Walk-In Drive for Regulatory Affairs Dept. in
API Division- R&D Center
Job Title: Executive / Senior Executive Experience:
2 to 8 years in API RA field
Education: B.Pharma / M.Pharma
/ M.Sc
Department: Regulatory Affairs
Job Title: Executive / Senior Executive Experience: 1 to 6 years in API RA field Education: M.Sc
Department: Regulatory Affairs
Job Profile:
1. 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.
2. Hands on experience on the preparation of DMFs and their registration processes in the major regulatory regions [US, Canada, Europe etc]..
3. 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.
4. Should have hands on experience on eCTD regulatory submission tools.
5. Should have knowledge on the requirements to respond to the deficiencies.
6. Participation in the cross functional team meetings and providing regulatory inputs to the Product Development Teams.
Department: Regulatory Affairs
Job Title: Executive / Senior Executive Experience: 1 to 6 years in API RA field Education: M.Sc
Department: Regulatory Affairs
Job Profile:
1. 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.
2. Hands on experience on the preparation of DMFs and their registration processes in the major regulatory regions [US, Canada, Europe etc]..
3. 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.
4. Should have hands on experience on eCTD regulatory submission tools.
5. Should have knowledge on the requirements to respond to the deficiencies.
6. Participation in the cross functional team meetings and providing regulatory inputs to the Product Development Teams.
Position: Executive /Senior Executive / Junior
Manager
Date of Interview : 19.10.2019 (Saturday )
Interview Time : 9.00 AM to 1.00 PM
Venue Details :
MSN Laboratories Pvt.Ltd.,
R&D Center, Pashamylaram
Ph No : +91-8452304799/4899
040-30438786
Work Location : R&D Center & LS -II
Interview Time : 9.00 AM to 1.00 PM
Venue Details :
MSN Laboratories Pvt.Ltd.,
R&D Center, Pashamylaram
Ph No : +91-8452304799/4899
040-30438786
Work Location : R&D Center & LS -II
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