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.
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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.
Travel Estimate
Job Requirements
Educational Qualification
B. Pharma/M. Pharma
Experience
Tenure: 15-18 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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