Injection Moulding Engineer

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Hillerød

Are you a seasoned injection moulding expert looking to apply your technical subject matter knowledge to develop state-of-the-art manufacturing solutions for medical devices? Would you love to be part of Novo Nordisk’s growing journey and support the ramp up to full scale production – and daily operations? Then look no further! Take this rare opportunity and join our Device Manufacturing & Sourcing II (DMS II) department. The position As Injection Moulding Engineer, you will be responsible for the injection moulding tools used to produce plastic device components at our Contract Manufacturing Organisations (CMOs). You play a crucial role along the journey from concept development to full scale operation. You 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 will be the process owner who is responsible for ensuring flawless, safe, and compliant operation of the different tools running around the world. Some of your main focus include:
  • Ordering, commissioning, and validation of new moulding tools
  • Supporting the operation at the contract manufacture with a focus on continuously improvement of processes and mould performance to ensure that we can manufacture quality components in an effective way
  • Involvement in deviation handling which includes root-cause investigation and provide solutions to the issues and implementation of preventive measures
  • Driving different types of technical projects as well as sharing best practice to improve our standards of working (i.e. working in a LEAN way)
  • Participating in requirement definition, concept design of new equipment, design reviews and acceptance testing, including review and approval of relevant documents
  • Initiating and driving improvement initiatives as well as facilitating technology transfer to Contract Manufacturing Organisations
    • The position is located Hillerød/Greater Copenhagen area. You should also expect international travels to equipment vendors and CMO's. Qualifications To be considered for this position, we imagine you:
  • Hold at least a Bachelor’s degree in Engineering or any other related field
  • Have a previous work experience with injection moulding, ideally obtained within a manufacturing development and/or GMP production of medical devices, including process validation
  • Are self-driven, proactive with a high degree of responsibility and possess a high-quality mindset
  • Demonstrate strong stakeholder management skills and the ability to communicate clearly
  • 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 [xxxxx] 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 andContract Manufacturing Organisations (CMOs). 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. Working at [xxxxx] 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 [xxxxx], 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 Michael Thun Klausen at +[xxxxx]. Deadline 31 March 2024. 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 [xxxxx] 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 7.3.2024, men kan have været deaktiveret og genaktiveret igen.

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