GENPHARMA
WORK AS MANAGER - REGULATORY AFFAIRS
About Company,
GenPharma is a GMP approved pharmaceutical company having its state of art manufacturing Units in Pune and have global presense in Pharmaceutical Formulations.
Job Description:
1.all Regulatory Documentation.
2.Preparing Dossiers, Review and Filling of Dossiers.
3.Registration in Semi regulated and Regulated Markets.
4. Dossiers preparation for non regulated markets.
Candidate Profile:
Candidate must be B.Pharma/M.Pharma with 7-8 yrs of relevant experience in handling international regulatory affair for Formulation.
Exposure to Compilation and submission to FDA eCTD/CTD compilation.
Additional Information:
Experience: 7-8 years
Location: Pune
Education: B.Pharma, M.Pharm
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Healthcare, Medical, R&D
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