8 - 13 Years

Job Description

Experience in reputed Pharma company of independently handling ANDA/ EU/ AUS dossiers. Thorough knowledge of current regulatory requirement EU/US. Good communication skill written/oral.

Salary: Not Disclosed by Recruiter

Industry:Pharma / Biotech / Clinical Research

Functional Area:Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Role Category:Drug Regulatory Affairs/Documentation

Role:Regulatory Affairs Manager

Employment Type:Permanent Job, Full Time


Desired Candidate Profile

Please refer to the Job description above


UG:B.Pharma - Pharmacy, B.Sc - Any Specialization

PG:M.Pharma - Pharmacy, MS/M.Sc(Science) - Any Specialization

Company Profile

Centaur Pharmaceuticals Pvt. Ltd.

Centaur has a highly experienced Regulatory Affairs team for compilation of DMFs, CTD/eCTD Dossiers and ANDAs for submission to regulatory authorities globally including USA/ EU/AUS/JAPAN/CANADA/ SOUTH AFRICA/MEXICO/ NEW ZEALAND etc.

The regulatory team is continuously updated on the global regulatory framework for organizing data generation as per the required submission norms in the territory. Centaur Regulatory Team is working on submissions of DMFs and Dossiers globally which will pave business for Centaur in the coming years.

This will include domestic as well as emerging market opportunities and registration of Finished products and APIs in highly regulated and competitive markets globally.
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Recruiter Name:Neelam Bagwe

Contact Company:Centaur Pharmaceuticals Pvt. Ltd.