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Novo Nordisk A/S in Bagsværd, Denmark, is seeking a Laboratory Technician for the QC Stability 2 team on a two-year fixed-term contract. The role blends laboratory tasks with IT system work to ensure high-quality stability data.
Relocation plans to Future QC are noted, with opportunities to contribute to automation and optimisation of stability processes. You’ll join a department focused on operational stability across the product portfolio, collaborating with CMC, New Product Introduction and
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Department: QC Stability and Reference Materials Location: Bagsvaerd, Denmark
Are you an engaged laboratory technician with a proactive and can-do attitude? Do you enjoy a working day with tasks in the laboratory as well as in IT systems, helping ensure that the quality of our products lives up to strict standards? Would you like to contribute to improving the lives of people living with diabetes and other chronic diseases worldwide? Then you could be our next Laboratory Technician in QC Stability 2 in Bagsværd.
By the end of 2028, the department expects to relocate together with the QC laboratories to Future QC in Hillerød.
You will join us on a two-year fixed-term contract, with the opportunity to contribute to an evolving area and help shape the way we work with stability activities.
What you’ll bring
To succeed in this role, you have:
On a personal level, you have a positive can-do attitude and thrive in a fast-paced and changing environment. We expect that you have a problem-solving attitude towards challenges and that you are a team player, ready to jump in and help your colleagues during busy periods, while also being able to work independently on your own tasks.
Your main responsibilities will include:
The laboratory activities involve handling samples and supporting stability activities and do not include wet chemistry.
QC Stability and Reference Materials is a newly established department, created at the end of 2025 to strengthen the way operational stability is handled across the product portfolio, from Diabetes and Obesity to Rare Disease.
The department is responsible for planning, coordinating and executing stability activities in close collaboration with colleagues across CMC, New Product Introduction and Product Life Cycle Management. It consists of approximately 40 colleagues organised into three teams and is currently located in Bagsværd.
You will join QC Stability 2 and work alongside highly engaged and knowledgeable laboratory technicians, collaborating closely with scientists from New Product Introduction and CMC. The team is responsible for the operational handling of stability studies for new drug products in the portfolio and reference materials, with a focus on the journey from CMC to market launch.
You will become part of a department with a strong quality mindset, high ambitions and a practical can-do spirit. The working environment values curiosity, ownership and teamwork, with your contribution directly supporting reliable stability data and high product quality.
The position offers a combination of laboratory and computer-based tasks, giving you variety in your daily work as well as opportunities to contribute to the continued optimisation and automation of stability processes.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.