Quality & Compliance Partner

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Bagsværd

Can you see yourself as the go-to expert behind quality, ensuring the highest standards for patients where you set the direction? Are you motivated by challenges and working in a dynamic and diverse environment? Do you have strong interpersonal skills to navigate in a complex stakeholder landscape? As our new Quality & Compliance Partner, you will have the opportunity to make a significant impact on quality and quality processes for our whole Contract Manufacturing, Sourcing & Devices (CSD) area. Don’t hesitate to join us - apply today and be the one to set the direction for quality in CSD, ensuring highest quality for patients in a changing and challenging environment! The Position As Quality & Compliance partner, you will represent CSD across Novo Nordisk Quality and be responsible for ensuring a high level of quality and regulatory compliance in CSD. You will provide quality direction and overseeing adherence to our Quality Management System (QMS), to meet applicable regulations and evolving business needs, while maintaining our QMS. You will work in an exciting and dynamic environment where you can provide support across the organisation and offer expert advice on related quality issues to the team members, and across teams in Business Support, other business stakeholders, projects and strategic initiatives, Line of Business (LOB) and Quality Assurance (QA), as necessary. You will have the opportunity to influence and set the direction for quality processes across the organization.
Your main responsibilities include:
  • Driving continuous improvement of processes to ensure quality is maintained while efficiency and value-adding is optimized
  • Acting as Area Process Manager being part of Corporate Process Groups representing CSD in QMS processes such as: Quality Management Review (QMR) and Process Management
  • Providing support to all relevant process roles on process management of processes CSD has ownership, or are represented
  • Liaising with CSD QA and Head of Unit to ensure transparent and timely communication/escalation of quality & compliance issues
  • Coordinate QMR (Quality Management Review) on a Vice President (VP) /Corporate Vice President (CVP) level, being responsible for SVP QMR level
  • Preparing and compiling data analyses and trend data; suggesting improvements based on respective data analyses for QMR
  • The primary work location is in Bagsværd, Denmark, with an expectation of occasional work at various sites in Denmark.
    Qualifications To succeed in this role, we imagine you:
  • Hold a B.Sc or Master degree in Pharmacy, Chemistry, or other scientific discipline, complemented by at least 5 years of practical experience in quality systems and quality processes
  • Feel comfortable engaging with stakeholders across all organizational levels
  • Possess robust communication and facilitation skills
  • Display strong analytical capabilities
  • Are passionate about translating quality requirements into actions and being active on the shopfloor
  • We expect you to have a good business understanding, you are structured and have the ability to prioritize among several key tasks ensuring timely deliverables. It would be an advantage with experience handling and preparing an SVP QMR as well as project management and production experience. As a person, you are characterized by your strong motivation for ensuring the highest quality to patients, and in-depth quality mindset. You possess a strong ability to connect with people and promote a strong stakeholder engagement. Furthermore, your analytical skills stand, coupled with your unwavering passion for translating data into solid recommendations and actions. You thrive by working independently, in a dynamic, multicultural environment and cultivate a cooperative, optimistic atmosphere where people are valued and where decisions are made in a transparent manner.
    About the department You will join SVP area CSD that is responsible for CSD across all product portfolios, external contributors, and on behalf of Product Supply, Quality & IT (PSQIT). This includes strategic sourcing and sourcing operations, manufacturing and development of devices and needles, management of all contract manufacturers, and local manufacturing. You will be part of a small but growing team of SVP Partners within Environment, Health & Saftety and cLEAN as well as 4 Lean Specialists, centrally located, that are working together to reinforce Lean knowledge and mindset across CSD. Working at Novo Nordisk
    Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 60,000 employees. Together, we go further. Together, we’re life changing. Contact
    For further information, please contact Mads Wørmer, Director for Strategy & Business Development, at +45-30794131. Deadline
    2 January 2024. Please note that applications will be reviewed, and interviews will be scheduled on an ongoing basis. Therefore, 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 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 Bagsværd.

    Jobbet er oprettet på vores service den 8.12.2023, 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.
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