Produkt Responsible

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Hillerød

The world is changing fast and so are we. Millions of people depend on our products, which leads to a great demand on maintaining and developing our launched drug delivery systems, and we need you on our journey! Due to an increasing portfolio, we are looking for a new product responsible to join our Durable Device Development team in Hillerød. This is a role for you, If you're seeking a position where you can leverage your skills within design control and stakeholder management to take up responsibility of some of the largest products on the market. The Position In your role as a Product Responsible within Device Development, you will share responsibility for our NovoPen® family with four other colleagues. Your primary tasks include:
  • Driving the work in the post-launch phase of our products, striking the right balance between regulatory and internal requirements, as well as ensuring effective problem solving in collaboration with a wide range of stakeholders.
  • The identification, initiation, coordination, simplification, and execution of device documentation initiatives e.g., mechanical design, requirements engineering, design verification and safety risk management.
  • As a member of the team, to contribute to the continuous improvement of our everyday work as well as process improvement initiatives.
    • The position may occasionally require oversea travel. Qualifications To be considered for this position, we expect you to:
  • Hold a master’s degree in engineering, biomechanics, science, manufacturing, or any other relevant field.
  • Have at least 3 years of experience working with compliance and documentation obtained within a regulated industry (medical devices, pharmaceutical, food, aviation, automotive).
  • It is an advantage if you have experience working with Design Control.
  • Be fluent in English, both spoken and written.
  • Possess the ability to manage and drive several tasks simultaneously and take a methodical approach to your work.
  • Have strong networking and stakeholder management skills, which allow you to set direction, drive performance and ensure quality and speed in a complex stakeholder environment, often with diverging interests.
    • On a personal level, you are:
  • driven by the outlook of being the one person that our stakeholders turn to for product related decisions. You tackle challenges with both determination and a calm, analytical approach.
  • You enjoy working independently both in critical situations as well as in development and maintenance projects with longer duration, and you know how to use your colleague’s expertise for optimal results.
  • You are well-structured and have a systematic way of working, take ownership, seeking simple and effective solutions within the complexity that surrounds a medical device and design control.
  • Lastly, you bring a can-do attitude and a healthy sense of humour to your work, even when the pressure is on.
    • About the Department The position is in Durable Device Development which is part of Device & Manufacturing Development (DMD). Durable Device Development holds the design responsibility for all Durable Novo Nordisk’s medical devices and is the link between Device R&D and production. Our deliverables have direct impact on our ability to deliver to the market, on patient safety, and on compliance with the requirements of the authorities. Working at Novo Nordisk At Novo Nordisk, we do not wait for change. We drive it. We are a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we are all working to move the needle on patient care. Contact For further information about the position please contact Senior Manager Rune Sandvei Skotte +45 34483203. Deadline 15 November 2023, but applications are reviewed at an ongoing basis, so to maximize your chances, kindly submit your application as soon as possible. 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.


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    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Hillerød.

    Jobbet er oprettet på vores service den 2.11.2023, men kan have været deaktiveret og genaktiveret igen.

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