MPharma Vacancies Latest at Sun Pharma – Apply Now
Sun Pharmaceutical Industries Ltd, India’s leading pharmaceutical company, is hiring for the position of Executive – Regulatory and Business Continuity at its R&D center in Baroda. This exciting opportunity enables skilled professionals to contribute to global drug development, regulatory submissions, and lifecycle management, while advancing their careers with one of the most respected names in the pharmaceutical industry.
- Job Role: Executive – Regulatory and Business Continuity
- Business Unit: R&D1 Regulatory Affairs
- Job Grade: G12A
- Job Location: Baroda, Gujarat (Tandalja – R&D)
- Tenure: 2-5 years
About the Company
Sun Pharmaceutical Industries Ltd is India’s leading pharmaceutical company and the world’s fourth-largest specialty generic pharma firm. With operations in over 100 countries, Sun Pharma is dedicated to delivering high-quality, affordable medicines while promoting innovation, growth, and a positive global impact on healthcare.
Education:
Experience:
2–5 years in Regulatory Affairs or related functions.
Job Description
As an Executive in Regulatory Affairs and Business Continuity at Sun Pharma, you will be responsible for managing new submissions, regulatory approvals, and lifecycle management of approved drug products. The role requires collaboration with cross-functional teams (CFTs), preparation of high-quality dossiers, and ensuring regulatory compliance to support global product development and launches.
Key Responsibilities
New Submissions
- Work with Product Development and CFTs to include timely regulatory information.
- Provide input on document requirements and regulatory filing strategies.
- Review and approve regulatory documents.
- Prepare and submit dossiers to enable faster approvals.
- Coordinate scientific discussions and prepare meeting packages with regulatory agencies.
- Anticipate deficiencies and implement mitigation plans.
Approvals
- Prepare and submit timely responses to regulatory deficiencies to enable product approvals.
Lifecycle Management
- Ensure timely submission of annual reports and renewals.
- Evaluate, prepare, and submit variations or supplements impacting product supplies.
- Maintain compliance with regulatory decisions and change management requirements.
- Ensure product information is updated in central repositories.
Self-Development
- Stay updated on regulatory guidelines.
- Deliver presentations and contribute to knowledge-sharing sessions.
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