Validation Engineer

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Validation Engineer Are you technically strong and do you dream of being part of Novo Nordisk on a smaller site only 20 min from Copenhagen? Do you want to be a part of providing life-changing medicine to patients with rare diseases? While engaging with many different stakeholders across the organization? Then you might be our new Validation Engineer at our production site in Kirke Værløse. Apply today and start your life-changing career with us! About the department The production site in Kirke Værløse is the part of BRD (Biotech & Rare Disease), which assembles and packages products for patients worldwide. We are a smaller site and are approx. 120 employees, where people know each other and where collaboration across the individual teams is paramount. Here you will become part of a team of 10 technical supporters with different backgrounds and a common goal to ensure a stable development of our assembly and packaging lines. We value good teamwork, a positive atmosphere and all agree that humor is an important part of everyday life. The position You will be a key driver for ensuring our equipment is ready for production within the pharmaceutical industry's requirements, you will be a part of the daily support with expert knowledge for handling incidents, change requests, deviations, and projects. This includes v alidating and documenting changes. This demands a close cooperation with many different stakeholders in relation to planning and coordination of facility activities and release. In other words, you will play a key role in problem solving, document approval, and ensuring that the solutions are in line with industry standards. Your key responsibilities would include:
  • Ensuring that everything runs in accordance with the regulatory requirements of a pharmaceutical production and secure the production lines are in a validated state.
  • Solving complex issues on assembly and packaging lines
  • Implementing automation solutions on both old and new Siemens and Allen-Bradley platforms on assembly and packaging lines.
  • Working closely with operators, technicians, supporters, and Quality Assurance (QA).
  • Data analytics for securing optimized performance of the production lines by having an eye for improvement initiatives, optimization possibilities
    • and cLEAN activities within quality and productivity. Qualifications To succeed in this position, you must have:
  • Proficiency in spoken and written Danish and English
  • A bachelor’s or master’s degree in Mechanical engineering, Production engineering, Marine engineering or similar.
  • A minimum of 2 years of relevant experience with validation techniques, automation, or digitalization on production lines, ideally from the pharmaceutical industry or another highly regulated industry.
    • To thrive in this position, you must enjoy teamwork and proactive collaboration across departments, as well as have an eye for detail and strong quality mindset, as you be handling compliant critical documentation. You thrive in a dynamic environment with daily changes, but your goal is always the same; to ensure stable production and develop our production lines. Contact Should you wish to know more about the position, you are more than welcome to call Associate Manager Niels Peter M. Jordt 30793309 (week 28+29+31) or Per Barkholt 30759428 (week 30). Deadline August 7th 2023 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 Værløse.

    Jobbet er oprettet på vores service den 17.2.2023, men kan have været deaktiveret og genaktiveret igen.

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