Sun Pharma is Hiring for Advanced R&D Roles in Baroda

Sun Pharma, a world-renowned name in the pharmaceutical industry, is expanding its Research & Development team in Baroda. We are seeking talented and experienced professionals to contribute to our cutting-edge projects.

If you are passionate about pharmaceutical sciences and want to make a significant impact, this is your opportunity to join a dynamic and innovative team.

We are looking for experts in Non-Orals, Formulation Development, and Biotechnology to fill key positions at our state-of-the-art R&D facility. This is your chance to work on challenging projects that shape the future of healthcare.

Current Openings at R&D Baroda

We have several exciting vacancies for dedicated professionals. Please review the table below for a summary of the available positions.

Function	Department	Qualification	Required Experience
MS&T – Non Orals	R&D Baroda	M. Pharm	4-7 years
Formulation Development – Non Orals	R&D Baroda	M. Pharm or PhD	5-8 years
Biotechnology – Downstream Processing	R&D Baroda	M.Sc / M.Tech / PhD	8-10 years

Key Responsibilities and Requirements

MS&T – Non Orals

As a key member of the Manufacturing, Science & Technology (MS&T) team, you will be responsible for ensuring robust and efficient manufacturing processes.

Primary Responsibilities:

• Design and implement control strategies for manufacturing processes.
• Utilize process modeling for robustness and optimization studies.
• Lead troubleshooting and investigation efforts during scale-up and execution batches (EBS).

Cross-Functional Team (CFT) Responsibilities:

• Develop and manage technology transfer documentation.
• Provide support for regulatory filings.
• Offer support to Quality Assurance (QA) and regulatory departments.
• Demonstrate a strong understanding of analytical methods.

Formulation Development – Non Orals

This role focuses on the end-to-end development of complex non-oral pharmaceutical products for regulated markets.

Required Experience:

• Extensive experience in developing non-oral products such as topical and parenteral formulations.
• Proven track record in end-to-end generic product development for ANDA filings.
• Hands-on experience with various dosage forms, including creams, ointments, gels, lotions, patches, and injectable solutions (depo, prefilled syringes, cartridges).
• Familiarity with NDA filings under 505(b)(2) and 505(b)(1) pathways is a plus.

Biotechnology – Downstream Processing

We are seeking a leader to establish and manage the downstream processing group within our Biological Drug Substance Unit.

Key Responsibilities:

• Lead the design, planning, and operation of the downstream group for both development and GMP production.
• Deliver purified recombinant proteins for clinical batches on time and within budget.
• Provide expertise in the downstream process development of large molecules, including recombinant proteins and monoclonal antibodies.
• Must possess in-depth knowledge of operating TFF and filtration systems and be proficient in interpreting experimental results using standard tools.

How to Apply

If you meet the qualifications and are ready for a new challenge, we would love to hear from you.

Please send your updated resume to: Rosemary.varghese@sunpharma.com

Join Sun Pharma and be a part of our mission to deliver high-quality, affordable medicines that improve the lives of patients worldwide. Apply now to advance your career with an industry leader