Project Manager for Maintenance

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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 standardisation 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 Maintenance in IFP Manufacturing Development, you will become a member of a team of Professionals and Specialists covering all aspects of the aseptic production. 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 Maintenance Project Manager, you will be a part of a very dedicated, dynamic and highly skilled solely focused on ensuring progress of standardising 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.
  • Establishing and maintaining global spare parts strategy in collaboration with IFP Sites
  • Establishing and maintaining global maintenance strategy in collaboration with IFP Sites
  • Participate in a highly important project of introducing new fully automated inspection lines across our sites.
  • Responsible for creating the right governance to ensure maintaining the established standards after implementation
  • 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 can be expected. 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! Qualifications To succeed in this role we expect you to have:
  • A Bachelor's Degree or higher academic education background within science, engineering, pharmacy or similar
  • A great knowledge within Computerised Equipment and 5+ years of experience working in a GMP regulated environment.
  • It is advantageous if you have success in creating sustainable solutions for strategic projects and/or initiatives after implementation.
  • Experience managing strategic projects in a global organisation and context
  • Strong communication skills with the ability of building relations with stakeholders and create collaboration in a global environment.
  • Fluent in spoken and written English
  • You must thrive in an ever-changing environment where your support and decisions make an impact across different sites and enjoy stakeholder collaboration in a global setting. As we are stronger together you must see yourself as a team player with great ability to create relations and collaboration. We are looking for a professional with a “can-do” attitude where no challenges are too big or too small to handle and a willingness to look for new and improved ways to make our processes even better - changing the game. You must be dedicated about your tasks and value the quality of your work. Furthermore, you must be eager to learn and develop your skills. 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 9 April 2023. Applications will be screened on an ongoing basis, so you are encouraged 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.


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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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