About Company:
Hetero is one of India’s leading generic pharmaceutical companies and the world’s largest producer of anti-retroviral drugs. Backed by 25 years of expertise in the pharmaceutical industry, Hetero’s strategic business areas spread across APIs, generics, biosimilars, custom pharmaceutical services and branded generics. The company is globally recognized for its strengths in Research and Development, manufacturing and commercialization of a wide range of products. Hetero has 36 state-of-the-art manufacturing facilities strategically located worldwide, approved by stringent global regulatory authorities. Our portfolio includes 300 plus products encompassing major therapeutic categories such as HIV/AIDS, Oncology, Cardiovascular, Neurology, Hepatitis, Nephrology, Urology, Diabetes, Ophthalmology, Hepatology and Immunology etc. Hetero has a strong global presence in over 145+ countries and focusses on making affordable medicines accessible to patients worldwide.
Vacancy Details:
Job Description:
Exciting Career Opportunity at HETERO! 🌟
We are looking for passionate and skilled professionals to join us as a Regulatory Affairs Specialist in formulations
📍 Location: Jeedimetla, Hyderabad
🌎 Markets: Formulation (ROW, EU, US)
What You’ll Do:
✅ Prepare, review, and submit dossiers
✅ Drive Life Cycle Management activities
✅ Manage Pre & Post-approval processes
✅ Work on MAA (Marketing Authorization Applications)
✅ Gain strong exposure in CMC
What We’re Looking For:
🎓 Qualification: M. Pharma / B. Pharma / M. Sc
💼 Experience: 3–9 years
If you’re ready to grow your career with one of the fastest-growing pharmaceutical companies, we’d love to hear from you! 🙌
How to Apply?
📩 Share your CVs at chandrasekhar.r@hetero.com with the subject line:
“Application for RA”
Know someone who fits this role? Feel free to refer and share!-let’s help great talent find great opportunities!
Let’s build a healthier future together!
