IT Responsible

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Gentofte

We believe in the detail that our patients deserve the best. We believe in making the complex easy, to create simplicity in our daily tasks. We do that by navigating the rules and regulations, in a highly GxP regulated world, we do it to ensure that our production stay in compliance. Do you have experience in GxP documentation practices? Enjoy and excel in documentation, and are you able to overview the life cycle of productions systems?

If so, then your eye for detail is what we are looking for. Join us today!
About the department
The team ensures IT Compliance for both our aseptic filling departments and our packing facility in Kalundborg, Gentofte and Måløv. The departments are part of the Digital, Data & IT organization in Product Supply (DD&IT PS) Our biopharmaceutical products are characterized by complex processes supported by employees with great professionalism and commitment.

You will be part of an IT Compliance team with 12 people – 4 IT System Managers and 7 IT Responsible. We have offices in Gentofte, Måløv and Kalundborg, but you will primary work out of our office in Måløv and Gentofte.
What’s in it for you?
As our new IT Responsible, you will make sure that the IT part of our production equipment are in compliance primarily for our new facilities.

Additionally, we expect you to:
  • Manage and overview the full life cycle from system development, system maintenance. operations, and compliance
  • Ensure optimal processes according to relevant regulatory authorities (GxP) and take responsibility for documentation for the IT part of automated system and security management for the system
  • Ensure that the systems are compliant with relevant internal SOPs and guidelines as well as external requirements
  • Supervise that appropriate testing is in place ensuring that IT requirements are met
  • Represent the IT part of the systems in connection with audits and inspections
  • Qualifications
    We expect you to have a BSc or MSc in Computer Science, BA, Engineering or other similar fields, preferably with a background in Pharma, Quality.

    Furthermore, you have:
  • Fluent oral & written communication skills in English and Danish
  • Ability to independently make technical documents
  • Preferably, you are knowledgeable within areas such as IT frameworks and system development lifecycles, operation and maintenance of automated systems.

    Bring your questions
    For further information, please reach out to our department Hiring Manager, Esben Wismann Larsen at [email protected]

    Deadline
    30 June 2023

    Note that relevant candidates may be invited for interviews on an ongoing basis before the deadline. Therefore, rather apply today, than tomorrow. 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 Gentofte.

    Jobbet er oprettet på vores service den 6.6.2023, 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.
    • Øvrige
    • Gentofte

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