Aurobindo Pharma, one of Indiaโs leading pharmaceutical companies, is inviting applications for Regulatory Affairs (RA) vacancies at its APLRC1 facility in Bachupally, Hyderabad. This opportunity is ideal for M.Pharm (Pharmacology) freshers and experienced RA professionals with hands-on exposure to Module 1 (M1) for EU and Canada.
If you’re looking to build a strong career in Regulatory Affairs, this is one of the best openings to apply for in 2025.
๐ Job Summary
- Role: Regulatory Affairs
- Experience: 0โ3 Years
- Qualification: M.Pharm (Pharmacology)
- Location: APLRC1, Bachupally, Hyderabad
- Industry: Pharmaceuticals
- Company: Aurobindo Pharma
โจ Responsibilities
- Prepare, review, and compile regulatory submissions for EU and Canada markets
- Manage and update Module 1 (M1) documentation
- Ensure compliance with global regulatory guidelines and internal SOPs
- Coordinate with cross-functional teams including QC, QA, and R&D
- Support lifecycle management of regulatory dossiers
- Track regulatory updates and ensure timely submission activities
๐ Required Qualifications
- M.Pharm in Pharmacology (Freshers encouraged to apply)
- 0โ3 years of experience in Regulatory Affairs
- Preferred experience in:
- EU/Canada submissions
- M1 document preparation and review
- Strong knowledge of regulatory guidelines and dossier requirements
- Excellent communication and documentation skills
๐ผ Benefits of Working at Aurobindo Pharma
- Opportunity to grow in a top global pharmaceutical company
- Exposure to international regulatory submissions
- Supportive work environment & learning-focused culture
- Competitive salary and benefits package
๐ฉ How to Apply
Interested and eligible candidates can apply by sharing their updated CV to:
๐ง Email: Sreeja.Yangam@aurobindo.com