Job Description
Walk-In Drive (50 Openings) for Regulatory Affairs Dept.-R&D Center On 21st Nov’ 2020
Collecting and reviewing the documents received from various departments R&D, AR&D,QA,QC and Production etc at each and every stage of manufacturing of drug substances to minimize the errors at the time of submission to regulatory agencies. Hands on experience on the preparation of DMFs and their registration processes in the major regulatory regions [US, Canada, Europe etc].. Hands on experience on preparation of drug master files, Applicants Parts, Tech Pack, life cycle management [updates and amendments] and drafting of response to deficiencies and customer DMF review comments for all global regions. Should have hands on experience on eCTD regulatory submission tools. Should have Knowledge on the requirements to respond to the deficiencies. Participation in the cross functional team meeting and providing regulatory input to the Product Development Teams.
Job Title: Executive Trainee / Executive
Department : Regulatory Affairs-API
Qualification: B.Pharma/ M.Pharma/ M.Sc
Experience: Should have minimum of 2 to 8 years of experience in API Regulatory Affairs
Openings : 50
Time & Venue Details: Walk-Ins On 21st November 2020 from 9.00 AM to 1.00 PM , Venue Details: MSN Laboratories Pvt. Ltd., R&D Center, Plot No 12, Phase-IV, Sy.no.119, IDA Pashamylaram, ptancherru Mandal, sangareddy Dist Hyderabad, Ph No : +91-8452304702/4789 (view on Map).
Work Location: MSN LS II (Chegunta , Chandampet).
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MSN Laboratories Pvt. Ltd-Walk-In Drive (50 Openings) for Regulatory Affairs Dept.-R&D Center On 21st Nov’ 2020