Do you want to use your strong quality mindset and excellent interpersonal skills to ensure that medical components of the highest quality serve our patients? Are you eager to play an important role in ensuring the quality and safety of devices and combination products used in Novo Nordisk clinical trials?
If so, we have an exciting possibility waiting for you as Moulding and Decoration QA in Device Manufacturing Development QA (DMD QA). Apply now and start a life-changing career!
The position
In this role, you will work as Moulding and Decoration QA covering our moulding processes for components for devices and clinical combination products, and you will be part of a team of 12 engaged and highly skilled QA colleagues. The area we support is the area that is responsible for moulding of components for Novo Nordisk clinical trials run worldwide. We play a crucial role in delivering products at the right time in the right quality to ensure patients enrolled in clinical trials can rely on our company.
Your main responsibilities will be to:
Depending on your level of experience and ability to act across different subject matters, you will contribute to improvement projects both internally with our stakeholders and across the Novo Nordisk Quality organisation.
Qualifications
The most important asset that you can bring to succeed in this job is a well-developed understanding of quality and a natural urge to handle quality issues at the right level, make decisions and follow-up on quality related problems.
To succeed in this role, you:
On a personal level, you are ambitious and ready to take responsibility for building strong competencies within our team and fostering trustful relationships across the organisation. You can use your excellent cooperation skills when you manage your stakeholders to ensure solutions that will meet both requirements and stakeholders’ interests. You 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 35+ 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.
We take pride in our work and are constantly seeking to improve our competencies and processes through a focus on simplicity and collaboration. By joining our team, you will have the chance to make a real difference in the lives of patients through the development and life cycle management of crucial medical devices.
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