Supply Chain Coordinator for Imported Release

Category:  Quality
Location: 

Bagsværd, Capital Region of Denmark, DK

   

Do you want to make a difference within our release supply chain? Are you passionate about cooperation with many stakeholders to improve the business? Are you eager to make continuous improvement and use your passion to work towards simplicity and agility? Then we have just the right job for you, as we are looking for a colleague to coordinate our supply chain for release of products in Aseptic Manufacturing (AM) QA, apply now! 

 

About the department  

Our department consists of approximately 60 dedicated employees being responsible for assuring quality and compliance of diabetes finished products produced in Site Bagsvard. Beside that we have responsibility for release of products produced in Site Bagsvaerd and products imported into EU from our foreign production sites across the world. In close cooperation with our stakeholders, we ensure a high level of quality and have a key function in quality assurance of the production processes. 

 

The department is divided into 4 teams and the open position is in the QA team responsible for release of products imported into EU from our production sites in Brasil, US, France and China.   

 

The position 

The team’s main responsibility is release of products imported into EU from AM production sites worldwide and this involves several international and national stakeholders covering production, QC laboratories and the supply organization. Therefore, stakeholder management is an important part of this position, as the team’s deliveries are highly dependent on a good collaboration.  

 

As a Supply Chain Coordinator, you will be leading and coordinating the release flow for products produced worldwide and imported into EU. You must develop a clear and transparent release flow structure in cooperation with all stakeholders in site and out site Denmark. Tools to ensure common and aligned overview must be implemented and maintained. 

 

Many stakeholders are involved in the flow – production sites, QC, QA Supply chain planning, Warehouses and Affiliates. You will, together with your team colleagues, ensure to build and maintain a close collaboration with the stakeholders and common alignment.  

Simplicity and efficient daily operation are in focus in the department and needs to be further developed.  

 

Qualifications 

To succeed in this role, you: 

  • hold a master’s degree in e.g. Supply Chain Management, Engineering, Business Administration, or within Pharmacy, Chemistry, Microbiology 
  • have a minimum of 3 years of experience working with flows from either production, quality control, quality assurance or supply chain 
  • have preferably gained said experience from the pharmaceutical industry 
  • are fluent in English and preferably in Danish 

 

On a personal level, you have a can-do attitude and proactively strive for higher levels of performance not being afraid of being challenged by peers and employees. You bring a quality mind-set and are able to balance compliance and product quality when making decisions and can stay firm when needed to secure the quality and compliance aspects. You can differentiate your communication depending on the target group and present your arguments in a professional way. 

 

Lastly, you are well organized and create strong results by engaging with your colleagues in taking pride in delivering on your objectives.  

 

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, please contact Christina Grebin Rosenkilde on +45 3079 9624.  

 

Deadline 

26 February 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.