Aurobindo Pharma
At Aurobindo Pharma, we believe that innovation and compliance go hand in hand. As a leading global pharmaceutical company, we are committed to delivering high-quality, affordable medicines to millions across the world. To strengthen our regulatory team, we are inviting experienced professionals to be a part of our growth journey.
We are currently hiring for Regulatory Affairs (RA) professionals specialized in the Canada Market at our APLRC1 facility in Bachupally, Hyderabad.
Why Aurobindo?
Aurobindo Pharma is recognized for its strong pipeline of products, robust R&D capabilities, and commitment to global regulatory standards. Our team is driven by a shared mission: to improve access to healthcare through scientific excellence and operational integrity.
This role offers a unique opportunity to work on complex regulatory submissions, interact with cross-functional teams, and contribute to the successful commercialization of pharmaceutical products in a regulated market like Canada.
Position Overview
🔹 Role: Regulatory Affairs – Formulations (Canada Market)
🔹 Location: APLRC1, Bachupally, Hyderabad
🔹 Experience Required: 3 – 5 Years
🔹 Qualification: M.Pharmacy in Pharmaceutics, Pharmaceutical Technology, or Quality Assurance
What We’re Looking For
We’re seeking individuals who not only have hands-on experience in regulatory submissions but also possess the ability to interpret regulatory expectations and collaborate effectively with R&D and QA teams.
Desired Skills & Expertise:
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Proven experience in Regulatory Affairs – Canada Market, particularly Quality Modules
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Strong command of Regulatory Guidelines, Health Canada expectations, and submission strategies
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Sound understanding of pharmaceutical development processes for effective document review
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Familiarity with post-approval variation requirements
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Basic knowledge of Quality Assurance (QA) practices to ensure compliance in manufacturing documentation
Key Responsibilities
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Prepare and Review Submissions
Independently manage Module 2 and 3 regulatory submissions, ensuring technical accuracy and regulatory compliance. -
Regulatory Interpretation
Stay updated with Health Canada’s evolving guidelines and apply them effectively during the review cycle. -
Cross-Functional Collaboration
Work closely with R&D to evaluate formulation development documents, and coordinate with QA teams for accurate plant documentation. -
Post-Approval Activities
Handle regulatory changes and variations post-approval, ensuring timely updates and minimal market disruption.
Ready to Make an Impact?
If you’re passionate about regulatory affairs and looking to grow with a company that values expertise and innovation, we want to hear from you!
Send your resume to:
📧 sreeja.yangam@aurobindo.pharma.com
Be a part of something meaningful. Help us ensure that life-saving medicines reach patients safely, efficiently, and globally.
To apply for this job email your details to sreeja.yangam@aurobindo.pharma.com.
