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 to improve patients’ lives by bringing new biopharmaceuticals to market.
At AGC Biologics in Søborg, this purpose becomes reality every day in our manufacturing facility, where biopharmaceutical production processes are transformed into products for clinical studies and the market.
As part of our Downstream Manufacturing team, you will play a hands-on role in the purification of biopharmaceutical proteins. Working in a GMP environment, you will operate purification equipment, execute production processes, and help ensure that every batch is produced and documented according to our quality standards.
If you enjoy working with technical equipment, structured processes, and colleagues who depend on each other to keep production moving, this could be the role for you.
Downstream manufacturing is where the product is purified and prepared for the next stage of the production process.
As a technician, you will be responsible for planning and performing different steps in the protein purification process.
Your work will include setting up production equipment such as SUM systems, columns, filters, and Äkta Ready systems. You will execute processes including HETP, chromatography, Nano filtration, and UF/DF filtration, as well as perform swabbing and sampling.
Documentation is an important part of the role. You will complete and review MPRs and logbooks and help ensure high quality in the batch documentation in close collaboration with QA and QC.
You will also prepare production rooms and systems before and after production and participate in qualification, maintenance, control, and calibration of equipment.
Together with the team, you will be responsible for delivering the product to the filling team.
You will become part of a production area consisting of five production lines producing preclinical, clinical, and commercial products for a wide variety of clients.
The team consists of dedicated technicians and academics who work closely together and collaborate with colleagues across functions including QC, QA, and Development.
Production can be dynamic and fast paced, and flexibility and teamwork are important parts of keeping the processes running and solving challenges together.
We are looking for someone who enjoys hands-on production work and working in a structured GMP environment.
You will preferably bring:
As a person, you are positive and flexible and comfortable taking on new assignments and responsibility. You thrive in a dynamic work environment and can handle unpredictability.
This position operates on a night shift from 20:00 to 07:00.
You should also be prepared to take on overtime during peak production periods.
AGC Biologics is a Contract Development and Manufacturing Organization (CDMO) within the biotech industry. We work with the development of biopharmaceutical production processes and GMP production of biopharmaceutical proteins for both clinical studies and the market.
At AGC, you will have opportunities to work with a wide range of tasks and challenges and gain experience across our different departments. As projects and tasks are planned together within the team, you will also have the opportunity to influence your daily work.
We work in an informal environment where energy, enthusiasm, respect for individual differences, flexibility, and helping each other reach deadlines are important parts of everyday work.
If you have experience with protein purification and want to work hands-on with technologies such as Äkta Ready, chromatography, and filtration in a GMP manufacturing environment, we would be excited to hear from you.
We review applications on an ongoing basis, so please submit your application through our recruitment system.
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.

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 to provide friendly and expert services. We provide world-class development and manufacturing 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, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan.
Visit www.agcbio.com to learn more.