- 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
- 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
QA Professional in Aseptic production - Bagsværd, Danmark - Novo Nordisk A/S
Beskrivelse
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:
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:
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.