📢 Aurobindo Pharma Hiring: Regulatory Affairs Jobs for US & EU Markets | Hyderabad | 2-12 Years Exp | Apply Now 📢
Aurobindo Pharma Regulatory Affairs Jobs 2026: Aurobindo Pharma is hiring experienced professionals for Regulatory Affairs roles focused on US and EU markets at its Hyderabad facility – APLRC-1. Ideal for candidates with ANDA filing, Post-approval, LCM, and CMC experience. Experience: 2-12 Years.
📋 About the Company
Aurobindo Pharma is a global pharmaceutical leader known for high-quality generic medicines, APIs, and formulations. With a strong commitment to innovation, regulatory excellence, and affordable healthcare, Aurobindo serves markets worldwide from advanced manufacturing facilities.
📋 Job Details
| Company Name | Aurobindo Pharma |
| Department | Regulatory Affairs – US & EU Markets |
| Experience | 2 – 12 Years, varies by role |
| Qualification | B.Pharm / M.Pharm – Regulatory Affairs/Pharmaceutics/Analysis/QA preferred |
| Location | Hyderabad – APLRC-1 |
| Work Type | On-site |
📋 Available Positions
1. RAD-US – ANDA Filing / Post Approvals LCM / SPD-Topical-Derma
- ✔ Department: Regulatory Affairs – US
- ✔ Experience: 4.5 – 6 Years
- ✔ Qualification: B.Pharm / M.Pharm
2. RA-EU – Pre & Post Approvals / CMC LCM
- ✔ Department: Regulatory Affairs – EU
- ✔ Experience: 2 – 5 Years for Pre & Post | 8 – 12 Years for CMC LCM
- ✔ Qualification: M.Pharm
✅ Skills & Qualifications Required
- ✔ Hands-on experience in US/EU regulatory filings and post-approvals
- ✔ Strong knowledge of ANDA, LCM, and CMC requirements
- ✔ Expertise in topical/derma formulations – preferred for US SPD
- ✔ Excellent documentation and communication skills
- ✔ Understanding of global regulatory guidelines
📋 Key Responsibilities
- ✔ Prepare and review regulatory submissions for US/EU
- ✔ Manage post-approval changes and life cycle management
- ✔ Coordinate with cross-functional teams for filings
- ✔ Handle CMC documentation and updates
- ✔ Respond to regulatory queries and ensure compliance
🎁 Benefits & Perks
- ✔ Career growth in a global pharma leader
- ✔ Opportunities for international regulatory exposure
- ✔ Competitive compensation and benefits
- ✔ Collaborative and innovative work culture
- ✔ Professional development in regulatory affairs
📝 How to Apply
Interested candidates can apply via email. Mention the specific role in the subject line.
| For US Market | us.ra@aurobindo.com |
| For EU Market | eu.ra@aurobindo.com |
Note: Walk-in interview not applicable. Apply via email only.
❓ FAQs
Q1: What experience is needed for US Regulatory roles?
Q2: What are the EU experience requirements?
Q3: Where is the work location?
Q4: Which qualifications are preferred?
🔗 Important Links
Company Website: www.aurobindo.com
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⚠️ Note: Eligible candidates with US/EU regulatory experience should apply immediately via email. This is an excellent opportunity for senior pharmaceutical careers in Regulatory Affairs.