M Pharm Job at Sun Pharma | Regulatory Affairs | Apply Now
In the high-stakes arena of global pharmaceuticals in 2026, the bridge between a breakthrough formulation and a patient’s access is built by regulatory experts. If you are looking for an M Pharm Job that offers exposure to the world’s most stringent markets, this Executive position at Sun Pharma’s Tandalja R&D center is your premier choice. As the pharmaceutical landscape becomes increasingly complex, this Regulatory Affairs Job provides a unique platform to manage the lifecycle of life-saving medicines across the US, EU, and beyond.
- Job Position: Executive – Regulatory Affairs
- Location: Tandalja – R&D
About the Company
Sun Pharmaceutical Industries Ltd is the fourth-largest specialty generic pharmaceutical company in the world and the number one provider in India. With a global footprint spanning over 100 countries, a Sun Pharma career offers the opportunity to work within a highly integrated network of manufacturing sites and R&D centers. The company’s philosophy, “Create your own sunshine,” emphasizes self-drive, collaborative spirit, and continuous progress. For those seeking a Sun Pharma career, the Baroda (Vadodara) facility stands as a strategic hub for innovation, where regulatory professionals ensure that every product meets the gold standard of global compliance.
Key Responsibilities: Navigating this Regulatory Affairs Job
As an Executive in Regulatory Affairs, your role is pivotal to the company’s business continuity. You are not just managing paperwork; you are ensuring that dossiers for markets like the US, EU, Australia, Canada, and Israel (IL) are scientifically sound and audit-ready. This is a high-impact Regulatory Affairs Job where your technical review directly influences the speed of drug launches.
- Dossier Mastery: Compile and review dossiers (CTD/eCTD) for both solid oral and non-oral dosage forms for top-tier international markets.
- Query Resolution: Lead the review and compilation of query responses, ensuring that the concerns of health authorities like the FDA or EMA are addressed with scientific precision.
- Lifecycle Management: Oversee the post-approval lifecycle, managing variations and renewals to ensure continuous market presence—a critical component of this Regulatory Affairs Job.
- Stakeholder Synergy: Review all documents received from cross-functional stakeholders to ensure data integrity during dossier compilation.
- Team Leadership: Allocate projects to regulatory associates and manage the workflow to meet strict submission timelines.
- Strategic Liaison: Act as the single point of contact for all regulatory activities pertaining to the Israel and Palestine markets.
Requirements for this M Pharm Job
Sun Pharma is seeking a dynamic professional who thrives in a detail-oriented environment. This M Pharm Job is specifically designed for candidates who have moved past the entry-level phase and are ready for more complex responsibilities.
- Educational Qualification: You must hold an M.Pharm degree. This ensures you have the deep pharmaceutical knowledge required to review complex dosage form data.
- Experience: A tenure of 2 – 4 years in regulatory affairs is essential.
- Technical Knowledge: A strong understanding of the regulatory requirements for US, EU, and Canada markets is highly preferred.
- Analytical Skills: You must be able to review raw data and query responses to identify discrepancies before submission.
In summary, the Executive role in Regulatory and Business Continuity is a definitive M Pharm Job for those ready to lead in the R&D space. By embarking on a Sun Pharma career in 2026, you position yourself at the heart of one of the world’s most successful pharmaceutical giants. This Regulatory Affairs Job offers the perfect blend of technical rigor and project management, ensuring that your professional growth remains “better every day.” If you are a detail-oriented M.Pharm professional with a proactive problem-solving mindset, Sun Pharma’s Baroda R&D center is the ideal place to create your own sunshine.
