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AGC Biologics

End-to-end biopharma CDMO for gene therapies

Process Development Associate 3

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeBothell, WA, USAIn-person

About the Job

Requirements

  • A bachelor's degree with 5 or more years of relevant experience is required; equivalent education and experience may be considered.
  • Experience with mammalian or microbial cell culture and associated laboratory techniques is required.
  • A strong understanding of mammalian cell culture and/or microbial fermentation processes is required.
  • Ability to analyze data and apply scientific principles to process development challenges is required.
  • Strong written and verbal communication skills are required.
  • Ability to communicate complex technical information and recommendations effectively is required.
  • Strong collaboration and relationship-building skills across functions and with clients are required.
  • Ability to support and mentor less-experienced team members is required.

Responsibilities

  • Execute bench-scale bioreactor, fermenter, and shake-flask studies to develop and optimize upstream processes.
  • Support experimental design, including Design of Experiments, and analyze and interpret study results.
  • Lead or support the transfer and implementation of new technologies and systems into GMP operations.
  • Support equipment acquisition, installation, and implementation activities.
  • Provide technical problem-solving support and collaborate with cross-functional teams.
  • Represent Upstream Process Development on client project teams and support project planning and execution.
  • Present technical data and recommendations to clients and internal stakeholders.
  • Author protocols, technical reports, and supporting documentation.
  • Lead or support multiple projects, initiatives, and workstreams with varying levels of complexity.
  • Support technical decision-making in accordance with established processes and procedures.

Desired Qualifications

  • Experience with aseptic cell culture techniques or microbial fermentation.
  • Knowledge of large-scale manufacturing operations and technology transfer activities.
  • Client-facing experience.

About the Company

AGC Biologics

End-to-end biopharma CDMO for gene therapies

AGC Biologics is a global contract development and manufacturing organization (CDMO) that develops and manufactures biopharmaceuticals, including therapeutic proteins, plasmid DNA, viral vectors, and cell therapies. It offers end-to-end services from early development through commercial-scale manufacturing, with fast-track options for orphan drugs and rare diseases. The company runs cGMP-compliant facilities across the US, Europe, and Asia, recently expanding with a Longmont, Colorado site focused on cell and gene therapies. Its goal is to help biopharma partners bring new treatments to market efficiently and safely by providing integrated development and manufacturing, supported by its international footprint and project acceleration capabilities.

Company size
1,001-5,000
Company stage
Acquired
Total funding
$557.7M
Headquarters
Bothell, WA
Founded
2001

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