Hetero Hiring for Regulatory Affairs Formulation (US, EU, ROW) Role

Hetero, a leading pharmaceutical company known for its innovative drug formulations and high-quality products, is hiring Regulatory Affairs professionals specializing in Formulations for US, EU, and ROW markets. This is an excellent opportunity to work with a reputed organization that emphasizes research, innovation, and global regulatory compliance.
Job Details
- Position: Regulatory Affairs – Formulation (US, EU, ROW)
- Location: Jeedimetla, Hyderabad, Telangana
- Experience Required: 3 to 9 years
- Qualification: M Pharma, B Pharma, M Sc
- Work Type: Full-time
- Mode of Hiring: Walk-in Interview

Roles & Responsibilities
- Review, compile, and submit ANDAs (Abbreviated New Drug Applications) to regulatory authorities.
- Ensure life cycle management of regulatory submissions, handling post-approval and pre-approval requirements.
- Prepare and submit MAA (Marketing Authorization Applications) for EU and ROW markets.
- Manage regulatory compliance, coordinate with internal teams, and ensure timely approvals.
- Stay updated with changing regulatory guidelines in US, EU, and ROW regions.
Key Skills Required
- Strong knowledge of ANDA submission processes and dossier compilation.
- Experience in life cycle management of regulatory affairs.
- Understanding of post-approval variations and regulatory compliance.
- Proficiency in preparing and handling Marketing Authorization Applications (MAA).
- Familiarity with international regulatory requirements for the US, EU, and ROW markets.
Walk-in Interview Details
- Date: 16th February 2025 (Sunday)
- Time: 09:00 AM – 03:00 PM
- Venue: Hetero Labs Limited, Unit VII, Jeedimetla, Qutubullapur (M), Medchal District, Hyderabad, Telangana.
- Contact Email: Chandrasekhar.r@hetero.com
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