Associate Scientist

July 16, 2025
$56 - $59 / hour
Apply Now

Apply for this job

Upload CV (doc, docx, pdf)

Job Description

Job Summary:

  • The primary focus of this Associate Scientist will be to support process development, production, and characterization of early and late-stage viral vectors (lentiviral vectors and/or adeno-associated viruses).
  • This position will be providing technical subject matter expertise with internal and/or external development and manufacturing collaborators for activities including tech transfer, process characterization, and pre-clinical or clinical process lifecycle management.

Duties and Responsibilities:

  • Design, execute, and troubleshoot upstream development experiments supporting next-generation LVV production.
  • Identify, onboard, and develop Client upstream technologies in collaboration with internal and external partners.
  • Provide experimental design and executional support to team members.
  • Support cross-functional development efforts e.g. downstream process development, high-throughput process development.
  • Generate representative crude harvest material to support downstream development activities.
  • Work independently and within teams to design, execute, and analyze experiments.
  • Maintain accurate and detailed laboratory notebook and documentation.
  • Summarize and present data in group meetings and contribute to group discussions and team strategy.
  • Author technical reports and study memos.

Education and Experience:

  • B.S. with 2+ years of experience or M.S. with 0-2 years of hands-on upstream experience.
  • Experience with suspension culture of mammalian cells in shake flasks and small stirred tank bioreactors.
  • Experience with transient transfection operations to produce viral vectors (e.g. adeno-, retro-, lenti).
  • Hands-on process development experience.
  • Degree in biological or chemical engineering, biochemistry, or bio-related field.
  • Experience in the development of viral vectors (e.g. adeno-, retro-, lenti-), including successful transfer for GMP manufacturing.
  • Experience with single-use technologies.
  • Independently motivated with ability to multitask, problem-solve, and coordinate activities within a team.
  • Ability to design experiments with design of experiment (DOE) approaches, perform experiments, and interpret the results using statistical software (ex. JMP).

Additional Job Requirements:

  • Lab w/o blood & animal.
  • Position Handles Hazardous Materials.