Role Overview

Supervise and oversee all compression operations in a US FDAapproved Oral Solid Dosage (OSD) manufacturing plant. Ensure tablet compression lines meet cGMP, FDA standards, and production goals.

Key Responsibilities

- Supervise daily tablet compression operations as per cGMP and FDA guidelines.

- Manage and allocate manpower across shifts for smooth production.

- Ensure compliance with SOPs, batch records, and regulatory requirements.

- Monitor in-process checks (weight, hardness, thickness, friability) and resolve deviations.

- Oversee equipment setup, cleaning, and preventive maintenance.

- Coordinate with QA/QC for line clearance and documentation accuracy.

- Handle changeovers and ensure timely completion of production schedules.





- Train and guide operators on equipment handling and safety protocols.

- Maintain housekeeping and safety standards in compression area.

- Prepare daily production reports and escalate issues to management.

Qualifications

- Bachelor’s in Pharmacy or related field.

- 3–5 years experience in OSD compression; 1–2 years in supervisory role.

- Robust knowledge of cGMP, FDA 21 CFR Part 211, and data integrity principles.

- Leadership, problem-solving, and documentation skills.

📌 Senior - Officer Compression Block A (Dadra)
🏢 SUN PHARMA
📍 Dadra