Manufacturing Technician Pipeline

4 days ago

Copenhagen, Copenhagen, Denmark AGC Biologics Full time

Manufacturing Technician Pipeline AGC Biologics

Manufacturing Technician Pipeline AGC Biologics

Apply time type Full time posted on Posted 30+ Days Ago time left to apply End Date: March 31, 2025 (30+ days left to apply) job requisition id JR100780

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients' lives by bringing new biopharmaceuticals to market.

Technicians in Manufacturing at AGC Biologics, Copenhagen

Are you interested in working with the latest equipment and technology? Do you have a background in process operations and experience with systems? Do you thrive in a dynamic, fast-paced environment? If so, AGC Biologics could be the right place for you

About AGC Biologics

AGC Biologics A/S is a global Contract Development and Manufacturing Organization (CDMO) within the biotech industry. We specialize in developing biopharmaceutical production processes and GMP production of biopharmaceutical proteins for clinical studies and commercial markets.

Join an International and Agile Organization

At AGC Biologics, you'll have the opportunity to work on a variety of tasks and challenges across different departments. We value teamwork and offer an informal working environment characterized by high energy and enthusiasm. We respect individual differences and help each other meet deadlines as a team.

Job Description

Join our production team, which consists of five production lines that manufacture preclinical, clinical, and commercial products for a diverse range of clients. Our team comprises dedicated professionals, including technicians and academics, who collaborate with various partners, such as QA, QC, and Development.

As a technician, you will be involved in planning and executing different steps in the production process, including protein purification and equipment setup.

Key Responsibilities:

  • Setting up and operating equipment (e.g., SUM systems, columns, filters, Äkta Ready systems)
  • Executing processes such as HETP, chromatography, and filtration (Nano & UF/DF filtration)
  • Sampling and documentation
  • Preparing production rooms and systems before and after production
  • Participating in the qualification, maintenance, control, and calibration of equipment
  • Ensuring high-quality batch documentation in collaboration with QA/QC
  • Supporting the delivery of products to the next stage of production

Areas of Focus

We are looking for technicians in the following main areas:

  • Microbial Production
  • Mammalian Production

Within these main areas, you could be working in one or more of the following sub-areas:

  • Upstream Processing
    • Cultivation of cells
    • Media preparation
    • Bioreactor operation
  • Downstream Processing
    • Protein purification
    • Filtration
    • Chromatography
  • Solution Preparation
    • Buffer preparation
    • Media and solution mixing
    • Sterilization

About You

We imagine that you:

  • Hold a relevant degree in a scientific or technical field
  • Are interested in equipment maintenance and instrumentation
  • Possess strong collaboration and communication skills
  • Are proficient in English (reading, writing, and speaking)
  • Are positive, flexible, and thrive on new assignments and responsibilities.
  • Can handle unpredictability and work effectively in a dynamic environment

It would be an advantage:

  • Having 1+ years of experience in the biopharmaceutical or related industry, preferably in a cGMP environment
  • Have experience with protein purification and chromatography using systems like Äkta Ready or Process

Work Conditions

Our production team operates on rotating shifts, including days, evenings, nights, weekends, and overtime during peak periods. Flexibility in work hours is essential.

We review applications on an ongoing basis, so send in your application today.

Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients' most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com.

Want to keep posted about our growth and learn more about our company? Follow us on LinkedIn and give us a quick Like on Facebook

AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.

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