Stilling
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Do you have project management experience in a pharmaceutical setting or with implementing requirements for materials in a controlled environment? Are you naturally driven to meet set targets and eager to expand your project execution toolbox, and to drive projects aiming at scaling our quality control laboratory to a global setup? Apply today and become one of the two Project Managers we are looking for to lead our strategic projects.
The position
We are looking to expand our team with several people to
support us reaching our strategic aspirations in Sourcing QC. As a
Project Manager, your primary role entails owning and managing
projects from inception to execution.
The first projects will
be to secure a good incorporation of the newly acquired QC
laboratories around the world to the processes owned by
us.
You can also anticipate being involved in projects
related to GMP, quality improvements, optimization and automation
projects. Some of your key tasks will include:
You will work closely with Chemists, Specialist and other project managers supporting on department level in Sourcing QC, but your activities will also include communicating across all levels and business areas in the organization.
Qualifications
To be considered for this position, we imagine you:
As a person, you are resilient and independent, with excellent
communication and collaboration skills. You are structured and
possess an analytical mindset, effectively prioritizing,
assessing, and driving decisions, as well as mastering timely
follow-up and follow-through. You respect others’ opinions yet can
steer a decision through the team. Finally, you are a strategic
thinker who actively acts on changes that could impact projects.
About the department
You will join Sourcing QC (Quality Control) in Product
Supply, Sourcing Operations. The position is in the QC Support
& Development team, but you will provide support to the entire
department. The department consist of approximately 140 employees,
located in Hillerød.
In Sourcing QC, we are responsible for ensuring the quality of
inbound raw materials and primary packaging materials for Novo
Nordisk (NN) production sites worldwide. We cooperate with a
variety of functions, including development departments,
warehouses, business support functions and QA.
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 about the role, please contact
Senior QC Manager Signe Korsager via e-mail: sgks@novonordisk.com
Deadline
1 June 2025
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.