Denmark Job Openings
Novo Nordisk
QA Professional (maternity cover)
Hillerød
September 12, 2024
We are currently expanding our automated and digitalized testing facilities which are used in our local laboratories as well-as world-wide for release of our innovative products within the devices category. You will be responsible for setting the compliance direction within operations in laboratories as well as testing equipment, methods and IT in digitalised and automated laboratory processes.
Among other key responsibilities, you will:
- be responsible for setting the compliance direction during development projects, market launches world-wide, production activities and their maintenance.
- play an important role in ensuring that we build competent skills in QA in all aspects of testing and have an in-depth understanding of relevant regulatory requirements. impact on a broad range of the crucial processes to deliver products to our patients.
To succeed in this role, you:
- hold master’s degree within engineering, medicine and technology, pharmacy, chemistry or similar, or a bachelor’s degree supported by extensive experience.
- have experience from laboratory or QA activities, within the pharmaceutical or medical device industry.
- preferably have worked with medical devices and combination products.
- preferably have experience with automated testing and validation.
- are fluent in English.
On a personal level, you are ambitious and ready to take on the responsibility in building strong competencies in our team and trustful relations across the organisation. You can use your excellent cooperation skills when you manage your stakeholders to ensure solutions that will meet both requirements and stakeholder’s interests and it is important that you approach your work with an openminded and positive attitude, want to make a difference and are eager to learn.
Finally, you are well-organised and have a flexible, but firm approach when making decisions.
About the department
At DMD QA, we are a team of 42 highly qualified professionals based at our Hillerød site, with diverse backgrounds and interests.
We are responsible for ensuring the quality and compliance of all processes in DMD, including product development and life cycle management, design control, testing, manufacturing development, and manufacturing processes.
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.
For further information, please contact the QA manager Carlos Gonçalves at +45 3079 4194.
29 September 2024
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