Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India. The company manufactures generic pharmaceuticals and active pharmaceutical ingredients.
Post : Research Associate / Scientist
Department : Regulatory Affairs
Division : APL RC I
Location : Bachupally
Post Approval Module (US Market)
No of post : 2
Qualification : M.Pharm - Any Specialization
Experience : 3-6 years, Handling postapproval activities,CB-0,CB-30, PASS, FDA Inspections.
CMC Module (US Market)
No of post : 3
Qualification : M.Pharm - Any Specialization
Experience : 3-10 Years, Handson experience in filing ANDAs,Annual Submissions,Dossier Preparations.
Queries Module (US Market)
No of post : 01
Qualification : M.Pharm - Any Specialization
Experience : 8-10 Years, Hands on experience in handling queries for US Market.
Module 3 (EU Market)
No of post : 5
Qualification : M.Pharm** - Pharmaceutics /Regulatory Affairs
Experience : 3-10 Years, Hands on experience in CMC, Initial Submissions, Dossier Preparations, Pre / Post Submissions & Life Cycle Management.
Module 1 (EU Market)
No of post : 1
Qualification : M.Pharm - Any Specialization
Experience : 3-10 Years, Hands on experience in Adminstration, Preparation & Submission of renewals, Response to agency queries, RSI,RFI.
Walk in Interview
Date : 02nd June 2024
Time : 09.00 am to 01.00 pm
Venue : APL Research Center - I Bachupally, Coco Cola Road. Sy.No.313&314, Bachupalli, Hyderabad, Telangana-500090
Interested candidates can send their profiles to SravanKumar.Bhimuni@aurobindo.com
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