M.Pharm

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

BPharm or MPharm require; Review of Protocols and reports related to Analytical method validation, Verification of API and Finished product, Vendor qualification, cleaning validations. Hypothesis analysis, general validations, Stability, photo stability, thermal cycling, in use, split study and miscellaneous studies and approval in LIAAS where ever applicable.

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

A Post-graduate, Graduate degree in Chemistry, Pharmacy, Life Sciences. Candidate should have knowledge about Post-approval change submission requirement and compilation of variation packages for US, CAN, EU, AUS-NZ, ROW markets.

The candidate must have a postgraduate degree (M.S.,M.Pharm.,M.Sc.) in Pharmacology from a PCI, AICTE, UGC, NAAC recognized, accredited University, Institute with a minimum of 60% marks. The candidate must have cleared GPAT, GATE, CSIR-NET or any National entrance test exam conducted by any Central Govt. agency at the time of the interview, selection process. 

Experience in Documentation, Issuance, CCF, Trackwise, SOP preparation, well versed with GMP and Regulatory requirements of USFDA, EU, ANVISA, AQA.