System Software Engineering Coordinator
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Hillerød
- Engineering
- Hillerød
Would you like to work in an R&D department bringing the most innovative medical device concepts from development candidate to launch readiness? Can you collaborate and work with internal and external stakeholders across research and development, production, quality and regulatory affairs? If yes, you could be the perfect match for our device development team in Novo Nordisk, who are responsible for development, design, functionality and regulatory approval of medical devices. We are busy bringing new products to the market and we therefore need a new colleague to join our team.
About the department
Device R&D is an area within our Global R&D organization. We develop medical devices for self-treatment, supporting all business areas of Novo Nordisk A/S. Device R&D is located at a state-of-the-art R&D facility in Hillerød and has a long and outstanding track-record for developing the best, most innovative and widely-used delivery devices in the world. Device Development is responsible for bringing device projects from mid phases to launch.
The position
You will join a high performing and motivated team in Device R&D responsible for delivering Novo Nordisk’s connected medical devices. The team is an interdisciplinary group of hardware, software and mechanical engineers, and together with your colleagues, you will be responsible for driving the development of device firmware and IoS application software for one of Novo Nordisk’s development projects in the portfolio of Connected devices.
In this position you will be in close collaboration with external partners as well as internal stakeholders. You will furthermore be responsible for delivering software related deliveries requested as support to the launch organization for connected devices.
You will become a key part of the Systems team and participate in driving the product development from requirements to preparation for launch submission to preparation for the post-launch lifecycle preparations.
This position offers a good balance between doing technical software reviews, robustness testing, programming and performing project coordination and stakeholder management within Novo Nordisk in a very skilled development team.
The job may involve ownership of system engineering, risk analysis, problem solving, following up on the testing activities, both in the lab and with end-users, and setting direction for the design in order to be aligned with pharmaceutical requirements as well as other design inputs.
You will be responsible for development tasks including planning and coordination with relevant stakeholders. Your tasks will for example include coordination and contribution to requirement engineering, verification and validation. You will work closely with our outsourcing partner for the technical development. For your tasks, you will be responsible for all phases from gathering input to approval.
Your working day will be dynamic with multiple tasks and many interactions to drive activities forward. Your success will be driven by your contributions to the execution of the project, the quality of your deliverables and your way of engaging with colleagues and stakeholders.
Qualifications
You are a strong team player, but you also enjoy working independently and as a person you thrive in a busy environment. You are energetic, and you are comfortable with taking initiative with a ‘can do’ mind-set, and you bring a healthy common sense and a good sense of humor to your work - even when the pressure is on. You are analytical, structured, demonstrate attention to detail, and have a flair for planning and coordinating. Proficiency in both oral and written English is essential. Finally, you like to document your work.
You hold a technical or scientific degree at master’s degree level or above and you have more than 5 years of experience with development of highly regulated products. You are well organized and have experience with good documentation practice within the medical device industry or related industries with similar regulations. You have experience with hardware and software development processes. Preferably, you have experience as a software developer yourself and you are familiar with medical device regulations and industry standards. You work very independently, and you set directions for your team and the team’s responsibilities.
Working at Novo Nordisk
By being patient-focused, we have achieved a market leading position and we continuously develop our expertise to stay ahead – both as a company and as individuals. Working here means joining a team of highly qualified, ambitious colleagues with a passion to bring better treatments to the people who need them.
Contact
For further information, please contact David Böttcher Bæk på tlf.: +45 3079 2990
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
Information og data
Denne ledige stilling har jobtypen "Softwareudvikler", og befinder sig i kategorien "Informationsteknologi".
Arbejdsstedet er beliggende i Hillerød.
Jobbet er oprettet på vores service den 18.11.2019, 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.
- Softwareudvikler
- Hillerød
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