Aurobindo Pharma is hiring experienced professionals for its Regulatory Affairs team at APLR C-1, Hyderabad, with opportunities supporting both the US and European markets. The openings are focused on regulatory submissions, approvals and CMC activities, with candidates holding relevant pharmaceutical and regulatory affairs qualifications preferred.
Job Details
| Market | Role / Requirements | Experience | Qualification |
|---|---|---|---|
| US Market | RAD-US – ANDA Filing; RAD-US – SPD-Topical / Derma | 4.5–6 Years | B.Pharm / M.Pharm, specialization in Regulatory Affairs / Pharmaceutics |
| EU Market | RA_EU_Pre & Post Approvals; RA_EU_CMC (LCM) | 2–5 Years – EU-CMC Post Approvals | M.Pharm, specialization in Regulatory Affairs / Pharmaceutics / Analysis / Regulatory Affairs / Quality Assurance |
| EU Market | RA_EU_CMC-LCM | 8–12 Years | M.Pharm, specialization in Regulatory Affairs / Pharmaceutics / Analysis / Regulatory Affairs / Quality Assurance |
US Regulatory Affairs – Requirements
Candidates should have 4.5–6 years of experience in the US Regulatory Affairs market, with exposure to:
- ANDA filing
- US regulatory submissions
- SPD-Topical / Dermatology-related regulatory activities
- Regulatory documentation and submission requirements
Qualification: B.Pharm / M.Pharm
Preferred Specialization: Regulatory Affairs / Pharmaceutics
EU Regulatory Affairs – Requirements
The EU opportunities cover pre- and post-approval activities and CMC / Lifecycle Management (LCM).
Candidates with 2–5 years of experience can apply for EU-CMC post-approval activities, while professionals with 8–12 years of experience are sought for EU-CMC-LCM roles.
Qualification: M.Pharm
Preferred Specializations:
- Regulatory Affairs
- Pharmaceutics
- Analysis
- Quality Assurance
Job Location
APLR C-1, Hyderabad
How to Apply
Interested candidates can share their updated CV with the respective recruitment contacts:
US Market:
Sreeja.Yangam@aurobindo.com
EU Market:
Pooja.Uppalapati@aurobindo.com
Open Positions
- Regulatory Affairs – US Market: 4.5–6 Years
- Regulatory Affairs – EU CMC Post Approvals: 2–5 Years
- Regulatory Affairs – EU CMC-LCM: 8–12 Years
Work Location: APLRC-1, Hyderabad.
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