Job Description

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.
• Strong knowledge of cGMP, FDA 21 CFR Part 211, and data integrity principles.
• Leadership, problem-solving, and documentation skills.

Skills Required