Engineers for Packaging Process Development

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Hillerød

Are you an engineer willing to bring your expertise to develop and support our packaging production? Do you have experience in bringing pharmaceutical products from development to production via a broad stakeholder landscape? Would you like to join a truly international team, with great colleagues and having fun while supporting production sites all over the world? Then apply today and join our Packaging Team within Device Manufacturing Development. The position We are expanding our team and are looking for Engineers with focus on Packaging Process and Design and Validation of packaging process equipment. You will have the opportunity to enter projects in the development and implementation phase for packaging lines across our many production sites, impacting both new and established products. As a key member of projects, you will:
  • Contribute to the design of equipment and related packaging processes.
  • Collaborate with Device and Delivery Solutions to ensure design for manufacturability.
  • Be engaged in tests, installation, and validation of packaging equipment on packaging sites around the world.
  • Implement and improve validation processes and methods within the packaging process.
  • Collaborate with our Information Technology/Operational Technology (IT/OT) department, emerging technology journey towards Industry 4.0.
    • You can look forward to a rich and diverse professional experience with strong collaboration with multiple stakeholders from corporate level to local sites, R&D, production, suppliers, Quality Assurance, and other specialists. All from different domains in pharma development and from different regions and cultures. Travelling activities to sites and suppliers are expected (approximately 6 weeks per year). Qualifications To be considered for this position, you:
  • Hold at least a bachelor’s degree in process engineering, mechanical engineering, pharmacy, science, or any other relevant field.
  • Have a minimum of 3 years of relevant experience from a GMP regulated environment.
  • Thrive on innovation and have a LEAN mindset or experience.
  • Possess a good understanding of validation and of technical aspects of the manufacturing processes.
  • are fluent in English (both written and spoken).
    • It would be considered as an advantage if you have a previous experience from pharmaceutical or medical devices industry. Who are you as a person? Although we try not to place people in boxes, there are some traits that we believe will help you thrive in this role. You are ideally well organised, someone who never compromises on quality and have a pragmatic approach in your work. You take initiative and enjoy looking across multiple projects and share best practice in between these. You have strong communication and stakeholder management skills and thrives working in an international landscape. It is essential that you are a true team-player at heart: you like to collaborate with colleagues and stakeholders to achieve common goals. About the department You will join Device Manufacturing Development (DMD) and the Packaging Manufacturing Development team responsible for packaging Novo Nordisk finished products, primarily pen injectors and tablets. We are bridging product development to production, and we are driving development and standardisation of new and smarter packaging processes. Further we are responsible for establishing packaging capacity worldwide for new and marketed products in compliance with our current regulatory requirements and in close interaction with Novo Nordisk global production sites. We have an end-to-end presence from device development to production implementation and support to running production. Our department located in Hillerød includes 30+ highly engaged skilled professionals from project managers, specialists, validation, process, and science experts. We are collaborating with multiple stakeholders and striving for excellence in project execution, science engineering, innovation, and technology. 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 Hans Kristian Rømer Westh at +45 3079 6795. Deadline 1 August 2023. Please note that applications will be reviewed, and interviews will be scheduled on an ongoing basis. 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 6.7.2023, men kan have været deaktiveret og genaktiveret igen.

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