Location: Hyderabad, India (Multinational Operations)
Industry: Pharmaceutical Manufacturing
Job Type: Full-time
1. Job Description
Aurobindo Pharma Limited (APL), a global leader in generic pharmaceuticals, is seeking experienced Regulatory Affairs (RA) professionals for its EU/US/Canada markets. The roles involve ensuring compliance with international regulatory standards for Oral Solid Dosage (OSD) and Injectable products.
Key Responsibilities:
- Prepare and submit regulatory dossiers for EU, US, and Canada markets.
- Review drug formulations, labeling, and documentation for compliance.
- Coordinate with cross-functional teams for timely approvals.
- Stay updated with evolving FDA, EMA, and Health Canada guidelines.
Positions Available:
- RA – EU & US Regulatory Team (OSD)
- Experience: 3–10 years
- Qualification: M.Pharmacy
- RA – US & Canada Market Team (Injectable)
- Experience: 3–10 years
- Qualification: M.Pharmacy
2. About Aurobindo Pharma Ltd (APL)
- Ranking: 2nd largest generic company in the USA (by Rx volume).
- Global Presence: Operations in 34+ countries, exports to 155 nations.
- Revenue: USD 2.8 Billion (2018–19).
- Markets: Top 10 generic player in France, Germany, UK, Italy, and more.
APL is renowned for its high-quality, affordable medicines and robust R&D capabilities.
3. Eligibility Criteria
- Education: Master of Pharmacy (M.Pharm) mandatory.
- Experience: 3–10 years in Regulatory Affairs (OSD/Injectables).
- Skills: Proficiency in CTD/eCTD submissions, FDA/EMA guidelines, and teamwork.
4. How to Apply
Interested candidates can share their resume via WhatsApp:
- WhatsApp Number: +91 8328053327
- Format: Submit a PDF resume with subject “Application for RA Position – [EU/US/Canada] – [Your Name]”.
Note: Only shortlisted candidates will be contacted.
Why Join Aurobindo Pharma?
- Work with a globally recognized pharmaceutical leader.
- Career growth in regulatory compliance and drug approvals.
- Competitive salary and benefits.
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