WORK AS MANAGER - REGULATORY AFFAIRS
GenPharma is a GMP approved pharmaceutical company having its state of art manufacturing Units in Pune and have global presense in Pharmaceutical Formulations.
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 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.
Experience: 7-8 years
Education: B.Pharma, M.Pharm
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Healthcare, Medical, R&D