Test & Verification Engineer- Medical Devices
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Hillerød
Are you passionate about test & verification engineering? Are you ready to ensure our medical device development projects meet quality standards, operate safely, and comply with regulatory requirements? Would you like to be part of developing the next generation of medical devices for a variety of chronic diseases, and to find even simpler and better test solutions for the future? Then this is your opportunity to use your engineering background to bring medical devices from design to the market. Apply now. Together we bring life-changing innovation. The position
The main responsibilities are to: Lead and manage test projects: define and manage requirements, plan and design verification activities, coordinate and delegate deliverables, and facilitate solutions to mitigate project risks. Drive design verification activities and author test protocols and reports, covering explorative testing, design verification tests, and stability tests. Own an area of expertise, such as a certain test process or specific test cases, and ensure the training of other test engineers in that area. Identify improvement opportunities and drive initiatives to develop our test procedures and programmes to become even better suited for their purpose. Actively share knowledge with the team and stakeholders. You will collaborate with the project teams and use your interpersonal skills to challenge the status quo while focusing on solutions and opportunities. Furthermore, engage in and contribute to a continuous high professional passion and engagement within the test engineering team.
Qualifications We believe the ideal candidate for the position meets the following requirements: An academic degree in Engineering (e.g. mechanical, biomedical) or similar. Minimum 2 years of experience working with test planning, design control/verification, data analysis and reporting, or similar transferable experience within the medical device or other industries. Experience in driving projects or initiatives independently. Proficiency in both written and spoken English. It is an advantage if you have: Experience in medical device development, design control processes for medical devices, or development of drug-device combination products. Acquired knowledge of test standards, equipment and/or method validations and how to navigate in a GMP-regulated environment. Proven record of driving process improvements or training others. As a person, you are proactive, have a ‘can do’ attitude, and drive problem-solving. In your work, you maintain a good overview while ensuring that important details are in place. You contribute to a positive work atmosphere, and you have a track record of successful collaboration towards realising shared objectives. You have an analytical mindset and can easily navigate in the intersection between data, people and processes. About the department
You will join the Experiments & Design Verification department, situated in Devices and Delivery Solutions (DDS), a business unit within the global Development organisation located in Hillerød in the greater Copenhagen area with state-of-the-art R&D facilities. DDS has the mandate and responsibility to innovate and develop the most innovative medical devices for the entire portfolio of Novo Nordisk’s pharmaceutical products. In DDS, highly skilled colleagues within engineering, project management, and technical functions spanning across all competences work together to deliver on a diverse portfolio of drug/combination product and device projects. In Experiments & Design Verification, we are responsible for explorative testing, development of test methods and design verification testing of injection devices and new connected and innovative solutions for drug delivery. Our work is a key part of the device development process, we collaborate with stakeholders across the organisation, and we strive for excellence in everything we do. You will get +50 passionate department colleagues with different international backgrounds, including test engineers, method validation engineers, laboratory technicians and specialists. We are helpful and supporting colleagues, eager to support Novo Nordisk drug-project portfolio, accountable towards timelines, and we take pride in promoting a constructive and collaborative learning culture, challenging your ideas and providing highly competent sparring. Working at Novo Nordisk . At Novo Nordisk, we don't wait for change. We drive it. We're 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're all working to move the needle on patient care. Contact
For further information, please contact Chiara Canali +45 30759515. Deadline
2 January 2024. Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified. 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.
The main responsibilities are to:
Qualifications We believe the ideal candidate for the position meets the following requirements:
You will join the Experiments & Design Verification department, situated in Devices and Delivery Solutions (DDS), a business unit within the global Development organisation located in Hillerød in the greater Copenhagen area with state-of-the-art R&D facilities. DDS has the mandate and responsibility to innovate and develop the most innovative medical devices for the entire portfolio of Novo Nordisk’s pharmaceutical products. In DDS, highly skilled colleagues within engineering, project management, and technical functions spanning across all competences work together to deliver on a diverse portfolio of drug/combination product and device projects. In Experiments & Design Verification, we are responsible for explorative testing, development of test methods and design verification testing of injection devices and new connected and innovative solutions for drug delivery. Our work is a key part of the device development process, we collaborate with stakeholders across the organisation, and we strive for excellence in everything we do. You will get +50 passionate department colleagues with different international backgrounds, including test engineers, method validation engineers, laboratory technicians and specialists. We are helpful and supporting colleagues, eager to support Novo Nordisk drug-project portfolio, accountable towards timelines, and we take pride in promoting a constructive and collaborative learning culture, challenging your ideas and providing highly competent sparring. Working at Novo Nordisk . At Novo Nordisk, we don't wait for change. We drive it. We're 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're all working to move the needle on patient care. Contact
For further information, please contact Chiara Canali +45 30759515. Deadline
2 January 2024. Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified. 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.
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 12.12.2023, 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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- Hillerød
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