Senior QA Professional

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Are you a highly motivated, solution oriented and self-confident individual with a pas-sion for working with Quality Assurance in a large organization? Can you transform
requirements from the authorities into simple and compliant solutions that are under-standable for our stakeholders globally.
If so, then this exciting job might be your next position! Apply today and join us for a life-changing career! The Position
As Senior Quality Assurance professional within Distribution QA, you will be responsible for imple-menting new external suppliers, such as transport suppliers and temperature logger suppliers. In this role, you will be responsible for ensuring compliance, product quality and patient safety in our daily operations, and offer QA support and GMP/GDP guid-ance internally to Supply Chain Quality Assurance (SCQA).
This position requires a strong quality mindset and a solid process and business un-derstanding.
You will have the following responsibilities:
  • Ensuring Good Manufacturing Practice (GMP) & Good Distribution Practice (GDP) compliance at Novo Nordisk external transport suppliers.
  • Reviewing and approving transport deviations and transport validation.
  • Developing and implementing quality assurance strategies.
  • Continuously securing that NN external transport suppliers operate with the right and optimal quality level. This includes their Quality Management system, licenses/certificates, etc.
  • Writing, reviewing, and approving quality related documents, such as Quality Agreements, etc.
  • Perform QA present with NN external transport suppliers. Participate in relevant audits with external suppliers and internally in Novo Nordisk.
  • Qualifications
    To be successful in this role you:
  • Hold an academic degree in e.g., supply chain, logistics, chemistry, biology, engineering, pharmacy, or similar.
  • Have at least 3 years of relevant experience either within quality assurance or supply chain/distribution.
  • Have worked with supplier handling, preferably in relation to quality processes.
  • Have several years’ of validation experience in roles within supply chain and/ or the pharmaceutical industry, preferably in relation to IT validation/ QA.
  • Fluent in English both written and spoken.
  • Have knowledge of both GMP and GDP requirements.
  • On a personal level you are ambitious, curious, proactive and have a great interest in developing yourself and people in your network. Your attitude is service minded, inde-pendent with an eye for simplicity and take responsibility for your tasks. Finally, you demonstrate great communication skills, this includes being able to com-municate and collaborate with different nationalities and cultures. About the department
    Supply Chain Quality Assurance (SCQA) is responsible for Quality Assurance of and support to Global Logistics & Distribution (GL&D), including cold chain distribution of Novo Nordisk products worldwide, production planning across the entire Novo Nordisk supply chain, and data management and governance across Novo Nordisk. The de-partment has 26 employees and is growing rapidly.
    In our daily work we work closely together with Global Logistics & Distribution (GL&D), our Line of Business, whom we support in quality matters, are involved in high impact projects, and set quality direction for. You will become part of a team focusing on en-suring the quality level at our external forwarders and logger suppliers. It is a team which have a high level of self-governance, good working relations, are informal and value professional sparring and good humour highly.
    Please note that our office will soon be relocating to a new location in Høje Taastrup. Working at Novo Nordisk
    Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabe-tes, 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 63,000 em-ployees around the world. We recognize the importance of the unique skills and per-spectives 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. Contact
    For further information, please contact Hiring manager Paw Winther Brandt-Kofoed [xxxxx] Deadline
    27 January 2025
    Interviews will be conducted on an ongoing basis, so we encourage you to apply as soon as possible. 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 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 Bagsværd.

    Jobbet er oprettet på vores service den 14.1.2025, 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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