QA Professional in Aseptic production

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:

• Approving deviations 
• 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 similar
• At least 1 year of experience in aseptic production
• Knowledge about GMP
• Passion for quality, problem solving and LEAN
• Solution-oriented approach
• Fluency in Danish and English

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 act. 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
Injectable Finished Products (IFP) 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
At Novo Nordisk, we always strive for excellence and continuously develop our expertise to stay ahead - both as a company and as individuals.  We believe that innovation and creativity thrive in a healthy and engaging working environment. Therefore, we give you the opportunity to bring your personal ambition and passion to work to improve the quality of life of the patients.

Contact
For further information, please contact Associate Quality Assurance Manager Bulut Bulduk at bbld@novonordisk.com

Deadline
2 May 2024. Note that applications will be reviewed on an ongoing basis and the position will be closed when we find the right candidate.
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.