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Overview:
Support in vitro ADME bioanalytical activities to generate high-quality DMPK data for drug discovery projects. Work under senior guidance to execute assays, operate LC-MS/MS systems, and develop technical expertise.
Key Responsibilities:
Operate and maintain LC-MS/MS instruments; assist with troubleshooting and data analysis.
Execute in vitro ADME assays: permeability (Caco-2/MDCK/PAMPA), metabolic stability (hepatocytes/microsomes/CYP inhibition), and physicochemical studies (solubility, Log D, stability in plasma/buffer/SGF/SIF).
Support metabolite identification (MET-ID) sample analysis and reporting.
Maintain accurate documentation, sample tracking, and project timelines.
Participate in training and mentorship to build technical proficiency.
Qualifications:
Education: M. Pharm in Pharmaceutical Analysis, Pharmaceutics, or related life science field.
Experience: 35 years in bioanalysis or DMPK/ADME, preferably in pharma/CRO.
Skills: Hands-on LC-MS/MS experience; familiarity with ADME assays, data software (e.g., Analyst, MassLynx), and GLP practices.
Attributes: Detail-oriented, strong learner, collaborative team player.
Job ID: 145102973