M.Pharm

Having Experience in Environmental Monitoring, Water Testing, In process Sampling, Analysis of Bulk Water, Finished and API by MLT, Bioburden, BET, Sterility, PET and Antibiotic Assay.

To handle all kind of lab instruments and experience to perform AMV and Documentation EM Monitoring, Water testing. Trend preparation, Microbial Testing, SOP and Protocol and other micro related activity

M.Sc. in Organic Chemistry, Analytical Chemistry Or M.Pharmacy in Pharmaceutical Analysis. Experience on the analysis of small organic molecular using various analytical techniques such as HPLC, MS, etc.

Masters in Pharmaceutical Science, Pharmaceutics, Pharmaceutical Technology, Industrial Pharmacy, Analytical Chemistry, with First class or equivalent grade at the preceding degree B. Pharm, B.Sc with a good academic record throughout. The CoE will primarily focus on the development and research of Novel Drug Delivery Systems (NDDS), creating a collaborative platform where academic expertise and cutting-edge research converge to drive innovation in this critical area of pharmaceutical science.

B.Pharm / M.Pharm; To perform equipment qualification, utility qualification activity with proper documentations. To perform Computer system validation. To investigate deviation, change request, OOS, market complaint etc.

Create and review regulatory documentation for Drug, Device and Combination product renewals and other life cycle maintenance-related submissions. Track status and progress of regulatory documentation.

M.Sc. Degree in Clinical Trial abd Research, Pharmacology, Biostatistics, Biochemistry, Pharmaceutical Sciences or or equivalent qualification from a recognized University, Institution OR M.Sc. Clinical Research with experience in teaching, research in niversity, college and or research experience at equivalent level with at least 3 publications in National, International Journals 

Lab Exposure, Analytical Method Validation. Review of Specification. Method of Analysis Protocol Handing of 00S and 00T. Investigation and Lab event. Review & Approval of QC Documents. Knowledge of Qualification and Validation related Activities. Audit Trail Review etc 

Execute the Formulation Technology Transfer activities across all Cipla sites and CMO to standardize, strengthen and improve the technology transfer processes and systems in line with regulations