Gujarat

M.Sc / B.Pharm / M.Pharm; Finished, AMV and Stability Section, knowledge of Instrument - HPLC, GC. Preferably know-how of Chromeleon Software

A masters degree on a point scale wherever the grading system is followed with Ph.D. in a concerned, relevant, allied subject from an Indian University or an equivalent degree from an accredited Foreign University. 

Good exposure require in IPQA - OSD and Sterile, Qualification OSD and Sterile. Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.

B.Pharm, M.Sc, M. Pharm with 3-8 years of experience in IPQA and manufacturing, packing QMS related activities in oral solid dosage form tablets, capsules, soft gelatin capsules, pellet Dosage form manufacturing facilities.

Project entitled Exploring the potential of algal nutrients for cell growth and understanding its mechanism at a molecular level. M.Sc Biotechnology, Microbiology or relevant life sciences discipline with a minimum of 55% marks.

Preparation and review of test procedure, development reports, method validation protocol and LNBs. Perform calibration of the analytical instruments as per calibration schedule. Analytical method development, validation, and sample analysis for Extractables and Leachables using HPLC, LCMS, GCMS and ICPMS. Identification and characterization of unknown impurities by LCMS.

B.Sc. / B.Pharm/ M.Sc.; Hands-on experience in Analytical Method Validation, Method Transfer, Protocol Review, Analysis of CU, BU, Assay on HPLC & UV Spectrophotometer, BD, TD, PSD & Water Content, Tests are performed daily to daily on job.

Must know process validation cleaning validation verification and hold time studies. Candidate should also have exposure to EU, MHRA, and USFDA regulatory audits.

Pharmacist degree from a recognized institution, registration with Gujarat Pharmacist Council is required.