Senior - Officer Compression Block A

Sun Pharma; Dadra and Nagar Haveli; On-site; INR 1,400,000 - 2,100,000; Full time

Job summary

Sun Pharma in India seeks a seasoned supervisor to oversee tablet compression lines in an OSD manufacturing plant, ensuring operations meet cGMP and FDA standards while achieving production goals.

You will supervise daily compression, allocate shifts, coordinate with QA/QC, monitor in-process checks, and handle changeovers, maintenance, and documentation. This role demands leadership, strong problem-solving, and a commitment to data integrity and safety across the compression area.

Qualifications

• OSD compression experience with focus on cGMP and FDA guidelines.
• 1–2 years in a supervisory role and strong documentation skills.
• Knowledge of data integrity principles and regulatory requirements.

Responsibilities

• Supervise daily tablet compression operations per cGMP and FDA guidelines.
• Allocate manpower across shifts and manage production schedules.
• Coordinate with QA/QC for line clearance and documentation accuracy.
• Monitor in-process checks (weight, hardness, thickness, friability) and address deviations.
• Oversee equipment setup, cleaning, and preventive maintenance.
• Train operators on equipment handling and safety protocols.
• Prepare daily production reports and escalate issues to management.

Skills

Leadership

Problem-solving

Documentation

cGMP knowledge

FDA 21 CFR Part 211

Data integrity

Education

Bachelor’s in Pharmacy

Job description

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 elevate 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.