Job responsibilities: Develop, validate and perform Pharmacokinetics and Anti-drug Antibody assays in compliance with GLP guidelines and ISO17025 requirements Design new method validation or refine current method in response to changing requirements of drug development. Gather data and perform statistical analysis, interpret and communicate findings in reports or formal presentations Provide technical and scientific expertise to enable proper operation and maintenance of equipment as required Assist project management team in dossier writing and provide technical advice to project team Perform review of reports and SOPs Perform other tasks as assigned by the Divisional HeadJob requirements BSc or MSc in biomedical science, life science or equivalent Prior research and development experience are required. Knowledge in method validation, GLP and ISO17025 is a plus. Proficient with office management software (MS office, Teams), and statistical tools (Prism, SPSS, or PLA) Proficient in ligand binding assay platforms, including ELISA, cell-based bioassays Good understanding of method development and validation parameters Good interpersonal skills Good written and verbal communication skills Superior problem solving and troubleshooting skills, attention to details
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