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AGC Biologics

End-to-end biopharma CDMO for gene therapies

Senior Scientist - Upstream, Late-Stage Process Development

Bioprocess & BiomanufacturingPosted on Nov 10
Full-timeCopenhagen, DenmarkNo salary listedIn-person

About the Job

Requirements

  • Hold a Bachelor's, Master's, or PhD degree in biotechnology, biochemical engineering, or another relevant scientific discipline.
  • Have at least five years of relevant industry experience with a Master's degree or two years with a PhD, or an equivalent combination of education and experience.
  • Have solid experience with mammalian cell culture processes, including bioreactor operations and scale-up.
  • Have experience with late-stage process development, such as process characterization, scale-down models, or technology transfer.
  • Be able to design studies, apply statistical methods, interpret complex data, and communicate scientifically sound conclusions.
  • Have experience with process risk assessments and preparing clear scientific reports and technical documentation.
  • Be fluent in written and spoken English.
  • Work independently, take responsibility for commitments, maintain scientific quality, structure work, and prioritize competing tasks when requirements change.
  • Discuss scientific findings with clients, explain recommendations, and work with others to resolve challenges.

Responsibilities

  • Plan and lead process characterization studies, including experimental design, data evaluation, and preparation of process characterization work reports.
  • Design and evaluate down-scale model qualification studies to demonstrate representativeness of manufacturing-scale processes.
  • Apply statistical methods, including Design of Experiments, and tools such as JMP to support data-driven scientific conclusions.
  • Contribute to FMECA and other process risk assessments to identify critical process parameters and support control strategy development.
  • Support late-stage development activities, including Limit of In Vitro Cell Age studies, Working Cell Bank activities, scale-up, and technology transfer.
  • Provide scientific guidance to laboratory technicians, collaborate across functions, and communicate technical findings, project status, and recommendations to clients.
  • Contribute to technical documentation, including development reports, technology transfer documentation, and relevant regulatory submissions.

Desired Qualifications

  • Experience with JMP, Design of Experiments, AMBR250, down-scale model qualification, FMECA, statistical equivalence testing, process modelling, or regulatory submissions.

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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