AUROBINDO PHARMA multiple positions open for Regulatory Affairs (US Market)
Embark on a career journey where your expertise in Regulatory Affairs isn’t just valued but celebrated.
With us, you’ll enjoy unparalleled opportunities for professional growth, a supportive work environment that fosters collective excellence, and the chance to make a real difference in patients’ lives.
We Are Hiring In Hyderabad!
POSITIONS OPEN FOR REGULATORY AFFAIRS EXPERT IN US MARKET:
• SPD – CMC
• OSD – CMC
• OSD – Post Approval
Position: SPD – CMC
Key Skills: Hands-on experience in handling the complete life cycle (from review, submission and queries to post approval) of Topical/Dermatological Formulations. Adherence to high quality, and regulatory standards in dossiers.
Experience: 3 – 6 years
Position: OSD – CMC
Key Skills: Preparation, review and compilation of assigned ANDA/NDA [505 b (2)] /projects for filing and knowledge of eCTD, Module 2 and 3. Hands-on experience in reviewing CMC documents of Solid and Liquid Oral Dosage forms.
Experience: 3 – 6 years
Position: OSD-Post Approval
Key Skills: This position is for the US regulatory team responsible for the Life Cycle Management of Approved and Tentative Approved ANDAS/NDAs [i.e., filing of supplements (CВЕ, СВЕ-30, PAS, Response to Queries, Controlled Correspondence, Annual Reports/ Updates etc.]
Experience: 3 – 6 years
Ready to be part of a team that’s committed to a healthier life? Apply now and unleash your potential with us. Share your applications at hrrc1@aurobindo.com.
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