Ankleshwar

B.Sc. / M.Sc. (Life Sciences, Biotechnology, Microbiology, Biochemistry) B.Pharm / M.Pharm B.E. / B.Tech (Biotechnology, Chemical) 

To Check Qualities & Raw material lots before charging. Comply with all cGMP or any other regulatory requirements, including EHS requirements.

Experience in analysis of RM/Finish/ln Process/Stability samples by using instruments like HPLC, UV, Dissolution apparatus, GC, IR and AAS and Documentation related to QMS.

Review of the Equipment Verification qualification documents, Periodic review report, Performance requalification and Annual utility review reports. Documentation , compliance. Zydus

Dissolution apparatus, GC, IR and AAS and Documentation related to QMS. To review respective GMP Documents of QC department such as analytical / worksheet of In Process and Finished Product.

Compounding, Blending, Batch Manufacturing, ESP, Filling, Sea ling, Vial Washing.

Cadila Pharmaceuticals is an Indian multinational pharmaceutical company based in Ahmedabad. The company's operations focus on manufacturing products ranging from active pharmaceutical intermediates.

Trigger out of specification investigations upon detection of test results outside predefined specifications. Design and execute tests to confirm or rule out suspected root causes.

Rusan is a research driven pharmaceutical company having its Manufacturing Units in India and Worldwide Marketing of Pharmaceutical Formulation, Active Pharmaceutical Ingredients and Intermediates.