Senior - Officer Compression Block A

Sun Pharmaceutical Industries, Inc.; India; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Sun Pharmaceutical Industries Ltd. seeks a Senior - Officer Compression to supervise tablet compression lines at a US FDA‑approved OSD manufacturing plant in Dadra.

You will ensure cGMP compliance, oversee staffing across shifts, and coordinate with QA/QC and maintenance teams to meet production goals. The role requires 3–5 years in OSD compression with 1–2 years in supervision, and strong knowledge of cGMP, FDA 21 CFR Part 211, and data integrity principles.

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.

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.

Skills

cGMP

FDA 21 CFR Part 211

Data integrity

Leadership

Documentation

Team supervision

Quality control

Education

Bachelor’s in Pharmacy

Job description

Select how often (in days) to receive an alert: Create Alert

Title: Senior - Officer Compression Block A

Date: Aug 26, 2026

Location: Dadra 1 - Operations Block A

Company: Sun Pharmaceutical Industries Ltd

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 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.