Are you passionate about making a difference in the pharmaceutical industry? Aurobindo Pharma Limited invites talented individuals to join our Regulatory Affairs department in various exciting roles. Take the opportunity to contribute to the advancement of healthcare by ensuring compliance and regulatory adherence in the US and EU markets.
Position 1: Research Associate/Scientist – Post Approval (US Market)
- Vacancies: 2
- Qualification: M Pharm – Any Specialization
- Experience: 3-6 Years
- Responsibilities: Handling post-approval activities, CB-0, CB-30, PASS, FDA Inspections.
Position 2: Regulatory Associate/Scientist – CMC (US Market)
- Vacancies: 3
- Qualification: M Pharm – Any Specialization
- Experience: 3-10 Years
- Responsibilities: Filing ANDAs, Annual Submissions, Dossier Preparations.
Position 3: Regulatory Associate/Scientist – Queries (US Market)
- Vacancy: 1
- Qualification: M Pharm – Any Specialization
- Experience: 8-10 Years
- Responsibilities: Handling queries for the US Market.
Position 4: Regulatory Associate/Scientist – Module 3 (EU Market)
- Vacancies: 5
- Qualification: M Pharm – Pharmaceutics / Regulatory Affairs
- Experience: 3-10 Years
- Responsibilities: CMC, Initial Submissions, Dossier Preparations, Pre/Post Submissions & Life Cycle Management.
Position 5: Regulatory Associate/Scientist – Module 1 (EU Market)
- Vacancy: 1
- Qualification: M Pharm – Any Specialization
- Experience: 3-10 Years
- Responsibilities: Administration, Preparation & Submission of renewals, Response to agency queries, RSI, RFI.
Contact Details: Interested candidates can send their profiles to SravanKumar.Bhimuni@aurobindo.com
Interview Details
- Date: Sunday, 02nd June 2024
- Time: 09:00 AM to 01:00 PM
- Venue: APL Research Center – 1 Bachupally, Coco Cola Road.
- Work Location: APL Research Center I Sy.No.313&314, Bachupalli, Hyderabad, Telangana-500090
