Role & responsibilities

- Supervise daily tablet compression operations.
- Ensure production schedules are met according to the manufacturing plan.
- Monitor tablet quality parameters such as weight variation, hardness, thickness, friability, and appearance.
- Ensure compliance with GMP, SOPs, data integrity, and regulatory guidelines.
- Coordinate with Production Planning, Quality Assurance (QA), Quality Control (QC), Engineering, and Warehouse departments.
- Verify line clearance before batch initiation.
- Review and maintain Batch Manufacturing Records (BMRs) and production documentation.
- Investigate production deviations, non-conformances, and implement corrective and preventive actions (CAPA).
- Optimize machine utilization and minimize downtime.
- Ensure proper operation, cleaning, and maintenance of tablet compression machines.




- Train and develop operators and production staff.
- Monitor productivity, yield, and process efficiency.
- Participate in validation, qualification, and process improvement activities.
- Ensure compliance with EHS (Setting, Health & Safety) standards.

Preferred candidate profile

- Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, or a related field.
- 58 years of experience in pharmaceutical tablet manufacturing, with at least 2 years in a supervisory role.
- Knowledge of tablet compression machines (e.g., Fette, Korsch, Cadmach, or GEA).
- Strong understanding of GMP, cGMP, FDA, MHRA, EU GMP, and WHO guidelines.
- Experience in documentation, audits, and regulatory inspections.

📌 Compression Assistant Manager (Baddi)
🏢 Acme Generics
📍 Baddi