Executive
Actively Reviewing the ApplicationsSUN PHARMA
India, Delhi
Full-Time
On-site
INR 1–1 LPA
Posted 2 days ago
•
Apply by June 16, 2026
Job Description
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.
Are You Ready to Create Your Own Sunshine?
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.”
Qualification: B.Pharma
Experience: 5+ years
Job Responsibilities
Are You Ready to Create Your Own Sunshine?
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.”
Qualification: B.Pharma
Experience: 5+ years
Job Responsibilities
- Authorized to sign as a doer and verifier in:
- Batch Manufacturing Record, BMR Requisition, BMR Issuance Logbook.
- Protocols, Risk Assessment.
- Authorized to sign as a checker/verifier in following document,
- Finished product logbook etc.
- To prepare new BMR, revise BMRs within time.
- To assist in preparation of Change Control, Corrective Action Plan & New Equipment’s preparation.
- Handling of corrective and preventive action.
- To ensure the compliance of various in-process control instructions provided in BMR, MBMR.
- Preparation and updation of SOPs, BMRs, Log books, protocols and compliance thereof with training of people on the same.
- Handling and monitoring of Environmental monitoring system (EMS) system.
- To maintain daily production report, machine utilization on day to day basis.
- To learn EMS, review the report on daily basis. (Action, alert limit, breakdown maintenance).
- Training to all technician & supervisor for new BMRs and revised BMRs to comply with the GMP.
- To prepare process performance qualification/process validation protocols, study protocols.
- To prepare failure mode effect analysis, risk assessment for product/process.
- To undergo functional training, cGMP training or any other training identified as per schedule.
- Any other responsibility assigned by department head after ensuring the relevant training status.
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