Engineer for process validation

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Hillerød

Are you eager to test and validate new equipment and manufacturing processes to the limits? Do you thrive on teamwork, collaboration and are you able to drive projects and set direction? Would you enjoy going to work every day knowing that your contribution makes a difference? Then join us and become part of something unique – this position will provide you with excellent opportunities for personal and professional development. The position As Engineer for process validation, you will be responsible for planning, executing, and reporting validation activities for our manufacturing processes for medical device components. Some of your main responsibilities include:
  • Leading and contributing to the validation activities of the project, from basic design and establishing User Requirement Specification (URS) to process risk assessment, all the way to Process Validation of the new equipment
  • Creating and executing validation plans, test protocols, test plans and reports based on input from stakeholders to the process in scope
  • Ensuring validation plans, protocols, etc. are followed and that any validation deviation is reported and solved to the root cause
  • Peer review of validation documentation
  • Creating and maintaining validation procedures and templates, in close collaboration with your stakeholders in other parts of the Novo Nordisk organization.
    • As this role involves handling and collaborating with many external stakeholders, travel will be required (up to 20 days a year). Qualifications To be successful in this role, we envision you as someone who:
  • Holds a master’s degree within Engineering, IT with validation focus or any other relevant field
  • Preferably has previous experience within validation of manufacturing processes for medical device components but if you are newly educated and has a desire to work with process validation, don’t hesitate to apply for this position
  • Is ideally familiar with the many requirements within medical device production but if not, we will ensure proper training opportunities for you
  • Is a proficient user of both spoken and written English.
    • We believe that you will thrive in this role if you have strong communication skills, an outgoing personality, and can form as well as maintain relationships across and beyond the organization. You are great at engaging and managing stakeholders, and your direction-setting initiative is rivaled only by your ability to follow through and your keen appreciation of quality. You enjoy sharing your knowledge, providing support for your colleagues when they need it. About the department You will be joining a team of highly skilled colleagues in an international environment within Novo Nordisk Device Manufacturing Development facility in Hillerød. In close collaboration with our suppliers, we are developing the equipment and processes that transform great designs into actual products for our patients, bridging the gap between development departments and the production lines. With a mindset focused on continuous improvement, efficiency and curiosity the success we enjoy are always under further development. We strive to ensure they meet and exceed the expectations of a growing and demanding market. We design all the equipment necessary to perform all the processes involved in manufacturing the metal components for our dosage pen systems - and this is where we need you. In our team, no one gets left behind: we enjoy sharing our knowledge, and we are eager to get to know you and learn from you. We like to keep a casual, informal tone, but we are also deeply passionate about our work and the difference we make in millions of people’s lives. If you appreciate collaboration in a creative and ambitious environment, you will feel at home with us. 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 If you have question regarding the job, you are welcome to call René Bohnstedt Schnack at +45 30 75 92 70. Should you wish to learn more about what it is like working in Novo Nordisk, you can begin here : http://www.novonordisk.com/careers/working-at-novo-nordisk.html Deadline 13th 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.


    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 26.7.2023, men kan have været deaktiveret og genaktiveret igen.

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