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.”
Key responsibilities:
- Manage Change Control, CAPA, Market Complaints, planned/unplanned deviations, incidents, and self‑inspections through the QMS software.
- Review, prepare, and manage packing-related documentation including SOPs, BPRs, BOMs, qualification and validation protocols/reports, investigations, and market complaints.
- Prepare and execute qualification documents (URS, FAT, SAT, IQ, OQ, PQ) for packing equipment and systems.
- Execute and support packing activities related to PPV protocols.
- Prepare and manage risk assessment documents for packing processes.
- Perform EDMS activities and maintain online cGMP records.
- Ensure proper status labeling, segregation, and storage of packed materials as per defined conditions, and maintain required records.
- Conduct incident investigations and ensure timely closure.
- Coordinate with Production, Engineering, QA, QC, Warehouse, and other support departments for packing-related quality activities.
- Support project-related activities involving packing lines or equipment.
- Ensure fulfillment and timely closure of QA and internal audit observations.
