Project Manager for Investment Projects

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Kalundborg

Do you have a scientific background and a strong track record managing complex projects? Do you get motivated by driving investment projects the benefit of millions of insulin-patients worldwide? If so, we can offer you a rarely posted position, where strategy and execution come together, and where you can be a part of changing the lives of millions of people living with diabetes – now and in the future. About the department
As we are growing, we are looking for a Project Manager to join our Projects department in IM1 (Insulin Manufacturing 1), which is part of rapidly growing PS API area (Product Supply Active Pharmaceutical Ingredient). IM1 is a production area, with a total of 600 employees in Kalundborg, where we produce our newest GLP-1 products. You will become a part of a high performing Project Management Office (PMO) team that consists of project managers, project assistants, engineers, and technical professionals. Together we are responsible for execution of investment projects, in a complex, constantly changing and highly regulated pharmaceutical area. Our purpose is to make a change in IM1, by driving small and large-scale projects that improves quality of facility and processes and increase our production capacity.

In the PMO team – and the department as a whole – we are proud about our balance between ambitious goals, working hard and maintaining a healthy and fun approach to our tasks. You will be joining an effective, skilled, and inclusive team, where you will never be alone with the hard challenges or in celebrating your victories.
The Job
As Project Manager, you will be responsible for driving investment projects in a factory and by that have a high impact on our production area IM1 and whole PS API.

Your main responsibilities will be:
• Drive both small and large strategic investment projects from initial idea to implementation and handover.
• Conduct business cases to estimate project potential and drive the projects from start to end to ensure projects are implemented, anchored within line of business and that results are harvested.
• Inspire and motivate the project team to deliver excellent results by ensuring clear project scope and timelines.
• Manage the staffing of our project organization with relevant competencies from consultancy firms.
• Identify and manage risk as the project progresses.

You will most often be responsible for one project at the time and work with stakeholders across the organisation at all levels. The level of complexity in the projects will depend on your competencies and abilities.

Qualifications
• You preferably have a master’s degree or bachelor in a relevant field, e.g. natural science, pharmacy, biology, engineering or similar
• You preferably have at 3-5 years’ experience from working in a medical production, preferably from API production or finished products.
• You ideally have a solid understanding of process equipment, automation and working in a GMP regulated environment.
• You ideally have profound insight into systematic problem solving.
• Lastly, you are proficient in both written and spoken English.

On a personal level, you are a self-starter who thrives with driving tasks independently. You have excellent analytical, planning and organization-skills, which enable you to continuously set direction, keep an overview of the state of progress and prioritize accordingly. With your strong logical ability, you succeed in transforming complex information from the scoping phase to execution and completion.

You have strong leadership skills and a proven ability to network, build trust in your relationships and get commitment form internal and external stakeholders. Furthermore, you have excellent communication skills with the ability to create clear and high-quality presentation materials. We are looking for several new colleagues to the department, so please don’t hesitate to apply if this job sparks your motivation even though you might not meet all the criteria. We will make sure to consider your resume for all our open positions.
Contact
For further information, please call Joakim Herløv 30799063

Deadline
6th of August 2023 and interviews will be conducted on an ongoing basis. You don’t 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 to 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 Kalundborg.

Jobbet er oprettet på vores service den 12.7.2023, 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.
  • Øvrige
  • Kalundborg

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