2-3

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

The CRA is as such responsible for recruitment at site level. The CRA thereby delivers results that have a direct impact on the successful completion of the clinical programme.

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.

Candidate should have Exposure of Fette, Sejong, Legacy, Korsch, Cadmach or any other machine having Automatic Weight Control , Compaction Force Control etc.

M.Pharm, B.Pharm, MSc Chemistry, Biotechnology, Life science, Microbiology, BSc, B.Tech Electrical, Mechanical, Instrumentation, Biotechnology, Diploma.

Executing chemical reactions in mg to gm scale and to synthesize required quantities of molecules/ compounds as per client specifications using efficient route and techniques

M.Pharm, B.Pharm, M.Sc. LLS has following openings for its EU-GMP Approved Global Standard OSD & Semi-solids Formulation manufacturing facility at Akola.