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    Environmental Monitoring Professional - Søborg, Danmark - Novo Nordisk

    Novo Nordisk
    Novo Nordisk Søborg, Danmark

    for 5 dage siden

    Novo Nordisk background
    Beskrivelse
    The position
    Environmental Monitoring is an important part of ensuring aseptic conditions in our production cleanrooms.

    You will play a critical role in ensuring that Novo Nordisk Aseptic Filling Facilities, at our global production sites world-wide operates compliant and efficiently.

    As a department, we both support running production and new projects. We are responsible for the interaction between production processes and interpretation of external (GMP) requirements.
    Additional responsibilities involve supporting our sites in environmental cleanroom monitoring, qualification, aseptic operations, and cleaning/gowning.


    Key responsibilities include:
    Participation in troubleshooting and general support to aseptic production at pharmaceutical sites. Maintenance of global corporate documents and procedures for pharmaceutical production. Support in qualification of technologies and improvements across the organization. Provide support in audits and inspections. You will be cooperating with colleagues from different cultures, different areas of expertise and at different organizational levels.

    You will be working out of Søborg, Denmark, and travel up to 20 days over the course of the year may be required in support of our global facilities.

    Furthermore, there will be plenty of opportunities to take on new responsibilities, growth, and development.


    Qualifications Your experience include:

    A master's degree within Biology, Pharmacy, Engineering, Microbiology or equivalent 5+ years expertise within one or more areas of environmental monitoring of cleanrooms in aseptic production.

    Experience with cleanroom and equipment validation, re-validation. Experience with Aseptic Process Simulation (APS – media fill). Strong analytical and statistical skills. Good understanding in regulatory requirements for Environmental Monitoring in cleanrooms. High sense of quality and experience in handling of Quality Management System documentation. As a person, you are service minded, goal oriented and a strong team player. You are accustomed to and thrive working in a dynamic environment. You can prioritize between many important tasks. You set pride in providing excellent support to colleagues and are fluent in written and spoken English. About the department The Injectable Finished Products (IFP) area produces high-quality products to fight diabetes and obesity worldwide.

    Site Support & Improvements (SSI) is a dynamic department in IFP Manufacturing Support, supporting our global IFP aseptic production sites and setting the direction for new technologies, innovation, and production optimization globally.

    We have a strong focus on making a difference in close collaboration with the IFP aseptic production sites, by implementing novel solutions based on data-driven decisions and in accordance with GMP regulations.

    Working at Novo Nordisk Novo Nordisk is a leading global healthcare company with a -year legacy of driving change to defeat serious chronic diseases.

    Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily.

    All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 65, employees around the world.

    We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them.

    Working at Novo Nordisk, we're working toward something bigger than ourselves, and it's a collective effort. Join us Together, we go further. Together, we're life changing.
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