Project Manager for Labelling

2 weeks ago


Søborg, Gladsaxe Municipality, Denmark Novo Nordisk AS - VTx Full time

Are you ready to take on impactful projects and drive the implementation of complex regulatory requirements? Do you have a passion for improving processes and setting the direction for labelling coordination? If so, we have an exciting opportunity for you to join our Labelling Coordination department at Novo Nordisk in Søborg, Denmark.

Apply today and be a part of our mission to make a difference in the lives of patients worldwide.

The position
As our new Project Manager for labelling at Novo Nordisk, you will be responsible for implementing complex regulatory requirements for packaging material updates.

Your primary responsibilities will include:

• Lead impactful projects across organizational boundaries

• Ensure assessment of labelling impact for integrating new assets/engagements driven by external innovation

• Set the direction for improving our current labelling processes

• Collaborate with stakeholders to ensure effective engagement and communication

• Use your project management skills to drive process improvement and solve complex problems

Qualifications
The ideal candidate has strong project management skills and a proven track record of solving complex problems in a highly regulated environment, ensuring clear continuous communication and effective engagement with stakeholders.

To be successful in this role, you should have:

• A master's degree in a science-related field, such as engineering, supply chain, or pharmaceuticals.

• A minimum of 5+ years of experience with project management and experience in driving cross-organizational process improvement initiatives within the pharmaceutical industry

• Experience with implementing regulatory requirements

• Knowledge and experience with agile project management, GxP and labelling processes are considered an advantage

About the department
The Labelling Coordination department is a global team with locations in Denmark and India. We are responsible for assessing and planning all launches and lifecycle management updates to our packaging material for products worldwide including artwork and master data activities. Our intercultural, collaborative and supportive atmosphere fosters teamwork and allows us to make a difference in the lives of patients worldwide. We are part of the Global Regulatory Affairs Labelling branch of Novo Nordisk comprising approximately 90 dedicated colleagues from across the world.



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