Explore Top Regulatory Affairs Jobs at Sun Pharma | Apply Today
Looking for rewarding Regulatory Affairs Jobs in the pharmaceutical industry? Sun Pharmaceutical Industries Ltd, one of India’s top global pharma companies, is now hiring for the Sr. Executive – Regulatory Affairs (RA) position at its Tandalja R&D Centre, Baroda. This is an excellent opportunity for talented M Pharm professionals eager to advance their careers through impactful Sun Pharma Jobs. Join a workplace that encourages growth, innovation, and collaboration where you truly can “Create Your Own Sunshine.” Find out more about the regulatory affairs roles they offer.
Job Details
- Job Title: Executive- Regulatory & Business Continuity
- Location: Tandalja – R&D
- Company: Sun Pharmaceutical Industries Ltd
- Business Unit: R&D1 Regulatory Affairs
- Job Grade: G12A
- Location: Baroda. This is a prime location for regulatory affairs careers.
About the Company
Sun Pharmaceutical Industries Ltd is a global leader in specialty generics and healthcare innovation. The company provides professionals with opportunities to excel in Regulatory Affairs Jobs, research, and manufacturing. At Sun Pharma, M Pharm graduates can build successful careers while contributing to global health advancements. The organization’s culture promotes growth, leadership, and the spirit to “Create Your Own Sunshine.” There’s a lot to gain from the regulatory affairs jobs offered here.
Job Description For Regulatory Affairs Jobs at Sun Pharma
- Develop and implement registration strategies for Brazil submissions.
- Understand authority guidance and manage filing of new products and post-approval changes.
- Review documents related to product registration and dossier submissions to enable faster approvals.
- Prepare responses to deficiency letters from Anvisa, Brazil. This important task is part of regulatory affairs jobs.
- Maintain life-cycle (PCH) and post-approval changes for drug product registration dossiers, ensuring timely approval circulation.
- Provide regulatory support to cross-functional teams.
- Assess change controls per regulatory guidelines.
- Prepare and submit scientific advice to Anvisa, Brazil.
Key Responsibilities | Sun Pharma Jobs
- Strategize and manage regulatory submissions for international markets.
- Support cross-functional regulatory operations for compliance.
- Lead documentation review and lifecycle management for faster product approvals, essential for regulatory affairs.
- Ensure regulatory excellence and alignment with global standards.
Qualifications For Regulatory Affairs Job
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Educational Qualification: M Pharm (Master of Pharmacy)
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Experience: 3–5 years in Regulatory Affairs
Why Join This Company?
At Sun Pharma, your career growth and well-being come first. The company empowers you to take charge of your journey, grow continuously, and thrive together in a collaborative community. As part of the global Sun Pharma Jobs network, you’ll make a meaningful impact while building expertise in Regulatory Affairs—a perfect fit for ambitious M Pharm candidates. Indeed, many are finding rewarding regulatory affairs jobs here.
