Test System Engineer

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Hillerød

Are you looking for a job where you play a key role in ensuring the quality of Devices before they reach the hands of millions of people living with diabetes and other chronic diseases worldwide? Then we encourage you to keep reading as we are opening a position as Test system Engineer in our Design Verification Laboratory and Costumer Complaint Laboratory in Device Manufacturing Development (DMD). Apply today! The position As Test System Engineer in our laboratories, you will play a key role in the maintenance of systems and equipment in the device laboratory including the qualification of new systems and equipment. This includes being part of the specification of equipment, test methods and data handling and you will be responsible for training of test personnel and regular process confirmation. You will have a variety of tasks including but not limited to:
  • Purchase of new equipment in compliance with standards and novo Nordisk’s Quality Management System (QMS) procedures.
  • Handle change-requests and non-conformities covering the full range of novo Nordisk’s medical device and combination products.
  • Ensure compliance in the Device Laboratory, so we always live up to the requirements from the authorities. Including preparation and implementation of necessary standards, standard operating procedures (SOP’s) and ensuring that we follow the SOP’s covering our functional area and train adequately.
  • The position gives you a great opportunity to develop your skills in close cooperation with external test and equipment suppliers as well as a broad range of internal stakeholders, including colleagues in the department, other global novo Nordisk sites, other test departments in R&D, Quality Assurance (QA) and projects owners in DMD. At novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. Qualifications
    Your experiences include:
  • Degree in Engineering or other highly technical fields as relevant
  • You have gained experience with designing and executing tests, with writing and reviewing scientific documents with high technical complexity
  • Experience/ knowledge with GMP
  • Knowledge of LEAN and project managements tools is desirable
  • Its advantagous if you are familiar with equipment validation and operating/maintaining of IT systems
  • Fluent in spoken and written English
  • On a personal level, you demonstrate excellent interpersonal and communication skills with the ability to build relations and collaborate across interdisciplinary boundaries. You see yourself as being proactive and driven to deliver results in a high paced and dynamic environment with many deadlines. When working with colleagues, you are supportive and able to motivate others to meet targets. About the department Device Manufacturing Development (DMD) is responsible for the manufacturing development of all devices and packaging-related processes. We explore new technologies, including robotics, for future production and operate a production unit for clinical production and process optimisation. We take great pride in our diverse and talented team, where over 700 dedicated employees from more than 48 different nationalities work together to achieve our goals and drive change. The position is a part of the “DVT & CC Support” team in Hillerød and is anchored in the Product control and global support department. You will have 11 new team colleagues, cooperate with Laboratory Technicians, Engineers and Specialists, who are dedicated to deliver test documentation that, ensure the authorities’ approvals of assembled Devices. 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 Christian Dines Milling (Associate Manager, DVT & CC Support) on: +45 3075 7431 Deadline
    13 October 2024 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 20.9.2024, 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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