Opportunity for B.Pharm, MSc as Senior Executive / Manager at Sun Pharma

Sun Pharma is India’s No. 1 pharmaceutical company and a leading global player in specialty medicines. With over 40 manufacturing facilities and a diverse portfolio, we deliver high-quality medicines across 100 countries. Driven by a commitment to innovation, we continuously strive to enhance access to medicines and improve patient care, creating better health outcomes for millions around the world.

Post : Senior Executive / Manager - Corporate Quality Compliance

Job Description
1. Maintain a comprehensive database of regulatory inspections conducted across Sun Pharma sites.
2. Assess regulatory inspection citations from internal sites to identify and implement global corrective and preventive actions.
3. Evaluate internal learnings such as Quality Alerts and consultant observations to derive global actions.
4. Analyse FDA enforcement actions (e.g., Form 483s, Warning Letters issued to other organizations) to proactively identify risks and define global actions.
5. Develop and implement global actions, including:
• Reviewing relevant regulatory guidance
• Assessing current site practices
• Drafting global action recommendations
• Preparing reference procedures and formats for implementation
• Finalizing recommendations in consultation with the Global Action Committee and stakeholders
• Issuing and approving global actions in TrackWise

6. Coordinate with manufacturing sites to ensure effective implementation of global action recommendations.
7. Review site-level action closures for completeness and accuracy.
8. Ensure closure of global actions once all associated site action records are completed.
9. Communicate global action status to relevant stakeholders regularly.
10. Share internal and external learnings across the organization to promote continuous improvement.
11. Review draft responses to regulatory inspection observations for quality and compliance, as needed.
12. Maintain and analyse inspection observation trends across sites to identify improvement opportunities.
13. Perform additional duties as assigned by the Head of Corporate Quality Compliance and CQA.
14. Hands on experience in Trackwise, EDMS and Microsoft Excel, Pivot, etc.

Additional Information
Experience : 10+ Yrs
Qualification : M.Sc / B.Pharm
Location : Tandalja - R&D
Industry Type : Pharma/ Healthcare/ Clinical research
Business Unit : Corporate Quality Compliance
End Date : 20th October 2025