Location: India
Experience: 2 – 10 Years
Qualification: M.Pharm / B.Pharm
Job Type: Full-Time | Verified Job
Published Date: May 5, 2025
Hiring Mode: Email Application
✨ Company Overview
Aurobindo Pharma Ltd. is one of India’s most renowned multinational pharmaceutical giants. With a presence in over 155 countries, it is currently the 2nd largest generic medicine provider in the USA and a top 10 player across major European markets like Germany, France, the UK, and Portugal.
If you’re a pharmaceutical professional looking to build a serious, global-impacting career, Aurobindo Pharma is hiring now for multiple roles in their Regulatory Affairs and Formulation R&D (FR&D) departments.
🔍 Open Positions Breakdown
1️⃣ Regulatory Affairs Associate – EU Regulatory Team (OSD)
- Experience Required: 2–10 Years
- Qualification: M.Pharmacy
- Key Role:
You will handle EU regulatory submissions for Oral Solid Dosage (OSD) products. Expect responsibilities like compiling regulatory documents, ensuring EU compliance, and coordinating with regulatory bodies.
2️⃣ Regulatory Affairs Associate – US & Canada Team (Injectable)
- Experience Required: 2–10 Years
- Qualification: M.Pharmacy
- Key Role:
Manage injectable product submissions in the US and Canada. Tasks include lifecycle management of regulatory documentation and strict adherence to US FDA standards.
3️⃣ FR&D – OSD Cost Improvement Projects
- Experience Required: 2–6 Years
- Qualification: M.Pharmacy
- Key Role:
Join the Formulation Research & Development team to lead cost reduction strategies for OSD formulations, without compromising on efficacy or compliance.
4️⃣ Regulatory Affairs Reviewer – CMC-SPD (US)
- Experience Required: 2–6 Years
- Qualification: M.Pharm / B.Pharm
- Key Role:
Review Chemistry, Manufacturing, and Controls (CMC) documents and Standard Procedures Documents (SPD) for US regulatory submissions. Prior US regulatory experience is preferred.
🧠 What Makes You a Great Fit?
Aurobindo Pharma is looking for dedicated professionals with a sharp mind and strong collaborative skills. Ideal candidates will bring:
- ✔️ Excellent knowledge of regulatory submission processes
- ✔️ Good grasp of GMP and FDA regulations
- ✔️ Skills in data analysis and documentation review
- ✔️ Ability to work with cross-functional teams
- ✔️ Proficiency in regulatory software tools
- ✔️ Strong written & verbal communication
📸 In-Blog Image
Image Description:
“The FR&D team at Aurobindo Pharma focuses on cost-effective, compliant pharmaceutical innovations for global markets.”
📋 Application Process
📱 How to Apply:
Submit your latest resume highlighting relevant qualifications and experience via WhatsApp at:
+91 8328053327
Mention the role you are applying for clearly (e.g., RA Associate EU OSD, FR&D Cost Projects, etc.).
💼 Perks of Working at Aurobindo Pharma
- 🌍 Opportunity to work in global regulatory environments
- 💸 Competitive salary with regular appraisals
- 🧑🔬 Work on challenging, innovative projects
- 🏥 Access to medical insurance and employee care
- 🔁 Exposure to international submissions and compliance workflows
🗃️ Additional Details
This is a verified hiring opportunity. Aurobindo Pharma is committed to being an equal opportunity employer, supporting diversity, inclusion, and a collaborative workspace.
📢 Whether you are a regulatory specialist, reviewer, or formulation development expert, this could be your chance to grow within one of the most respected pharma companies in India and abroad.
🖼️ Featured Blog Image
Image Description:
“Aurobindo Pharma is actively hiring professionals for Regulatory Affairs and FR&D roles – apply now and grow your pharmaceutical career with a global leader.”
📝 Summary Table
| Department | Role | Experience | Qualification | Key Focus |
|---|---|---|---|---|
| Regulatory Affairs | EU OSD Associate | 2–10 Years | M.Pharm | EU Regulatory Submissions |
| Regulatory Affairs | US & Canada Injectable | 2–10 Years | M.Pharm | FDA Submission & Compliance |
| Formulation R&D | Cost Improvement | 2–6 Years | M.Pharm | Cost-Effective Formulation |
| Regulatory Reviewer | CMC-SPD (US) | 2–6 Years | M.Pharm/B.Pharm | Document Review |
📢 Final Note
The pharmaceutical industry is evolving rapidly. Aurobindo Pharma offers a gateway to international experience, innovation, and impactful work in the healthcare domain. Don’t miss this chance to become a vital contributor to life-saving treatments around the world.
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