Director, Device Manufacturing Development

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“Being part of a development organization places you right in the middle of a vast network of stakeholders. It gives the opportunity to help them resolve their challenges and fulfil their future needs. It is really cool to understand the needs of production or device development and match them with solutions that are generated through close collaboration with technology and research partners”
This is how Ruud describes his role as Director of Components in Device Manufacturing Development (DMD). As he is moving on to pursue other opportunities internally, we are looking for an innovative and empowering leader with a strong background in developing and producing medical devices to lead our Components department. If you are looking for a collaborative and ambitious environment to lead a team and make a difference in the medical device industry, we encourage you to apply for this exciting opportunity. The position
As the Director of Components, you will lead a team responsible for feeding production experience back to engineers to optimize product design for robustness of production. This is done by communicating purpose and setting a vision towards the future by translating higher level strategies and roadmaps in close collaboration with your stakeholders.
As our new Director you will:
  • Build and develop your teams and align employee skills and behaviors with the desired culture, with a focus on diversity and inclusiveness. Ensure clear roles and responsibilities between teams and employees and define the interfaces towards the rest of the organization. You create a future outlook in terms of resource requirements and ensure that budgets are developed accordingly.
  • Ensure that the manufacturing processes are handed over the running production in a structured way, follow up on production performance on a regular basis and initiating improvement projects if necessary.
  • Drive creativity and innovation into the solutions developed, while making sure that technologies are matured to a level where implementation into regulated production can be done in a robust and scalable manner.
  • Meet with your stakeholders on a regular basis, both in formal governance meetings and informally. You gather feedback and discuss the need for new projects to be initiated based on a variety of business drivers, and you bring them forward in the relevant governance forums.
  • You will report to the Corporate Vice President and represent Components in the DMD Management team, where you contribute to organizational development and strategy discussions.
  • As our new Director you will need to understand the key deliverables of the Department and which inputs and conversion processes are required to obtain them. You will be accountable for ensuring that processes are adhered to and comply with Novo Nordisk's regulatory and quality standards. Continuous improvement of current systems and procedures is imperative, and you will be expected to identify gaps and opportunities for enhancement and take the lead in initiating relevant projects.
    Global travel activity is 5 to 10 days per year. Qualifications To be considered for this position, we expect you to:
  • Hold an academic degree within engineering, or any other relevant field
  • Have relevant work experience in manufacturing development and/or production
  • Be familiar with (GMP) production in a regulated industry
  • Possess at least 5 years of people leadership experience
  • Be fluent in English, both written and spoken
  • It would be considered an advantage if you also have:
  • Experience with manufacturing of metal plastics or components
  • Project Management experience
  • As a person, you are a team player who finds joy in assisting others and sharing knowledge. You maintain a humble approach and are open to listening, learning, and acknowledging your limitations by seeking help or advice. You possess exceptional communication skills, which enable you to establish and maintain strong relationships with stakeholders, as well as to convey complex information in a clear and concise manner. You are adaptable to changes in priorities and organization and demonstrate empathy towards others, taking an interest in your colleagues' well-being.
    About the department
    The Components department is one of seven departments in Device Manufacturing Development (DMD) and consists of 4 teams and 50 employees. They specialize in developing manufacturing processes to produce medical device components, as well as process validation and production of new device components for clinical trials and regulatory submission. They have a diverse project portfolio and are constantly seeking new solutions and emerging technologies.
    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 Anders Nørbygaard, Corporate Vice President Device Manufacturing Development, at +45-30752444.
    Deadline
    May 31st, 2023. 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 4.5.2023, 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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