Project Manager for Validation

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Are you ready to support and be part of shaping the future of aseptic manufacturing at Novo Nordisk? Are you motivated by validation and ready to change the game together with your team and the production sites around the world? Then this is a unique opportunity to join a team of highly competent professionals and specialists impacting the way we produce diabetes products around the world. The position As Project Manager for Validation in IFP Manufacturing Development, you will become a member of a team of Professionals and Specialists covering all aspects of the aseptic production in Bagsværd . The team is working as a central unit with the main task of ensuring of implementation of standards for our equipment, systems and processes for aseptic production sites all over the world, thus, you will be working closely together with stakeholders both locally and globally. Specifically working as a Validation Project Manager, you will be a part of a very dedicated, dynamic and highly skilled solely focused on ensuring progress of validation concepts in the inspection process across IFP Sites. Your daily tasks will include, but surely not be limited to:
  • Establishing and executing on ambitious project plans, milestones and activities that will ensure meeting if the deadlines.
  • Creation and maintenance of global corporate documents and procedures including guidelines for qualification of equipment.
  • Creation of global documents in collaboration with IFP Sites
  • Participate in a highly important project of introducing new fully automated
  • Responsible for creating a set-up and governance that ensures maintaining the established standards after implementation
    • Besides you will play an important role in the implementation of the new regulations in relation to the update of EU GMP Annex 1 and other external requirements. As the position is supporting globally some travel (20-25 days a year) can be expected. Qualifications To succeed in this role, we expect you to have a solid understanding of project phases and deliverables, and also:
  • A Bachelor's Degree or higher academic education background within science, engineering, pharmacy or similar.
  • 2-5 years of relevant experience in validation (FAT, SAT, IQ, and OQ). Experience with science and risk-based validation approach is preferred.
  • You have extensive knowledge within Computerised Equipment, in a GMP environment and have 4+ years of experience.
  • Experience managing strategic projects in a global organisation and context. It is advantageous if you have success in creating sustainable solutions for strategic projects and/or initiatives after implementation
  • Strong communication skills with the ability of building relations with stakeholders and create collaboration in a global environment.
  • Fluency in spoken and written English
    • As a person you hold a strong quality mindset and ability to enforce it in a pragmatic way. You are self-driven and independent with a high sense of responsibility, but you also enjoy working in a dynamic environment in which managing multiple tasks simultaneously is a must. You are capable to set direction and drive results independently as you are structured, detail-oriented, curious, good at planning and able to challenge. We will set the scene in a motivating environment with direct impact globally and a close collaboration with very experienced colleagues willing to help you develop – you decide how far! About the department In Injectable Finished Products (IFP) we produce high-quality diabetes products fighting diabetes 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 optimisation 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 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 For further information you are welcome to contact Associate Manager Dejan Peter Kuburovic +45 30 75 64 20 Deadline 12 February 2023. 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 23.1.2023, men kan have været deaktiveret og genaktiveret igen.

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