Hetero Pharma Hiring: Regulatory Affairs (RA) Specialist – Apply Now
About Hetero Pharma
Hetero is a leading global pharmaceutical company and the world’s largest manufacturer of anti-retroviral drugs. With over 25 years of expertise, Hetero operates across APIs, generics, biosimilars, branded generics, and custom pharma services.
The company runs 36 world-class manufacturing facilities approved by major global regulatory authorities and has a diverse portfolio of 300+ products across key therapeutic areas including HIV/AIDS, Oncology, Cardiology, Neurology, Diabetes, Hepatology, Nephrology, Urology, Immunology and more.
Hetero maintains a strong global footprint across 145+ countries, committed to providing high-quality, affordable healthcare solutions worldwide.
Vacancy Details – RA Specialist (Formulations)
Position: Regulatory Affairs Specialist
Markets: ROW, EU, US
Location: Jeedimetla, Hyderabad
Job Responsibilities
- Preparation, review, and submission of regulatory dossiers
- Strong hands-on experience in Life Cycle Management (LCM)
- Managing pre-approval and post-approval regulatory activities
- Good knowledge of MAA (Marketing Authorization Application)
- Experience in CMC (Chemistry, Manufacturing & Controls)
Eligibility Criteria
- Qualification: M Pharma / B Pharma / M.Sc
- Experience Required: 3 to 9 Years
How to Apply?
Interested candidates can email their updated CV to:
chandrasekhar.r@hetero.com
Subject Line: Application for RA Specialist – Hetero Pharma
For more details, visit: www.hetero.com
