Quality Supporter

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Hillerød

Quality Supporter in Pilot Operations Would you like to work as Quality Supporter in a highly skilled team who are bringing innovative medical devices from development to launch readiness? Does your mindset include a persistent focus on quality in everything you do, and do you thrive in an organization in constant development? Then you may be the perfect match for Pilot Operations! The position As Quality Supporter your primary responsibility will be:
  • Handling quality activities within the team and across the department.
  • Maintaining and improving work instructions.
  • Handle deviations across the department.
  • Supporting verification and validation process equipment and components.
  • Ensuring compliance in all we do.
    • You will work closely together with our process responsible engineers, skilled technicians, and operators. In a regulated GMP environment documentation of high quality is key and you should be able to balance the different requirements needed for e.g., explorative tests and production to clinical studies. You will play an active role in an everchanging environment where assignments and priorities often change and in cooperation with colleagues in- and outside the department you will be responsible for adapting the quality and compliance level. About the department The unit Device Manufacturing Department (DMD) is a project organisation comprising more than 300 engaged employees who all strive to become the best manufacturing development partner of medical devices. Our dedication is to build superior quality into robust device products suitable for high volume production. DMD Pilot Operations is a flexible development and test facility within DMD that supports device development from early R&D development stages into a stable production to market. You will be part of the Moulding team consisting of 10 engaged and dedicated colleagues, and you will be responsible for quality support in our team as well as across Pilot Operations. In the Moulding Test Centre our focus is to perform explorative tests and optimize and validate injection moulding processes. We service our stakeholders by testing machines, moulds, mould concepts, materials etc. ensuring reproducibility and the optimum of technical, economic, and environmentally sustainable solutions Qualifications
  • You hold a relevant degree within engineering or similar academic background. Knowledge and understanding of the injection moulding process is an advantage.
  • You have knowledge and experience within documentation of quality and compliance in relation to GMP
  • On a personal level, you are known for dedicating yourself to work proactively to solve the tasks at hand.
  • You face challenges with a positive and open mind-set to find the best solution in collaboration with our stakeholders. Furthermore, you can make independent decisions and navigate in a complex regulatory environment.
  • You are fluent in Danish and English (both written and oral) and have excellent communication skills as the job requires you to interact with many different stakeholders.
    • Working at Novo Nordisk In Novo Nordisk, you will be met with trust, interesting challenges and rich opportunities for personal and professional growth. You will be investing your unique skills in an environment focused around the exchange of knowledge, where your talent and experience is valued. We are proud to use our dedication and our capabilities to make a difference for millions of people around the world. Contact
    For further information, please contact Claus Munk Mikkelsen +45 3075 9590.

    Deadline The application deadline is 10. March 2023. Interviews will be held on an ongoing basis. Applications in Danish are also welcome. To ensure a fair and inclusive recruitment process, please refrain from adding a personal photo on 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 22.2.2023, men kan have været deaktiveret og genaktiveret igen.

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