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AGC Biologics

End-to-end biopharma CDMO for gene therapies

Manufacturing Support Technician

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeHeidelberg, GermanyIn-person

About the Job

Requirements

  • Completed vocational training as a pharmaceutical technician, chemical technician, biological technical assistant, chemical technical assistant, pharmaceutical technical assistant, chemistry or biology laboratory technician, or comparable qualification; alternatively, a technician qualification or bachelor's degree in a suitable field.
  • Applicants with a technical, hands-on, or production-related background may also qualify; willingness to learn and understanding of quality-critical workflows are important.
  • Initial experience in pharmaceutical, biotechnological, or chemical production, or a comparable regulated environment, is advantageous.
  • A basic understanding of GMP-compliant work and documentation is desirable.
  • Ability to work carefully, reliably, and with a quality-conscious approach.
  • Willingness to undertake practical work involving structured material preparation and cross-departmental collaboration.
  • Ability to work as part of a team, take responsibility, and support other areas when needed.
  • Willingness to work a continuous shift system.
  • Good spoken and written German and English skills.

Responsibilities

  • Weigh, prepare, and supply raw materials, consumables, and process components for production lines in accordance with GMP requirements.
  • Manufacture and provide process tubing and support process preparation.
  • Support inventory management for production storage areas and work closely with Production and Supply Chain Management.
  • Create, maintain, and revise controlled documents for Manufacturing Support.
  • Support compliant storage and shipment of cell banks and APIs.
  • Support qualifications, validations, and the handling of quality-related matters, including deviations, change controls, CAPAs, and investigations.
  • Create complete, accurate, and timely GMP-compliant documentation of all activities performed.
  • Contribute to compliance with and continuous improvement of GMP standards and to improvement measures following self-inspections.

Desired Qualifications

  • Initial experience in pharmaceutical, biotechnological, or chemical production, or a comparable regulated environment.
  • A basic understanding of GMP-compliant work and documentation.

About the Company

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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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