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AGC Biologics

End-to-end biopharma CDMO for gene therapies

Senior Laboratory Technician - Quality Control, QC Bioassay

Regulatory & Quality (Life Sciences)Posted on Nov 11
Full-timeCopenhagen, DenmarkNo salary listed

About the Job

Requirements

  • A laboratory technician degree (laborant) is ideal, or a relevant laboratory background with an interest in developing skills in the methods.
  • Fluency in spoken and written English is required.
  • Understanding and experience of current Good Manufacturing Practice (cGMP) are appreciated.
  • A structured approach and the ability to adapt priorities, meet tight deadlines, and maintain quality are important.
  • The ability to collaborate positively within Quality Control and with stakeholders, primarily from manufacturing, is appreciated.

Responsibilities

  • Perform analytical testing of drug substance, drug product and in-process samples.
  • Execute bioanalytical methods, including enzyme-linked immunosorbent assay (ELISA), Octet, quantitative polymerase chain reaction (qPCR) and cell-based assays.
  • Participate in stability programs and validate methods used for phase I/II and phase III/commercial products.
  • Report results, including data processing and setup in laboratory information management systems (LIMS).
  • Participate in method validation studies and troubleshoot methods.
  • Perform stop/go sample testing on time to support the manufacturing facility.
  • Cover daily laboratory work and scheduled weekend shifts, and be available for Stop'n Go on-call phone duties supporting manufacturing activities.

Desired Qualifications

  • Hands-on experience with ELISA.
  • Experience with cell-based assays.

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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