Eugia Pharma Specialities Ltd (Aurobindo Pharma group) is conducting a mega walk-in interview on Sunday, 23rd November 2025 in Hyderabad for experienced Regulatory Affairs professionals. If you have 3–10 years of experience in CMC Regulatory Affairs or Post-Approval Labeling (US, EU, ROW, Canada), this is your chance to join one of India’s fastest-growing injectable and complex generics companies.
Walk-In Interview Details – Regulatory Affairs (CMC & Labeling)
- Date: 23rd November 2025 (Sunday)
- Time: 9:00 AM to 11:00 AM
- Venue: Aurobindo Pharma Ltd., Research Centre-I, Survey No. 313, Bachupally, Hyderabad, Telangana – 500090
- Contact Persons: Reshma / Shaher Banu
- Email (for those who can’t attend):Shaher.Banu@eugiapharma.com
Documents to Carry: Updated resume, educational certificates, PAN card, Aadhaar card, recent increment letter, and payslips of last 3 months.
Open Positions & Eligibility
| Designation | Experience | Qualification | Key Skills / Role |
|---|---|---|---|
| Senior Executive | 3–6 years | B.Pharm / M.Pharm | CMC Dossiers, Post-Approval Labeling (US/EU/CA/ROW) |
| Assistant Manager | 6–8 years | M.Pharm preferred | Variation Management, Lifecycle Management |
| Deputy Manager | 8–10 years | M.Pharm | Team handling, Agency interaction, Complex submissions |
Primary Markets: United States, Europe, Canada, Rest of World (ROW)
Key Responsibilities
- Preparation and submission of high-quality CMC dossiers (Module 3) for ANDA/NDA/MAA
- Handling post-approval changes (PAS, CBE-30, Annual Reports) and labeling updates
- Regulatory strategy for lifecycle management of injectable and complex products
- Interaction with global regulatory agencies (USFDA, EMA, Health Canada, etc.)
- Ensuring compliance with current ICH, USFDA, EU, and other regional guidelines
Required Qualifications & Skills
- B.Pharm / M.Pharm from a recognized university
- 3–10 years of hands-on experience in Regulatory Affairs – CMC or Post-Approval Labeling
- Excellent knowledge of eCTD structure and publishing tools (Lorenz, Docubridge, etc.)
- Strong communication and documentation skills
- Immediate or early joiners preferred
Why Join Eugia Pharma?
- Work on cutting-edge sterile injectables and oncology portfolio
- Fast-track career growth in a USFDA & EU-approved facility
- Competitive salary, performance incentives, and best-in-class benefits
- Global exposure with direct interaction with US/EU/CA regulatory teams
How to Apply
- Attend the walk-in on 23rd Nov 2025 (9–11 AM) at Bachupally, Hyderabad
- Or email your updated resume to Shaher.Banu@eugiapharma.com with subject: “Regulatory Affairs – [Your Designation] – [Years of Exp]”
Frequently Asked Questions (FAQs)
1. Can freshers apply for these Regulatory Affairs roles at Eugia? No, these positions require minimum 3 years and up to 10 years of relevant experience in CMC or Post-Approval Labeling.
2. Is the venue at Pashamylaram or Bachupally? The walk-in is being conducted at Aurobindo Pharma Research Centre-I, Bachupally (near Pashamylaram), Hyderabad.
