QA Professional in Aseptic Manufacturing QA (Maternity Cover)

Do you want to use your strong quality mind-set and great interpersonal skills to make a difference within QA? Are you eager to play an important role in ensuring the quality and safety of our products?
 

If so, then read on and apply today for a life-changing career! 

The position
In this role, your key responsibility is, together with your colleagues, to ensure that our documentation is following internal and external requirements. You will do this by reviewing core documents from the aseptic production along with documentation for the supporting processes such as environmental monitoring and utility.  

You could also expect the following:

• Participating in QA oversight as our department is present in the production every day
• Playing a central role where you need to make decisions and set directions for quality

We have a positive working environment with a desire and a will to solve challenges through open and honest dialogue. We work together as a team because we ensure collaboration across competences and take care of each other. 
 

Qualifications
To succeed in this role, you have: 

• Master´s degree in Pharmacy or corresponding education (for example MSc. Chem Eng or MSc. Biology)
• Knowledge about GMP
• Passion for quality, problem solving and LEAN
• Solution-oriented approach
• Fluency in Danish and English
• A proactive mindset, with the ability to anticipate challenges and take initiative

It will be an advantage if you have experience with QA, batch review, or aseptic production.

As a person you are open, honest, forthcoming, and inclusive regarding your colleagues. You enjoy working in a dynamic environment where you take responsibility and take action. You are keen to acquire professional competencies and learn the tricks of the trade. You dare to challenge us in our way of working and has a desire to take initiative as well as being responsible for your own learning.

About the Department
Aseptic Manufacturing (AM) QA Site BA is a department, consisting of approx. 60 dedicated and engaged employees situated in Bagsværd.  Our department ensures a high level of quality in close cooperation with our stakeholders. 

Our responsibility is to assure product quality and regulatory compliance by defining quality requirements, perform quality oversight and by approving quality documents such as procedures, change request and batch- & validation documents. We participate in systematic problem solving and approve deviations. The department is furthermore responsible for assuring the quality of implementation of new equipment and new products in the production facility.
 

Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We're inspired by life in all its forms and shapes, ups and downs, opportunities, and challenges. For employees at Novo Nordisk, life means many things - from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we're all here - to ensure that people can lead a life independent of chronic disease.

Contact
For further information contact Bulut Bulduk at +45 34 48 65 95.
 

Deadline
18 December 2024

To ensure an efficient and fair process, please refrain from including a photo of yourself 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.