4-5

Sun Pharma is the fourth largest specialty generic pharmaceutical company in the world. We provide high-quality, affordable medicines trusted by healthcare professionals and patients in over 150 countries.

Dossier submission and review of Module 1, 2 and 3. ANDA submission. DCP, MRP, National Filing for various EU countries. 

MSc, M.Tech, M.Pharm. in relevant stream of Biological Sciences with 3-5 years of relevant experience in Analytical R&D, QC department of Biopharmaceutical industry.

Bachelors or Masters degree in Pharmacy, Pharmaceutical Sciences. Lead and manage the technology transfer of pharmaceutical formulations from R&D to manufacturing Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs

Bachelors or Masters in Pharmacy. Must have exposure in handling of Process Area maintenance like Manufacturing Vassals, Filling machine, Autoclave, Isolators and Lyophilization.

M. Pharm / M. Sc / B. Pharm / B. Sc; Experience in Method Validations and Verifications, Analytical Method Transfers with Brazil Regulatory exposure. Experience in Finished Product, In-Process, Stability and GLP activities

M.Pharm; Analytical Method Validation. Development, Transfer activities. Calibration of the Analytical instruments like HPLC, GCHS, IR, UV & Disso as per the master calibration schedule

M.Pharmacy/M.Sc Chemistry B.Pharmacy; Having injectable experience of Shop floor Supervising Activities like Component Preparation, Aseptic Filling, Compounding Operations, BMR Review and QMS Exposure.

M.Pharm, B.Pharm, M.Sc, B.Sc; Chemist and Analysts, Microbiologists, Validation; GLP Section -SPEC/STP Preparation, LIMS Documentation