Apply Now »

Title:  Executive

Date:  Oct 6, 2026
Location:  Pithampur (MP)
Company:  Sun Pharmaceutical Industries Ltd

 

Job Title:

Manufacturing Supervisor – Production    

Business Unit:

Sun Global Operations

Job Grade

G12A

Location :

Pithampur

 

 

 

Responsibilities

  1. Supervise day-to-day sterile injectable manufacturing operations, including compounding, filtration, filling, sealing, and other aseptic processes.
  2. Ensure manufacturing activities are executed as per production plans, approved Batch Manufacturing Records, SOPs, cGMP, and regulatory requirements.
  3. Monitor critical process parameters, production output, yield, rejection, equipment performance, and achievement of production targets.
  4. Ensure line clearance, area readiness, material availability, equipment readiness, and adherence to contamination-control practices.
  5. Handle QMS activities such as deviations, CAPA, change controls, incident investigations, risk assessments, and root-cause analysis.
  6. Review Batch Manufacturing Records, equipment logbooks, area records, and other GMP documents for accuracy and completeness.
  7. Perform and review SAP transactions related to production orders, material issuance, consumption, reconciliation, yield, and batch confirmation.
  8. Participate in equipment procurement, preparation of User Requirement Specifications, technical evaluation, installation, commissioning, and qualification activities.
  9. Coordinate DQ, IQ, OQ, PQ, process validation, cleaning validation, equipment requalification, and preventive maintenance activities.
  10. Coordinate with vendors for equipment installation, maintenance, technical services, spare parts, and timely completion of assigned activities.
  11. Collaborate with QA, QC, Engineering, Warehouse, Planning, Validation, and EHS teams to ensure smooth manufacturing operations.
  12. Supervise and train officers, technicians, operators, and contractual employees on SOPs, cGMP, aseptic practices, documentation, equipment operation, and safety.
  13. Support internal, customer, and regulatory audits by maintaining manufacturing areas and documentation in an audit-ready condition.
  14. Drive continuous improvement initiatives focused on productivity, process reliability, yield improvement, cost optimisation, waste reduction, and equipment efficiency.

Travel Estimate

 

Job Requirements

Education Qualification

B.Pharma /M.Pharma/M.Sc.

Experience

Tenure:  6+ Years

Your Success Matters to Us

 

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!

 

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification.  It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job.  Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

           

 

Apply Now »