Product 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 Platform Maturity team in Device Development. If you want to use your strong skills within design control and stakeholder management to take up responsibility of some of the largest product on the market, this is the position you are looking for! Apply today!
The Position
As Product Responsible in Device Development, you will have the responsibility of one or more of our medical devices and delivery system platforms.
Some of your main tasks include:
The position may occasionally require oversea travel.
Qualifications
To be considered for this position, we expect you to:
It would be considered as an advantage if you have already worked with Design Control.
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 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 expert colleagues for optimal results. You are well-structured and have a systematic way of working, seeking simple and effective solutions within the complexity that surrounds a medical device and design control.
About the department
The position is in Device Development which is part of Novo Nordisk Device & Manufacturing Development (DMD). Device Development holds the design responsibility for Novo Nordisk’s medical devices and delivery systems and is the link between Device R&D and production.
In Device Development, the main task is to maintain marketed products as well as develop new variants of existing product platforms. 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.
You will join the Platform Maturity team and be working alongside colleagues with various educations and work experience. You can look forward to an exciting job engaging with multiple stakeholders at global and local level.
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 Manager Asger Radisch Bredkjær +45 3077 6994.
Deadline
9 December 2022. Please note that applications will be reviewed, and interviews will be scheduled on an ongoing basis.
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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The Position
As Product Responsible in Device Development, you will have the responsibility of one or more of our medical devices and delivery system platforms.
Some of your main 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, and execution of development and enhancement initiatives related to 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 2 to 5 years of experience working with compliance and documentation obtained within a regulated industry (medical devices, pharmaceutical, food, aviation, automotive…).
- 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.
It would be considered as an advantage if you have already worked with Design Control.
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 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 expert colleagues for optimal results. You are well-structured and have a systematic way of working, seeking simple and effective solutions within the complexity that surrounds a medical device and design control.
About the department
The position is in Device Development which is part of Novo Nordisk Device & Manufacturing Development (DMD). Device Development holds the design responsibility for Novo Nordisk’s medical devices and delivery systems and is the link between Device R&D and production.
In Device Development, the main task is to maintain marketed products as well as develop new variants of existing product platforms. 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.
You will join the Platform Maturity team and be working alongside colleagues with various educations and work experience. You can look forward to an exciting job engaging with multiple stakeholders at global and local level.
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 Manager Asger Radisch Bredkjær +45 3077 6994.
Deadline
9 December 2022. Please note that applications will be reviewed, and interviews will be scheduled on an ongoing basis.
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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Information og data
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 17.11.2022, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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Statistik over udbudte øvrige i Hillerød over tid
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