4-5

Bachelor or Master degree Biotechnology, Pharmacy, Science or Ph. D Biotechnology, Biological Sciences or equivalent. Minimum 3-5 Years of experience in Pharmaceutical Industry with major experience in Regulatory Sciences group handling new submissions and, or LCM submission to global health authorities especially USFDA, EMA and other EU authorities.

Gl QC documents review, QMS and trainings, GLP and Standards Management Packing materials sampling and testing, LIMS masters preparations & Review.

Great opportunity for Diploma Pharmacy, Diploma fresher candidate to make their career in Pharmaceutical Industry and to work with Production Department as a Trainee Technical Assistant.

Competent in Analytical methods validations and transfers of Drug substances and Drug Products. Experience in drafting investigation reports and protocols

Review of specification, Method of analysis Protocol, heanding of OOS and OOT, Investigation and lab event, review and approval of QC documents.

Candidate should have exposure in analysis of Content Uniformity, Blend Uniformity, Hold Time Study, Cleaning Validation Test and Finish Product Analysis.

Exposure of analysis for Finished Products, Stability Samples & Raw Materials. Having Knowledge of Analytical Method Validation, Verification & Method Transfer. Having skill for data interpretation, troubleshooting. Pharma knowledge of Solid orals & Quality process.

Cliantha Research, a full-service Clinical Research Organization, is a leading provider of Clinical research services, based in Ahmedabad, India.

To perform all associate activities like reagent preparation, volumetric solution preparation, test solution preparation, factor determination, working standard preparation required for analysis as per approved procedure.