Job Description

Title:

Executive - OSD Production

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Date: Dec 18, 2025
Location: Dadra 1 - Operations Block B
Company: Sun Pharmaceutical Industries Ltd

Job Purpose:

To oversee and manage day-to-day production activities in the Oral Solid Dosage (OSD) manufacturing area, ensuring compliance with cGMP, USFDA, and other regulatory requirements while meeting production targets.

Key Responsibilities:

Supervise and execute production operations for granulation, compression, coating, and capsule filling. Ensure adherence to batch manufacturing records (BMR) and standard operating procedures (SOPs). Monitor in-process checks (IPC) and ensure compliance with quality standards. Coordinate with QA, QC, Engineering, and Warehouse departments for smooth production flow. Ensure proper documentation and compliance with USFDA, MHRA, and other regulatory guidelines. Train and guide operators and technicians on GMP practices and safety protocols. Participate in investigations of deviations, change controls, and CAPA implementation. Monitor equipment performance and coordinate with maintenance for preventive and breakdown maintenance. Ensure proper material reconciliation and yield monitoring. Maintain hygiene and safety standards in the production area.

Key Requirements:

Education:

B.Pharm / M.Pharm in a relevant field.

Experience:

5 - 7 years in OSD production in a USFDA/MHRA-approved facility.

Skills:

Strong knowledge of cGMP, GDP, and regulatory compliance. Hands-on experience in granulation, compression, coating, and encapsulation. Good documentation and communication skills. Ability to handle audits and regulatory inspections.

Preferred Qualifications:

Experience with SAP or other ERP systems. Exposure to regulatory audits (USFDA, MHRA, WHO, etc.). * Certification in GMP or production management is a plus.