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Salary
≈ $17k – $40k per year (Estimated)
Location
In office (India)
Seniority
Middle · 4+ years exp

Confirmed on the employer's own hiring board on Oct 18, 2026. First seen by Alion on Sep 22, 2026.

Overview
Company
Impact
Profile match
Headquartered in Mumbai, India, Sun Pharmaceutical Industries Limited (Sun Pharma) is a global specialty generic pharmaceutical enterprise and the largest pharmaceutical company in India. The company manufactures and markets a broad portfolio of generic and branded generic pharmaceuticals, complex drug formulations, over-the-counter (OTC) products, and active pharmaceutical ingredients (APIs) across key therapeutic areas such as dermatology, ophthalmology, psychiatry, cardiology, and oncology. Supported by an extensive global manufacturing footprint and robust R&D capabilities, it delivers high-barrier-to-entry and affordable medicines to healthcare systems in more than 100 countries worldwide.

Job Title:

Executive - Regulatory Affairs

Business Unit:

R&D1 Regulatory Affairs

Job Grade

G12A

Location:

Panoli

At Sun Pharma, we commit to helping you “Create your own sunshine”- by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

Job Description:

  • To review and maintain GMP documents.
  • To co-ordinate QMS related activities like Change Control etc.
  • Approval of documents like SOP’s, STP’s etc.
  • To Review, follow up and compilation of data for submission of USDMF, CEP, DCP, CP, MRP for New DMF submission and DMF-Amendment / Update based on the Planning to Corporate RA, Mumbai.
  • To Review, follow up and compilation of data for submission of USDMF, DMF-Amendment / Update based on the Planning to Corporate RA, Gurgaon.
  • To Review, follow up and compilation of data for submission of Japan, China, TGA, Canadian... for New DMF submission and DMF-Amendment / Update based on the Planning to Corporate RA, Mumbai. Compilation of raw data for Registration /re-registration and queries received from authorities for ROW market, such as China, Korea, Taiwan, Indonesia, South Africa...etc.
  • To co-ordinate and organization of plant regulatory team for planning and execution of work based on the time line

Travel Estimate

NA

Job Requirements

Educational Qualification

M.Pharm/M.Sc

Experience

4-6 years of relevant experience

Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

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