Posted:2 months ago| Platform:
Work from Office
Full Time
Role & responsibilities Responsible to receive, register and analyze batch samples and stability samples. Responsible to prepare reagents, buffers and test solutions as and when required. Responsible to operate, calibrate/ verify/ qualify HPLC, UPLC instruments. Responsible to execute the Analytical Method validations/verifications/Transfers Responsible to prepare SOPs, STPs, Protocols and other GMP documents Responsible to interpret and record the data / results accurately and contemporaneously. Responsible to report to superior any abnormalities found during routine activities Responsible to follow Hygiene, Safety, SOPs, GLP, GMP and GDP. Preferred candidate profile Adequate testing knowledge on Biologics/Monoclonal Antibodies Capillary Electrophoresis : CESDS-R, CESDS-NR HPLC : RP, SEC, Glycan, CEX, Ion exchange chromatography and Polysorbate 20 Maurice : charge variants by iCEF UPLC : Peptide mapping. Qualification and Experience : MSc Biotechnology/Biochemistry/Microbiology with 03-07 Years experience of Biosimilars/Biologics QC.
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5.0 - 12.0 Lacs P.A.