M Pharma Jobs: Sun Pharma is Hiring an Executive – Regulatory Affairs and Business Continuity – Apply Now
Are you planning to establish your career in pharmaceutical industry but couldn’t find M Pharma Jobs? Sun Pharma is Hiring for the role of Executive – Regulatory Affairs and Business Continuity at its Baroda R&D location. This role offers an exciting opportunity to contribute to global drug development, manage regulatory submissions, and ensure compliance with international standards. If you are a passionate professional with an M. Pharm degree, Sun Pharma provides the perfect platform to grow, lead, and create your own sunshine.
About the Company
Sun Pharmaceutical Industries Ltd is the world’s fourth-largest specialty generic pharmaceutical company and India’s largest pharmaceutical company, trusted by millions of patients across more than 100 countries. Founded in 1983, Sun Pharma delivers high-quality, affordable medicines in over 40 therapeutic areas, including cardiology, psychiatry, neurology, gastroenterology, and diabetology. Headquartered in Mumbai, Sun Pharma operates with a strong commitment to innovation, regulatory compliance, and global quality standards. Its R&D-driven approach and extensive manufacturing network have made it a leader in both branded and generic formulations. With a mission to improve patient lives worldwide, Sun Pharma continues to create sustainable healthcare solutions and empower professionals to grow and lead in the pharmaceutical industry.
Job Details:
- Job Title: Executive – Regulatory Affairs and Business Continuity
- Location: Baroda, Tandalja – R&D
- Company: Sun Pharmaceutical Industries Ltd
Job Summary:
- New Submissions: Collaborate with product development and cross-functional teams to ensure regulatory compliance during drug product design and development. Provide input on filing strategies, review documents, and prepare high-quality dossiers for faster approvals.
- Approvals: Prepare and submit timely responses to regulatory deficiencies to enable swift product approvals.
- Lifecycle Management: Manage regulatory compliance for approved products, including annual reports, renewals, and submission of variations or supplements. Ensure implementation of regulatory decisions and maintain a central repository of product information.
- Self-Development: Stay updated with evolving regulatory guidelines, deliver presentations, and contribute to knowledge sharing.
Requirements:
- Education: M. Pharm
- Experience: 2–5 years in regulatory affairs
- Skills: Strong understanding of regulatory guidelines, dossier preparation, compliance, and lifecycle management.
