Role Overview
Supervise and oversee all compression operations in a US FDA‑approved 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 Pharmaceutical Industries
📍 Dadra