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AGC Biologics

End-to-end biopharma CDMO for gene therapies

Principal Technician

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

About the Job

Requirements

  • Have approximately 3–5 years of experience in GMP-regulated manufacturing, preferably within biopharmaceutical production.
  • Have a solid understanding of mammalian cell culture processes, from thaw to harvest.
  • Have practical experience with upstream manufacturing equipment and processes, preferably in a GMP-regulated biopharmaceutical environment.
  • Be familiar with GMP requirements, aseptic practices, and accurate production documentation.
  • Be able to independently execute manufacturing activities and contribute to solving operational challenges.
  • Be fluent in written and spoken English.

Responsibilities

  • Prepare media and perform aseptic handling of mammalian cell cultures in a laminar airflow (LAF) bench.
  • Set up single-use manufacturing equipment, including wave rockers and bioreactors ranging from 200 L to 2,000 L.
  • Perform daily sampling of cell cultures, feed additions, harvest, and clarification activities.
  • Ensure accurate and timely GMP documentation and compliance with approved procedures and aseptic practices.
  • Support troubleshooting, deviation investigations, and continuous improvement activities.
  • Take ownership of training and technical qualifications while sharing knowledge and providing practical guidance to colleagues when relevant.

Desired Qualifications

  • Have an educational background as a Process Operator, Process Technologist, Biotechnology Technician, or an equivalent relevant technical qualification.

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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