Scientist II, Downstream Viral Vector Process Development

GeneFab

$130K — $150K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. or Master's in Chemical Engineering, Biochemical Engineering, Biotechnology, or related field (3 years with Ph.D., 5 with Master's).
  • Proven expertise in downstream process development for viral vectors, especially AAV and lentiviral vectors.
  • Hands-on experience with chromatography, filtration, TFF, and other processing techniques.
  • Strong analytical skills to interpret complex data sets effectively.
  • Excellent communication and teamwork skills.
  • Knowledge of regulatory requirements in biopharmaceutical manufacturing.
  • Preferred experience in formulation science.

Responsibilities

  • Design, optimize, and scale-up purification processes for viral vectors in gene therapy.
  • Execute experimental plans and analyze data for process efficiency and quality improvement.
  • Collaborate across teams for seamless integration of processes.
  • Troubleshoot and resolve technical challenges in downstream processing.
  • Present project status updates to internal teams and clients.
  • Stay updated on industry trends and regulatory guidelines to improve processes.
  • Provide leadership to development associates as the team grows.

Benefits

  • Opportunity to work in a cutting-edge field of gene therapy.
  • Hands-on role combining technical expertise with client interaction.
  • Collaborative environment within a project-based structure.
  • Leadership opportunities as the team expands.
  • Continuous learning with exposure to emerging technologies and industry trends.
Full Job Description
GeneFab is seeking an experienced Downstream Process Development Scientist/Lead focused on viral vector purification (AAV and Lentiviral) for in vivo gene therapy. It is a technical, project-based role within a CRDMO environment that balances hands-on process optimization with cross-functional leadership and client-facing responsibilities.

Responsibilities

  • Design, optimize, and scale-up downstream processes for the purification of viral
    vectors, with a focus on in vivo gene therapy products and lentiviral vectors.
  • Execute experimental plans, analyze data, and provide insightful
    recommendations to improve process efficiency, yield, and product quality.
  • Collaborate with cross-functional teams, including Upstream Process
    Development, Analytical Development, and Manufacturing, to ensure seamless
    integration of processes.
  • Troubleshoot and resolve technical challenges in downstream processes, ensuring
    robust and scalable solutions.
  • Present internally and to client with project status updates
  • Stay abreast of industry trends, emerging technologies, and regulatory guidelines
    to contribute to the continuous improvement of processes and compliance.
  • Provide direction and leadership to development associates as the team expands.


Qualifications

  • Ph.D. or Master's degree in Chemical Engineering, Biochemical Engineering,
    Biotechnology, or related field with a minimum of 3 years (Ph.D.) or 5 years
    (Master's) of relevant industry experience
  • Proven expertise in downstream process development for viral vectors, with a
    focus on AAV and lentiviral vectors.
  • Hands-on experience with chromatography, filtration, TFF and other downstream
    processing techniques.
  • Strong analytical and problem-solving skills, with the ability to interpret complex
    data sets.
  • Excellent communication skills and the ability to work collaboratively in a team
    environment.
  • Knowledge of regulatory requirements and quality standards related to
    biopharmaceutical manufacturing.
  • Experience with formulation science preferred


$130,000 - $150,000 a year

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