Sun Pharma, the fourth-largest specialty generic pharmaceutical company in the world, is committed to delivering high-quality and affordable medicines trusted by healthcare professionals and patients across more than 150 countries. As India’s largest and most valuable pharmaceutical company by market capitalization, we continue to grow and are seeking motivated professionals to join our dynamic team.
Currently, we have exciting opportunities in Regulatory Affairs – Formulation at our Vadodara location. This is your chance to contribute to global health, gain exposure in international markets, and grow your career with one of the most trusted names in pharmaceuticals.
Walk-In Interview Details
Date: 25 August
Time: 9:30 AM – 1:30 PM
Venue: Sun Pharmaceutical Industries Ltd, Near Akshar Chowk, Sun Pharma Road, Tandalja, Baroda 390012
If you’re looking to grow your career in Regulatory Affairs, join us for a walk-in interview.
Job Overview
Position: Regulatory Affairs – Formulation
Qualification: M.Pharm
Experience: 2 to 6+ years
Job Location: Vadodara
Openings: 05 Positions
Key Responsibilities
- Data and Document Review: Perform in-depth reviews of all data and documents related to product registrations, ensuring compliance with various health authorities (experience with non-oral formulations is preferred).
- Registration Dossiers Compilation: Compile registration dossiers for submission to health authorities in regions including the US, Canada, Europe, and Australia.
- Response Preparation: Address and respond to deficiency letters received from health agencies, ensuring timely and compliant responses.
- Lifecycle Management: Maintain and manage life-cycle activities and post-approval changes for drug product registration dossiers.
- Cross-Functional Support: Provide regulatory guidance and support to various internal departments such as quality assurance, manufacturing, and product development.
- Scientific Advice Submission: Prepare and submit scientific advice applications to health authorities to facilitate approvals and product registrations.
- eCTD Submission: Compile, verify, and submit dossiers in electronic Common Technical Document (eCTD) format through electronic gateways.
Skills Required
- Strong understanding of regulatory guidelines and requirements across major markets.
- Experience in dossier preparation and lifecycle management.
- Knowledge of eCTD compilation and submission.
- Ability to work cross-functionally and provide regulatory guidance.
- Excellent communication skills, both written and verbal.
Why Join Sun Pharma?
At Sun Pharma, we believe in fostering a culture of innovation, collaboration, and growth. As part of the Regulatory Affairs team, you’ll work on global submissions, deal with international agencies, and have the chance to make a meaningful impact on global health. Our commitment to quality and innovation has made us a trusted leader in pharmaceuticals worldwide.
Learn more about Sun Pharmaceutical Industries on Wikipedia.
Interview Venue Details
Address:
Sun Pharmaceutical Industries Ltd, Near Akshar Chowk, Sun Pharma Road, Tandalja, Baroda 390012
Google Maps Location: Sun Pharma Tandalja
Application Instructions
For those who are unable to attend the walk-in interview, you can still apply by sending your resume to:
Email: Hr.tandalja@sunpharma.com
We look forward to seeing you at the interview or receiving your application via email!
Why Work in Regulatory Affairs at Sun Pharma?
Working in Regulatory Affairs at Sun Pharma offers opportunities to contribute to life-saving medicines, engage with global health authorities, and develop expertise in international regulatory environments. Our team is instrumental in ensuring our products meet stringent quality and regulatory standards, helping us maintain our position as a global leader in pharmaceuticals. Join us and be part of a company that’s shaping the future of healthcare.
Walk-In Interview Preparation
To make the most of your interview opportunity, we recommend:
- Bringing Multiple Copies of Your Resume: Ensure your resume highlights your regulatory experience, technical skills, and relevant qualifications.
- Research: Familiarize yourself with Sun Pharma’s global operations and our focus on specialty generics.
- Be Ready to Discuss: Your experience with regulatory submissions, dossier compilation, and response preparation for various international markets.
This is an exciting opportunity to advance your career with a globally recognized pharmaceutical leader. We hope to meet talented individuals who are ready to contribute to the world of healthcare.
Join the Sun Pharma Family
Sun Pharma is a global leader with a commitment to innovation, excellence, and patient care. We offer a rewarding work environment where you can develop your career and make an impact on global health. If you’re passionate about making a difference in the pharmaceutical industry, this is the place for you.
