Inspection Supporter

Are you driven by being part of a strong community in a department where we deliver life-saving medicine to patients around the globe? Do you dream about making a true difference? Would you like to help us implement new products, tackle new technology and drive exciting projects, with a focus on continuous optimization?

If so, you might be our new Inspection Supporter to join the team at Site Bagsværd. Read on and apply today!

The Position

As an Inspection Supporter, you will be part of our fantastic and professional team of 22 people who have extensive knowledge of both the process and technical part of our CVT lines. Our most important task is to ensure that only the best quality of our products ends up with the patients by supporting our production, optimize processes, find solutions for challenges and ensure we are in compliance with GMP regulations. Not a single day is the same in our production. Together with other team members, you will handle deviations, write reports, systematic problem solving, update SOP’s, work with projects across departments as well as validation and qualification of equipment.

Right now, we are implementing a new inspection line, and are frontrunner in the machine learning journey on our CVT line. 

In this position there will be a good amount of solving production challenges and projects/implementing new equipment, as well as developing new processes. There will be room to form your own position based on what is interesting for you e.g. if you find it interesting with process group, signal audits and inspection, or machine learning, technology and equipment. The work is done in close collaboration with the rest of the team, where we emphasize unity and engagement in a busy everyday life. We foster a strong team spirit, where we are collaborating daily, lift together and share our successes.

Qualifications

To be a competitive candidate, you should:
• Hold bachelor’s or a master’s degree in engineering or similar.
• Have experience in the production, which is considered an advantage.
• Have a flair for working with processes, deviations, problem-solving, data in Excel, and validations/qualifications.
• Have knowledge of or experience with complying with GMP requirements.
• Be fluent in written and spoken Danish and English. 

We will provide necessary training and can adjust the role depending on your experience.

On a personal level, you have a strong compliance mindset, and like to lead new improvements and tackle challenges in a positive way. Being structured, quality-conscious, and dedicated to work while being able to complete tasks within the deadline is a crucial part of this role.

As a strong communicator, you thrive on working independently and as a team player across departments and the organization. Having a good overview and a sharp analytical sense, being able to cut to the chase and understand the connections between processes, materials, and equipment is key to succeed in this team.

About the department

You will be part of our AM Inspection & Warehouse department, which works with the production of our new products, and where we are currently implementing new production technology. We are about 100 dedicated employees in the department, all of whom have their daily routines at our site in Bagsværd. The department has two production lines that inspect our clinical and marketed insulin products, ensuring that the quality is top-notch before it reaches our patients. Additionally, we are implementing a brand-new inspection machine, not seen elsewhere at Novo Nordisk. We work closely across teams and professional groups to ultimately contribute to the absolute best quality of our product.