🚀 Aurobindo Pharma Hiring 2026 | Regulatory Affairs (US & EU Markets) | Hyderabad
Aurobindo Pharma Limited is hiring experienced Regulatory Affairs Professionals for its US & EU Markets team at APLRC1, Hyderabad. This is an excellent opportunity for candidates with regulatory submission experience looking to build a career with a leading global pharmaceutical company.
📌 Job Details
🏢 Company: Aurobindo Pharma Limited
💼 Job Role: Regulatory Affairs Professional (US & EU Markets)
📍 Work Location: APLRC1, Hyderabad
📄 Employment Type: Fixed-Term Contract
🎓 Qualification
- M.Pharm
- B.Pharm
- M.Sc
💼 Experience Required
- 2–12 Years in Regulatory Affairs
💊 Product Experience
- Oral Solid Dosages (OSD)
- Injectables
- Biologics / Biosimilars
- Oncology Products
📋 Key Responsibilities
✅ Handle US Regulatory Submissions (ANDA, NDA & 505(b)(2))
✅ Manage EU Registrations (Centralized, Decentralized, MRP & National Procedures)
✅ Prepare and submit Post-Approval Variations
✅ Perform Dossier Preparation & Review as per USFDA & EMA guidelines
✅ Manage eCTD Publishing activities
✅ Review and maintain US & EU Product Labeling
✅ Coordinate with R&D, Manufacturing and Commercial Teams
🎯 Required Skills
✔ Strong knowledge of USFDA & EMA Regulations
✔ Experience in Regulatory Submissions and Lifecycle Management
✔ Good communication and analytical skills
✔ Excellent documentation and organizational abilities
📩 How to Apply
📧 US Market: Sreeja.Yangam@aurobindo.com
📧 EU Market: Pooja.Uppalapati@aurobindo.com
Email Subject:
- 🇺🇸 Application for RA – US Market
- 🇪🇺 Application for RA – EU Market
📄 Send your updated CV with your latest experience details.
⚠ Important Notes
🔹 This position is on a Fixed-Term Contract.
🔹 Candidates who attended an Aurobindo Pharma interview within the last 6 months are not eligible for this opening.
🌟 Don’t miss this excellent opportunity to join Aurobindo Pharma and contribute to global regulatory operations for the US & EU markets! Apply today.
