executive

SUN PHARMA

Dhar

On-site

INR 700,000 - 1,100,000

Full time

41 hours ago
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Job summary

Sun Pharma, Sun Global Operations in Pithampur, seeks a Manufacturing Supervisor - Production to oversee sterile injectable manufacturing operations and ensure adherence to production plans and GMP standards.

Lead a team of officers, technicians, operators, and contract staff while focusing on quality, process reliability and continuous improvement. Strong collaboration with QA, QC, Engineering, and EHS is required.

Qualifications

  • B.Pharma /M.Pharma / M.Sc. required.
  • 6+ years of experience in manufacturing supervision (sterile injectable preferred).
  • Experience with SOPs, cGMP and regulatory requirements.

Responsibilities

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

Education

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

Job description

Job Description:
Job Title

Manufacturing Supervisor - Production

Business Unit

Sun Global Operations

Job Grade

G12A

Location

Pithampur

Responsibilities
Are You Ready to Create Your Own Sunshine?

At Sun Pharma, we commit to helping you "Create your own sunshine" - by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

As you enter the Sun Pharma world, you'll find yourself becoming 'Better every day' through continuous progress. Exhibit self-drive as you 'Take charge' and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we 'Thrive together' and support each other's journeys.

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

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