Aurobindo Pharma Careers 2025 – Regulatory Affairs & FR&D Jobs | Apply Now

Explore career opportunities at Aurobindo Pharma Limited for Regulatory Affairs and Formulation R&D roles in 2025. Openings for M.Pharm professionals in RA (EU/US/Canada) & FR&D teams.

Aurobindo Pharma Recruitment 2025: Openings in Regulatory Affairs & FR&D – Apply Now!

Aurobindo Pharma Limited, a global leader in generic pharmaceutical manufacturing, is actively hiring for critical positions in Regulatory Affairs (RA) and Formulation Research & Development (FR&D) departments. If you’re an experienced pharmaceutical professional looking to grow your career with one of India’s most reputable pharma companies, this is a golden opportunity.

🌍 About Aurobindo Pharma Ltd

Aurobindo Pharma Ltd (APL) is an Indian multinational pharmaceutical manufacturing company, with an impressive global footprint and a strong portfolio of high-quality generic products. With over US$2.8 billion in revenue for FY 2018-19, APL has established a robust presence in more than 34 countries and exports to over 155 nations worldwide.

Key Highlights:

• 2nd Largest Generic Company in the USA (as per Rx dispensed)

• Ranked among the Top 10 Generic Players in Europe: France, Germany, UK, Portugal, Italy, Czech Republic, Netherlands & Belgium

• Renowned for compliance, innovation, and cost-effective medicines

🎯 Current Job Openings at Aurobindo Pharma

1. Position: Regulatory Affairs – EU Regulatory Team (OSD)

• Experience Required: 2 to 10 years

• Qualification: M.Pharmacy

• Location: Hyderabad

• Key Responsibilities:

  • Handle regulatory submissions and lifecycle management for oral solid dosage forms in EU markets

  • Expertise in CTD Module preparation, review, and submission

  • Interface with cross-functional teams to ensure regulatory compliance

2. Position: Regulatory Affairs – US & Canada Team (Injectables)

• Experience Required: 2 to 10 years

• Qualification: M.Pharmacy

• Location: Hyderabad

• Key Responsibilities:

  • Lead regulatory filings and submission strategies for injectable formulations targeting US & Canadian markets

  • Deep knowledge of ANDA/NDA pathways, eCTD submissions, and FDA regulatory guidelines

  • Review change controls, support queries, and manage post-approval changes

3. Position: FR&D – Cost Improvement Projects (OSD)

• Experience Required: 2 to 6 years

• Qualification: M.Pharmacy

• Location: Hyderabad

• Key Responsibilities:

  • Formulation development and optimization of oral solid dosage (tablets/capsules)

  • Execute cost-improvement strategies through innovative formulation techniques

  • Collaborate with AR&D, QA, RA, and production for smooth tech transfer

4. Position: Regulatory Affairs Department – CMC-SPD Reviewer (US)

• Experience Required: 2 to 6 years

• Qualification: M.Pharm / B.Pharm

• Location: Hyderabad

• Key Responsibilities:

  • Review of CMC sections of regulatory submissions for the US

  • Analyze data from formulation development, stability, and validation studies

  • Ensure data integrity, compliance with FDA standards, and completeness before submission

✅ Who Should Apply?

If you have:

• A master’s degree in pharmacy (mandatory for most roles)

• Experience ranging from 2 to 10 years in relevant pharmaceutical functions

• A passion for regulatory compliance, drug development, and formulation optimization

…then Aurobindo Pharma’s latest hiring drive is ideal for you.

📌 How to Apply?

Interested candidates can send their latest updated resume directly via WhatsApp to the below contact:

📱 WhatsApp Number: 8328053327

Ensure your resume includes:

• Your updated contact information

• Detailed employment history

• Educational qualifications

• Any relevant certifications or publications

📝 Why Choose Aurobindo Pharma?

Working at Aurobindo offers more than just a job—it’s a platform for long-term career growth, global exposure, and the opportunity to contribute to affordable healthcare.

Perks of Joining Aurobindo:

• Be a part of a fast-growing global organization

• Opportunities to work with world-class manufacturing and R&D facilities

• Exposure to USFDA, MHRA, WHO-GMP, and EU GMP-compliant plants

• Strong support for learning, innovation, and continuous improvement

💡 Tips for Applicants

• Customize your resume to highlight experience in RA, FR&D, or injectable/OSD domains

• Emphasize knowledge of CTD/eCTD, ANDA, QbD, and ICH guidelines

• Be prepared to discuss your past regulatory submissions or formulation work during interviews

• Showcase cross-functional collaboration in previous roles

📍 About Aurobindo’s Global Impact

• Operates 6 R&D centers and 25+ manufacturing facilities

• Filed over 400+ ANDAs, with a robust pipeline of niche and complex products

• Committed to corporate social responsibility and sustainable manufacturing

Aurobindo is more than just a company—it’s a mission-driven organization focused on making healthcare accessible worldwide.

Aurobindo Pharma’s 2025 recruitment drive is an exceptional opportunity for professionals in the Regulatory Affairs and Formulation R&D space to elevate their careers in a high-impact, innovation-led environment.

📢 Don’t miss your chance! Send your CV to WhatsApp number 8328053327 today and take the next big step in your pharma journey with Aurobindo.