compression, coating, packing. Complete & review Batch Manufacturing Records (BMRs) and Batch Packing Records (BPRs). Perform & record daily/monthly equipment calibration checks (e.g., weighing balances). Manage change parts (punches, dies, sieves). Initiate & manage Change Controls, Deviations, and Investigations (Failure, Market Complaint). Monitor & record environmental conditions (Temp, Humidity, DP) in clean areas. Ensure good housekeeping and safe working conditions.
Essential Skills & Qualifications:

Education:

B.Pharm, B.Sc., D.Pharm, M.Sc..

Experience:

1-5 years in pharma production (granulation, compression).

Knowledge:

cGMP, SOPs, QMS (Quality Management Systems).
Job Types: Full-time, Permanent

Pay: Up to ?25,000.00 per month

Benefits:

Food provided Health insurance Leave encashment Paid sick time Provident Fund
Work Location: In person