Technician, QC Stability

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.

Technician, QC Stability

Quality Control at AGC Biologics is growing, and we are excited to offer an opportunity to join our expanding QC Stability team.

Are you seeking new challenges in an international and inspiring work environment? If so, this newly created position as Technician in our QC Stability team within Quality Control (QC) might be the perfect opportunity for you.

At AGC Biologics, we specialize in the development of biopharmaceutical production processes and GMP manufacturing for both clinical trials and commercial distribution. As a contract manufacturing organization, we are consistently focused on delivering a high level of service to our clients.

Structure of QC
Quality Control (QC) is comprised of four main departments: QC Support, QC Bioassay, QC Chemistry, and QC Microbiology, with a total of approximately 190 employees.
QC Stability is part of QC Support, assisting all QC departments as well as other divisions within AGC Biologics. You will join a team of three Technicians and five Scientist.

All QC departments are responsible for supporting the production of new drugs in phases I/II and III, as well as commercial pharmaceuticals. The overarching responsibility of the QC Stability team is being responsible for managing our customer’s stability programs for Drug Substances as well as Drug Products. Furthermore, QC Stability also conducts annual testing of reference materials on request and offers support in freeze-thaw cycle studies of the biopharmaceuticals. All work is conducted under cGMP standards.

Responsibilities and Focus Areas
Are you structured, detail-oriented, adaptable, experienced in handling diverse tasks, and familiar with cGMP? If so, you may be the colleague we are looking for. The QC Stability team is seeking a new member for the newly established technician position, which is a full-time role (37 hours per week).

Your daily work will involve varied tasks, extensive collaboration with your team members, and engagement across the organization.

AGC Biologics has expanded its Copenhagen site in Søborg with an additional production building, and the team now handles tasks in both production facilities.

As a technician, you will be part of a team responsible for a wide range of exciting tasks that will primarily consist of preparing weekly stability pulls, the handling of samples whether it’ll be shipping to external laboratories or delivering them to internal testing teams.
Please note that the QC Stability team does not perform analyses or laboratory testing.

You will join a well-functioning team in an open and informal environment, where no two days are alike. The pace is fast, and there is significant interaction with the rest of the organization. In this newly created position, you will take on multiple functions, ranging from office work and stakeholder support to operational tasks in our two production buildings. Therefore, it will be advantageous if you are service-minded, familiar with cGMP, and comfortable managing multiple roles and tasks in your daily work.

Key Responsibilities Include:

Your Profile
You are naturally outgoing, understand process flows, are cooperative, and possess a strong sense of logistics. It is essential that you thrive in a busy and dynamic environment and can maintain an overview despite a work pace, where you are constantly challenged with numerous tasks throughout the day. You should be service-minded, solution-oriented, collaborative, and enjoy interacting with a variety of colleagues throughout the day.

Since we operate under cGMP standards, you must have the necessary structure and attention to detail to ensure everything is in order. Experience in a similar organizational structure would be an advantage.

If this sounds interesting, you might be the perfect candidate to join our QC Stability team.

What AGC Offers
AGC Biologics provides a dynamic workplace with excellent opportunities to work on diverse tasks and challenges. You will gain insight into and experience with how different departments in a contract manufacturing organization collaborate to achieve success.

AGC Biologics employees support one another to meet deadlines as a team, in a professional work environment that also embraces an informal and humorous approach to daily life. There is great respect for each other and individual differences.

Submit your application as soon as possible, as we review applications on an ongoing basis. Qualified candidates can expect to be invited for interviews before the deadline.

We look forward to hearing from you!

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 and give us a quick Like on !