Senior Scientist - Downstream Process Development

NovartisDurham, CA
$119,700 - $222,300Hybrid

About The Position

Join the team shaping the future of Cell and Gene Therapy and help bring transformational medicines to patients worldwide. As a Senior Scientist – Downstream Process Development, you will play a critical role in advancing viral vector technologies across adeno-associated virus (AAV) and lentiviral vector (LVV) platforms. Combining scientific expertise, innovation, and hands-on laboratory leadership, you will drive process development strategies that support breakthrough therapies from pre-clinical development through clinical manufacturing. This is a unique opportunity to influence cutting-edge science, collaborate with world-class experts, and accelerate the delivery of life-changing treatments to patients with urgent unmet needs.

Requirements

  • Bachelor’s degree in biological sciences, pharmaceutical sciences, chemical engineering, or a related technical field with 8+ years of relevant experience; Master’s degree with 6+ years of relevant experience; or PhD with 4+ years of relevant experience.
  • Strong technical background in downstream process development for biologics and/or viral vector-based therapies, with hands-on experience designing, executing, and interpreting process development studies.
  • In-depth expertise across multiple downstream unit operations such as chromatography, depth filtration, precipitation or flocculation, tangential flow filtration, ultracentrifugation, impurity clearance, and adventitious virus clearance.
  • Proficiency in statistical analysis principles, Design of Experiments (DoE), and data-driven decision-making.
  • Proven ability to define technical plans, solve complex process development challenges, and deliver scientific objectives within program timelines.
  • Demonstrated ability to influence cross-functional stakeholders, communicate technical recommendations clearly, and contribute to program strategy in a matrixed environment.
  • Innovative mindset with experience advancing continuous improvement, technical standards, best practices, or platform approaches across programs.

Nice To Haves

  • Data Science
  • Materials Science
  • Process Simulation
  • Technical Writing
  • Waterfall Model

Responsibilities

  • Serve as the downstream technical lead for one or more gene therapy programs.
  • Define the overall downstream development plan for assigned gene therapy programs.
  • Design, execute, and interpret downstream process development studies.
  • Perform hands-on process operations at both small scale and large scale.
  • Collaborate with cross-functional teams to advance AAV and LVV programs from pre-clinical development through clinical manufacturing.
  • Deliver high-quality experimental outputs within program timelines.
  • Apply a strong statistical and data-driven mindset to analyze process study results, draw scientifically sound conclusions, and inform development strategy.
  • Drive downstream innovation by evaluating emerging technologies, current scientific advances, and state-of-the-field approaches relevant to viral vector process development.
  • Promote adoption of technical standards, platform approaches, and best practices across multiple programs and modalities.
  • Author technical reports, summarize process development outcomes, and contribute downstream content to regulatory filings, including IND submissions.
  • Present study results, technical recommendations, and development strategies to internal and external stakeholders in cross-functional forums.
  • Be a technical coach and mentor, fostering an innovative, collaborative, and scientifically rigorous culture.
  • Present technical recommendations and mentor colleagues to foster scientific excellence and collaboration.

Benefits

  • Relocation Support
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