Regulatory Affairs Specialist Vacancy in Hyderabad
- Join Dr. Reddy’s as a Regulatory Affairs Specialist in Hyderabad
- Why Work with Dr Reddy’s?
- Job Overview
- Position:
- Location:
- Department:
- Experience Required:
- Employment Type:
- Key Responsibilities
- Qualifications and Skills
- Educational Background:
- Preferred Skills:
- Career Growth & Work Environment
- Apply Now
- Job Summary Table
Regulatory Affairs Specialist Vacancy in Hyderabad | M.Pharm/MSc/PhD Graduates Apply Now
Apply for the Regulatory Affairs Specialist role at Dr. Reddy’s Laboratories, Hyderabad. Open for M.Pharm, MSc, or PhD graduates with 6-12 years experience.
Join Dr. Reddy’s as a Regulatory Affairs Specialist in Hyderabad
Are you a seasoned professional with a background in M.Pharm, MSc, or PhD in life sciences or pharmaceutical sciences? Dr. Reddy’s Laboratories Limited is inviting applications for the role of Regulatory Affairs Specialist at its Hyderabad location. This is your chance to contribute to a globally respected pharmaceutical leader and join a purpose-driven team that accelerates access to affordable and innovative medicines.
Why Work with Dr Reddy’s?
Dr Reddy’s Laboratories is a leading multinational pharmaceutical company committed to innovation, access, and affordability. Operating in over 66 countries with 24,000+ employees, Dr. Reddy’s vision is rooted in sustainable development and healthcare advancement. If you’re driven by purpose and ready to make an impact, this opportunity is tailor-made for you.
Job Overview
Position:
Regulatory Affairs Specialist
Location:
Hyderabad, Telangana, India
Department:
Regulatory Affairs – IPDO (Integrated Product Development Organization)
Experience Required:
6 to 12 years
Employment Type:
Full-time, On-Premise
Key Responsibilities
- Prepare and review US ANDAs, 505(b)(2), EU and Canadian dossiers for parenteral products.
- Draft deficiency responses, regulatory strategy notes, briefing books, and ScA meeting packages.
- Coordinate with cross-functional teams, including R&D, AR&D, SCM, FTO, CTO, CMO, and CRO.
- Support commercial launch teams with document reviews and change evaluations for commercial batches.
- Ensure eCTD publication and dossier submission as per international regulatory guidelines.
- Provide regulatory input during product development and lifecycle management.
Qualifications and Skills
Educational Background:
- M.Pharm (Pharmaceutical Sciences)
- MSc (Life Sciences, Biotechnology, or related fields)
- PhD (Relevant field preferred)
Preferred Skills:
- Strong written and oral communication
- Effective team collaboration and leadership
- High adaptability and quick learning ability
- In-depth understanding of global regulatory standards
Career Growth & Work Environment
Dr. Reddy’s celebrates diversity, and every employee is nurtured for long-term growth. As an equal-opportunity employer, the company promotes a discrimination-free workplace and recognizes merit and performance.
Apply Now
Ready to step into a dynamic regulatory role? Click below to apply:Â Apply Here
Job Summary Table
| Company Name | Current Vacancies | Required Education | Experience Required |
|---|---|---|---|
| Dr. Reddy’s Laboratories | Regulatory Affairs – Parenteral | M.Pharm, MSc, PhD | 6–12 years |
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