Product Responsible

CMC & Product Supply

Hillerød, Denmark

 

Step into a pivotal role where innovation meets impact—join Novo Nordisk as a Product Responsible and drive change by shaping the future of medical devices with cutting-edge solutions that balance market demands and patient needs. Here, every decision you make contributes directly to improving lives and redefining the standards of care.

 

Your new role
As a Product Responsible, you will take ownership of one of our device platforms together with a team, driving excellence and effectiveness.

Some of your main tasks include:

Driving post-launch activities for our products, adeptly balancing external market demands and internal requirements. Additionally, you should ensure effective problem-solving in collaboration with a wide range of stakeholders. Providing support for development projects as the platform responsible, enabling a smooth and robust launch and continuous manufacturing of new products.  Identifying and executing development, robustness or compliance initiatives related to mechanical design, requirements engineering, design verification, and safety risk management across a platform. Playing a key role in refining our day-to-day operations and driving forward process improvement initiatives.

 

Your new department

In CMC & Product Supply, we cover the full value chain from drug and device development to marketed Novo Nordisk products. We are more than 30,000 colleagues across the globe with the shared responsibility of scaling molecules, processes, devices, and products, dedicated to supplying life-saving medicines to the patients who need them most.

The Marketed Products & Variants area is a dynamic team of approximately 100 skilled professionals who bridge the gap between Device R&D and production, ensuring the quality and compliance of marketed device designs. Our focus is on maintaining existing products while developing new variants that directly impact patient safety and market delivery. We cultivate a collaborative and growth-oriented culture, where self-driven individuals thrive in an international environment to drive innovation and meaningful change.

 
Your skills & qualifications

We’re looking for a new Product Responsible who will enjoy working in a high-paced, dynamic environment. You’ll bring with you:

PhD or master’s degree in engineering, biomechanics, science, manufacturing, or a related field. Fresh graduate candidates will also be considered. Practical experience in compliance and documentation within a regulated industry, such as medical devices, pharmaceuticals, food, aviation, or automotive. Prior experience with Design Control or medical device development would be advantageous. Exceptional organizational skills, adept at managing both short- and long-term projects with a methodical approach. Strong networking and stakeholder management skills, enabling you to set clear direction, enhance performance, and maintain quality and efficiency. Fluent communication in both spoken and written English.

 

On a personal level, you thrive on being the go-to-person for product related decisions among stakeholders. You are skilled at challenging stakeholders and navigating complex scenarios to find impactful compromises. Whether in critical situations or long-term projects, you excel in independent work, leveraging expert colleagues for optimal outcomes. With a well-structured and systematic way of working, you aim to find simple and effective solutions within the complexity that surrounds medical device design control.

About Site Hillerød

Site Hillerød is an innovative and fast-growing production site. With over 4,000 talented employees, we work together to drive change for people living with serious chronic diseases. The site is located in beautiful natural surroundings, and we offer a diverse array of career paths at all educational levels. Join our vibrant community at Site Hillerød and ramp up your career while we ramp up our production! Get to know us better - visit our Site Hillerød career page.

 

What we offer
There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

 

More information
For further information, please contact Theo Stergiou, Manager at TDSQ@novonordisk.com. 

 

Deadline
17 August 2025 (Applications are reviewed on an ongoing basis and the position may be closed before the deadline.)

Novo Nordisk is not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.

 

 

 

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 

 

We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.