3-4

B. Pharm , M.Sc. , M. Pharm with 2-8 years of relevant experience in IPQA , validation , Documentation related activities in Oral Solid,Oral Liquid,Semi Solid dosages manufacturing facilities.

M.Pharm, B.Pharm, M.Sc, B.Sc, QMS, Investigation, OS, OT, GLP, stability, finished product, analytical validation and transfer, IPQA in quality.

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