QA Professional in Aseptic production - Bagsværd, Danmark - Novo Nordisk

Beskrivelse

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.