Principal Technician
AGC Biologics
Principal Technician
AGC Biologics
End-to-end biopharma CDMO for gene therapies
Temp position – 12 Months | Expected Start: January 1, 2027
Are you an experienced upstream Principal Technician with a solid understanding of mammalian cell culture processes, from thaw to harvest? Do you enjoy taking responsibility for production activities while sharing your experience with colleagues?
At AGC Biologics in Søborg, we are looking for a Principal Technician to join our Mammalian Upstream Manufacturing team for a nine-month maternity cover.
You will become part of a team of eight, including your supervisor, working in a dynamic, GMP-regulated environment where different products and customer requirements call for technical understanding, adaptability, and attention to detail.
About the Job
As a Principal Technician, you will contribute to the execution of mammalian upstream manufacturing processes, ensuring that production activities are performed safely, efficiently, and in compliance with GMP requirements.
The role combines hands-on production work with independent responsibility, technical understanding, and close collaboration with your colleagues.
Your main responsibilities will include:
Who Are We Looking For?
We imagine that you:
Beyond your technical experience, we value colleagues who take ownership of their work, maintain high standards of quality, and contribute positively to the team.
You work in a structured way, adapt to changing production needs, and willingly share your knowledge. You communicate openly and know when to ask for support or escalate an issue rather than compromise quality or compliance.
Employment Period & Working Hours
This is a fixed-term temp position for twelve months, with an expected start date of January 1, 2027, and an expected end date of December 31, 2027.
The position follows a 5-2 day-shift rotation, with working hours from 06:00–17:04.
What We Offer
At AGC Biologics, you will join an international biopharmaceutical manufacturing environment where technical expertise, accountability, quality, and teamwork are central to how we work.
We offer:
Interested?
If you have experience with mammalian upstream manufacturing and are motivated by combining technical responsibility with quality and teamwork, we would like to hear from you.
Please submit your application and CV through our recruitment system. Applications will be reviewed continuously, and we reserve the right to close the job posting once we have found the right candidate.
Who We Are
AGC Biologics is a global Contract Development and Manufacturing Organization with a strong presence in Denmark. From our Søborg site, we develop and manufacture life‑changing advanced biologics for some of the world’s most innovative pharmaceutical companies. Together with our team members across Europe, the U.S., and Japan, we deliver development and manufacturing of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells therapies. Across our global network, we are united by one mission: To work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.
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.
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