Trailblazing Method Development: Lead the charge in developing and validating cutting-edge chromatography assays, harnessing your technical prowess to drive the success of preclinical and clinical studies.
Analytical Excellence: Execute study sample analysis with precision and accuracy, delving into toxicological and biological endpoints to uncover insights that shape the future of scientific research.
Meticulous Compliance: Navigate the intricacies of GLP regulations with finesse, ensuring all study work is conducted in strict accordance with regulatory standards while maintaining meticulous documentation at every step of the way.
Strategic Project Management: Take ownership of project timelines, orchestrating each phase with precision to ensure timely delivery and optimal outcomes.
Client Collaboration: Serve as a trusted scientific advisor to our clients, providing invaluable insights and assistance in study and assay design, and delivering exceptional service that exceeds expectations.
Innovative Methodologies: Stay ahead of the curve by participating in the validation and qualification of new and existing methods, pushing the boundaries of what's possible in preclinical research.
Leadership and Mentorship: Inspire and empower your colleagues as you provide supervision and guidance to laboratory staff, fostering a culture of excellence and collaboration.
MUST HAVE:
Masters or PhD in biological or pharmaceutical science,
Strong background in LC MS
Familiarity with LIMS and electronic notebooks
Experience in the biotech or pharma industry preferred