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Aurobindo Pharma, a global leader in pharmaceutical innovation, is expanding its Regulatory Affairs team! We are looking for skilled and driven professionals to support our growing portfolio of EU market submissions. If you have a passion for regulatory science and a strong background in formulation R&D, this is your chance to shine!
Exciting Career Opportunity at Aurobindo Pharma – We’re Hiring! 🚀
Position Overview:
Position: Regulatory Affairs Professionals (Formulation R&D) – EU Markets
Location: Hyderabad
Are you passionate about regulatory science and formulation R&D? Join Aurobindo’s dynamic Regulatory Affairs team and play a pivotal role in supporting our global market submissions, especially in the EU region.
Who We’re Looking For:
Educational Qualification: M. Pharm in Pharmaceutics or Pharmaceutical Analysis
Experience: 3–6 years in FRD/FARD/QA with minimum 1 year of Regulatory Affairs experience in the EU market
Current Openings:
• EU Regulatory Affairs – Hands-on experience with Module 2 & 3 is essential
Key Responsibilities:
1. Prepare and review technical documents for EU filing requirements (Modules 2 & 3 – Quality Module)
2. Interpret and implement EU regulatory guidelines (ICH, EMA)
3. Manage post-approval variations in EU markets
4. Review plant-related documents with a basic understanding of QA
Apply Now!
Send your updated resume to:
📧 Pooja.Uppalapati@aurobindo.com
Subject Line: “Application for EU Market”
