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VDC Engineer - Milford

NGM Biopharmaceuticals

VDC Engineer - Milford

South San Francisco, CA
Paid
  • Responsibilities

    NGM Biopharmaceuticals, Inc. is a clinical stage biotech company dedicated to discovering and developing the next generation of medicines for the treatment of serious diseases.  Our experienced scientific team has joined forces with an impressive group of industry professionals, Nobel Laureates and other distinguished researchers to form a company where innovation and cutting-edge science has provided the foundation for a robust drug discovery engine.  To date, NGM Bio has generated a pipeline of seven drug candidates in various stages of development targeting liver, metabolic and ophthalmic diseases and cancer. The most advanced drug candidate, NGM282, is entering Phase 2b clinical studies in non-alcoholic steatohepatitis (NASH).  NGM’s strategic collaboration with Merck, which was extended to March 2022, will continue to provide us with the resources and flexibility to pursue our ambitious R&D goals and further extend our pipeline of novel drug candidates.  

    NGM Biopharmaceuticals, Inc. is seeking a highly motivated Research Associate to join our Nonclinical Safety development group. This will be a temp to full time position.

    Required Skills

    • Ability to perform techniques for in vivo mouse and/or rat studies, including animal handling, dosing, evaluation of clinical signs, necropsy and tissue collection
    • Ability to accurately record data in study files
    • Detail oriented with strong documentation and organizational skills
    • Excellent interpersonal skills, ability to work collaboratively and develop relationships with key stakeholders
    • Excellent communication skills

    Required Experience

    • BS degree in life science
    • 1+ years of relevant experience performing in vivo studies in an academic, contract research organization or pharmaceutical industry setting
    • Proven competency performing in vivo techniques in rodents, including animal handling, dosing, clinical observations and necropsy
    • Experience using software such as Excel, Prism and JMP
    • Proven ability to work independently and be self-motivated
  • Qualifications
    • Ability to perform techniques for in vivo mouse and/or rat studies, including animal handling, dosing, evaluation of clinical signs, necropsy and tissue collection
    • Ability to accurately record data in study files
    • Detail oriented with strong documentation and organizational skills
    • Excellent interpersonal skills, ability to work collaboratively and develop relationships with key stakeholders
    • Excellent communication skills