Validation Engineer
- Category:
- Engineering & Technical
Are you driven by a commitment to excellence in engineering quality and reliability? Do you possess the skills to develop and validate innovative test methods? Collaborate with our expert testing & verification team, engage in critical quality documentation, and refine your analytical skills through data-driven approaches. If you’re ready to make an impact, we want you on our dynamic team in Hillerød.
Join us and transform your career while ensuring compliance and excellence in the development of life-changing devices. Apply today and be part of our mission to improve lives worldwide!
The Position
As an Advanced Validation Engineer, you will join a brilliant testing & verification team in Devices & Delivery Solutions at our site in Hillerød. Your focus will be on taking the lead for test method validation, acting as the validation responsible for devices during development. This position is a 1-year maternity cover and an excellent opportunity to join a growing team.
Part of the role entails serving as an SOP editor, who is authoring, correcting, and reviewing department documents in QualityDocs. This role offers a great opportunity to collaborate with relevant test competency centres.
The main tasks will be to:
• Develop and validate test methods for device development projects, including reviewing and approving PS and MRS with a focus on testability and standard requirements.
• Conduct data analysis using applied statistics and support root cause analysis.
• Be technically responsible for test method development and create measurement uncertainty budgets.
• Develop testing competences to enhance device development, including optimising existing test and measurement processes.
• Supporting equipment capabilities, including calibration and validation activities to ensure compliance.
Qualifications
To succeed in this role, you have:
· A bachelor’s or master’s degree in mechanical engineering, control systems engineering, pharmaceutical design and engineering, medical technology, or similar field.
· Experience in validation and qualification of test equipment, and in developing and validating test methods.
· A minimum of 2–3 years of overall industry experience.
· Familiarity with equipment calibration and maintenance and knowledge of measurement uncertainty budgets.
· Strong skills in data analysis and applied statistics.
· Experience with design verification and validation is considered a plus.
· Experience with SOP editing and document management.
· Full professional proficiency in English (written and spoken). Danish is nice to have.
As a person, you have excellent communication, negotiation and collaboration skills. Having a high degree of flexibility and the ability to work independently is crucial in this role. We're looking for someone who can collaborate closely with test experts across departments.
We will welcome a colleague who has great people skills, a truly analytical mind and a quality mindset.
About the Department
In Devices & Delivery Solutions, we design and develop highly innovative devices and digital therapeutics to benefit patients. Our dynamic, international, and innovative workplace is home to 400 highly skilled professionals who work closely together to develop the next generation of medical devices for people living with serious chronic diseases. Our aim is to further advance our offerings to our patients and their healthcare professionals through new technologies.
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. Novo Nordisk Hillerød
Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.
Contact
For further information, please contact Manager Helen Webb-Thomasen at WBTE@novonordisk.com
Deadline
4 June 2025.
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
