QA Professional (maternity cover)

at  Novo Nordisk

QA Professional (maternity cover)
Category: Quality
Location:Hillerød, Capital Region of Denmark, DK
Are you motivated by regulatory requirements, automated and digitalized testing processes, setting compliance direction and advise your colleagues across the organisation? Can you picture yourself working in a great team with passion for Quality Assurance and thriving by launching important medical devices and combination products to patients in need? Then you might be the person we are looking for in Device Manufacturing Development (DMD QA) placed in Hillerød for a one-year maternity cover, apply now!

QUALIFICATIONS

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.
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.

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