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:
- Lead and manage overall production operations to ensure timely execution of commercial, exhibit, scale-up, pre-validation, validation, and process validation batches as per approved production schedules.
- Monitor daily production planning, line scheduling, and review Plan vs. Actual performance to achieve business targets.
- Ensure optimum utilization of manpower, equipment, utilities, materials, and manufacturing areas to maximize productivity and efficiency.
- Coordinate with cross-functional teams to ensure uninterrupted manufacturing activities and timely batch completion.
- Ensure products are manufactured, packaged, and stored in compliance with approved procedures, specifications, and current Good Manufacturing Practices (cGMP).
- Drive Quality Systems implementation, including Deviations, Change Controls, CAPAs, Investigations, Risk Assessments, Market Complaints and Global Actions.
- Review and approve SOPs, Master Batch Records, validation protocols/reports, specifications, risk assessments, and other GMP documents.
- Ensure production records and batch documentation are reviewed, completed, and approved in accordance with established procedures.
- Maintain a constant state of Inspection Readiness for regulatory inspections and customer audits.
- Ensure implementation and compliance with ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available).
- Lead and monitor Data Integrity programs across production systems and processes.
- Review and approve Audit Trail Reviews (ATR) for GMP-critical computerized systems and electronic records.
- Collaborate with Engineering and Automation teams for equipment upgrades, digitalization initiatives, and system automation projects.
- Ensure manufacturing systems and computerized systems remain validated and compliant throughout their lifecycle.
- Ensure full compliance with Environment, Health, Safety (EHS), and organizational safety standards.
- Maintain high standards of discipline, employee engagement, and team morale.
