Process Development Engineer (Specialist)

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Hillerød

Are you an experienced Process Engineer passionate about developing production processes, driving troubleshooting of complex production challenges, and taking responsibility for sharing process knowledge across projects? Do you thrive in engaging with stakeholders across all organizational levels in a challenging environment? Would you like to leverage your expertise to directly support senior management decisions, driving design manufacturing processes to support our production capacity expansion, and be a role model for your colleagues? If you are ready to take on an exciting role, we encourage you to take this rare opportunity and apply for the Process Development Engineer (Specialist) position for pre-filled medical devices (FlexPen and FlexTouch) in our truly international Assembly team within Device Manufacturing Development (DMD). The position As one of our Specialists for pre-filled medical devices (FlexPen and FlexTouch) you will oversee development and implementation projects for new assembly production capacities, for our new and marketed products, across multiple geographical locations. You will become a key member of the project and you will:
  • Be part of driving the development of manufacturing processes and design of equipment. Your responsibility will cover a large spectrum from mechanical engineering to instrumentation of the equipment, and operation of the future lines in the production environment
  • Drive troubleshooting processes to solve complex issues in our production sites globally and be responsible for implementing the consequent improvements
  • Collaborate with various stakeholders, e.g., our Information Technology/Operational Technology (IT/OT) department, production experts, and product designers
  • Engage in development activities of future production lines
  • Take part in driving the standardisation and Lean agendas within production processes for pre-filled devices when implementing multiple lines at different sites to ensure that they conform with our corporate risk-based validation approach
    • In return you can look forward to a rich professional experience with strong collaboration with multiple stakeholders from Corporate to local sites, R&D, Production, Suppliers, Quality Assurance (QA) and other specialists in multiple domains. You will also have the opportunity to travel to our production sites or vendors throughout the world. Qualifications To be considered for this position, we imagine you:
  • Hold a master degree in process engineering, pharmacy, or any other relevant field
  • Have a minimum of 6 years of experience as Process Engineer within a regulated industry (pharmaceutical, medical devices or food industries for example)
  • Possess a good understanding of science and technical aspects of the manufacturing processes
  • Are fond of innovation and have a Lean mindset or experience
  • Are fluent in English (both written and spoken) and experienced with MS Office 365, Teams, e-TIMS and other relevant software solutions
    • It would be considered as an advantage if you have a previous experience within medical device development. 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. As an innovative thinker, you are willing to act as lead in our lean activities and to challenge the status quo. Patience, strong communicative skills, and stellar stakeholder management skills will help you deal with the local sites and their practices. It is essential that you are a true team-player at heart: you like to collaborate with colleagues and stakeholders in order to achieve common goals. As a specialist, it is also expected that you will act as a role model for your highly skilled colleagues and that you are ready to support the people around you. About the department You will join Device Manufacturing Development (DMD) and the Assembly department. We are a key function, bridging Device R&D to production. We are involved in the development of new devices, and responsible of the development and implementation of manufacturing capacity worldwide for new and marketed products. We have an end-to-end presence from product development to production implementation and support. We are engaged in numerous complex and strategic projects for Novo Nordisk, impacting the company ability to deliver product to the patients, compliance, and licence to operate, as well as establishment of the factory of the future globally. Our department located in Hillerød includes more than 65 highly engaged skilled professionals including project managers, specialists, validation – and process engineers as well as science experts. We are collaborating with multiple stakeholders and striving for excellence in project execution, science engineering, innovation, and technology. 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, contact Silja Kej Diemer at [email protected]. Deadline 28 January 2024. 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.


    Information og data

    Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".

    Arbejdsstedet er beliggende i Hillerød.

    Jobbet er oprettet på vores service den 21.12.2023, men kan have været deaktiveret og genaktiveret igen.

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