Proven track record of documentation review for accuracy and compliance to procedures essentially in analytical methods development, validation, transfer, stability studies, Design & Development.
Syngene is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit.
M.Sc. Biotechnology, M.Pharm, Biotechnology with first class and preferably GPAT qualified. Experience in cell culture, basic molecular biology techniques
Good knowledge in monitoring compliance by GSK and Third Parties with PVASC by carrying out routine reconciliations and compliance checks and communicating standard information to Third Parties as required with appropriate guidance.
M.Sc. / M Pharm / PhD. Syngene is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
etermine biocompatibility testing required to demonstrate product safety. Document risk assessments in Baxter qualified systems such as Team Center Unified, Trackwise 8, Electronic Laboratory Notebook. Generate protocols and reports for biocompatibility testing.
Master of Science in Chemistry, Analytical Chemistry or Master of Pharmaceutical Sciences in Chemistry, Analytical Chemistry, from a recogniozed University, Institution.