Senior Quality Responsible for Future QC

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Would you like to be part of an exciting journey to design, build and relocate to our new QC Laboratory, which will secure the needed QC capacity for the future? Are you passionate about the quality and regulatory processes in construction projects, and want to combine this with your project manager skills? Then there is a challenging job opportunity as Senior Quality Responsible in our construction project “Future QC Laboratory”. The position With the responsibility for the Quality work package, you will be part of the project team consisting of a Project Vice President, with the overall responsibility, fellow work package owners, architects, consulting engineers and end users. Together the project team will ensure that our Future QC Laboratory is delivered timely in full GMP Compliance to ensure an effective relocation process with the needed authority approvals obtained as fast as possible. As a Senior Quality Responsible you will be responsible for:
  • Development of the project quality strategy in collaboration with the project team and QA, including authoring and maintaining the Project Quality Masterplan.
  • The schedule for quality activities (for example commissioning, qualification, regulatory, and inspection activities) all the way to §39 approval and the relocation of users into our new laboratory.
  • Progress and follow-up on timely execution of Quality Activities, as well as facilitation of risk and quality workshops.
  • Proactively identify quality challenges and secure the necessary agreements/clarifications with stakeholders such as consulting engineers, end users, QA, regulatory, IT and management.
  • Plan and ensure execution of all activities needed to relocate the departments into our new laboratory.
  • Ensuring that the build and documentation package can pass internal audits and authority inspections.
    • Qualifications Ideally you have the following qualifications:
  • Minimum 3 years of experience from the pharmaceutical industry, and a Master´s degree in Engineering, Pharmacy or corresponding education (for example MSc. Biochemisty).
  • Experience with construction projects in the pharmaceutical industry, as well as the quality processes related to such projects (for example risk assessment, design, qualification /validation and audits).
  • Project Management experience with knowledge about the basic Project Management tools is preferred but not required.
  • Proficiency in English and Danish as we operate in an international company and the position therefore requires.
    • On a personal level you possess good people management skills, strong collaboration skills, the ability to set direction and motivate your colleagues. You have the right quality mindset, dare to challenge our way of working and are known for your ability to identify improvements, as well as taking the lead for driving the implementation of these improvements. About the department The project will build a multi-functional QC laboratory at Novo Nordisk Site Hillerød and be the future workplace for 650 QC collages. Both chemical and microbial QC-laboratories will be established, as well as development laboratories within these areas. When functional the laboratory will deliver analytical support to production units across Novo Nordisk covering products for treatment of diabetes, obesity, rare blood and endocrine disorders. The laboratories will be ready for our ambitious goals for QC Automation & Digitalisation. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact If you want to hear more about the position, contact Jakob Hovalt Mathiassen (Senior Manager) on +45 30792404. Deadline 5 June 2023. We may conduct interviews before the deadline. Therefore, we may take the liberty to close for new applicants before the deadline. 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.


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    Jobbet er oprettet på vores service den 7.10.2022, men kan have været deaktiveret og genaktiveret igen.

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