Mechanical Assembly Process Engineer

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Hillerød

Would you like to use your assembly process expertise to develop state-of-the-art manufacturing solutions which will ensure safe and reliable medical devices? Do you want to be part of our growing journey and support the ramp up to full scale production – or even join daily operations? Then look no further! Take this rare opportunity and join our Device Manufacturing & Sourcing II (DMS II) department as Mechanical Assembly Process Engineer. The position is based in Hillerød and Odense. The position As Mechanical Assembly Process Engineer you will be responsible for the assembly lines in our plant and at our Contract Manufacturing Organisations (CMO’s). These fully automated assembly lines put together the individual components into medical device pre-assemblies. You will play a crucial role along the journey from concept development to full scale operation. You will collaborate closely with project managers and colleagues in device manufacturing development, bringing in valuable insights and requirements from an operational point of view. Upon finalization of the development and validation phase, you could be the process owner who is responsible for ensuring flawless, safe, and compliant operation of the assembly lines running around the world. As such, you will:
  • Give Design for Assembly (DFA) input to the component design from a high-volume assembly perspective, Oversee the procurement, manufacturing, factory acceptance testing and validation of new equipment as part of capacity expansions.
  • Participate in requirement definition, concept design of new equipment, design reviews and acceptance testing (including review and approval of relevant documents) as well as development of training plans and material for operators and technicians.
  • Develop operational procedures and instructions, and service and maintenance plans in close collaboration with equipment suppliers, technicians, and operators.
  • Contribute to validation approach: write test and validation protocols and reports as well as supporting the execution of tests and validation activities.
  • Monitor operational performance of the equipment based on data and ensure that the validated state is maintained, troubleshoot issues.
  • Initiate and drive improvement initiatives, facilitate technology transfer to CMO’s.
    • Qualifications To be considered for this position, we expect you to:
  • Hold at least a Bachelor’s degree in Engineering or any other related field
  • Have assembly process work experience ideally obtained within a manufacturing development and/or GMP production of medical devices
  • Knowledge of process validation
  • Be fluent in English, both written and spoken.
    • As a person, you have an inquisitive nature and can strike the right balance between driving results and looking out for the wellbeing of your colleagues. You are able to structure and simplify complex subject matter and focus on the most essential aspects. You are a quick learner, not afraid to admit knowledge limitations and reach out to people across the organisation. You enjoy working in teams and your communication is crisp, to the point and respectful. About the department Novo Nordisk is significantly increasing its manufacturing capacity across all areas to serve many more patients in the coming years. To this end, a new Device Manufacturing & Sourcing business unit (DMS II) has recently been created to ensure medical device component manufacturing and pre-assembly capacity for future growth. In the years to come, we are focused on establishing a new global manufacturing network consisting of suppliers, Contract Manufacturing Organisations (CMOs) and high-volume manufacturing capacity internally. Our DMS II organisation has just started its growth journey, and this is a unique chance to be part of a start-up environment within a large multinational organisation. In the coming period, a wide range of positions will be posted covering a multitude of fields such as supply chain, engineering, operations, project management, people management, and business administration. 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 Ruud Luijs, Vice President at +45 3075 4866. Deadline 24 September 2023. Please note that applications will be reviewed on an ongoing basis, so we encourage you to apply 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 5.9.2023, men kan have været deaktiveret og genaktiveret igen.

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