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Senior Research Associate, Analytical Development

United States - California - Santa MonicaProcess/Product Development & OperationsRegular

Descripción del trabajo


Responsibilities (include but not limited to):

  • Establish analytical methods to evaluate lentiviral and retroviral vector transduced samples for impurities, GC, IFU and VCN assays.
  • Perform qualification studies for Analytical methods per established guidance.
  • Author, review and approve technical documents including standard operating procedures, test methods, and technical reports.
  • Work with a cross-functional team to develop, adapt, execute, and document analytical methods to characterize the processes for manufacturing lots of drug substance and drug products.

Basic Qualifications:

  • Master’s Degree and 2+ years of industry experience OR
  • Bachelor’s Degree and 4+ years of industry experience OR
  • Associate Degree and 5+ years of industry experience OR
  • High School Degree and 6+ years of industry experience

Preferred Qualifications:

  • Experience with Mammalian cell culture
  • Experience with molecular biology techniques (transduction, titer, DNA/RNA extractions, cDNA synthesis, PCR, ELISA).
  • Analytical method development in one or more of the following:
    • Droplet digital PCR (ddPCR)
    • Realtime quantitative PCR (qPCR)
    • ELISA, MSD, Luminex
    • Viral titer, IFU assays
  • Experience with software including GraphPad, SoftMax, JMP, Geneious (or similar), MS Office suite
  • Proven ability to work in a fast-paced environment, meet deadlines, & prioritize work on multiple projects.
  • Strong attention to detail with the ability to handle multiple responsibilities simultaneously
  • Ability to work independently and as part of a team.
  • Strong interpersonal skills and communication skills including verbal and written communication are essential in this collaborative work environment
  • Occasional travel