Novo Nordisk

QA Professional for Medical Devices (1 year maternity cover)

Fuldtid

Permanent

Brennum Park 20k, 3400 Hillerød, Danmark

SE PÅ KORT

ID: 2713959

Indrykket for 6 dage siden

We may have the perfect role for you at QA for Device Manufacturing Development (DMD QA) in Hillerød!

Are you looking for an exciting opportunity to advance your career in Quality Assurance? If you're passionate about ensuring regulatory compliance and advising your colleagues on compliant solutions for medical devices, we want to hear from you! With your eagerness to learn about or your experience in product development and life cycle management, you'll work alongside a team of passionate professionals to launch important medical devices to patients. Don't miss out on this chance to take your career to the next level – apply now!

The position
As our QA professional, you will together with the QA team be responsible for delivering best-in-class Quality Assurance and work with our colleagues in Line-of-Business to ensure highest quality of our device products.

You will be responsible for setting the compliance direction within development projects, during submission and launching to markets world-wide, when we transfer our devices from development to production and during life cycle management of Novo Nordisk’s device products portfolio.

You will get an impact on a broad range of the crucial processes to deliver products to our patients.

You will find solutions through a solid process and business understanding and give proactive advice to our stakeholders to secure we establish simple compliant solutions within processes such as: Design Control, Risk Management, and testing.

You will play an important role in ensuring that we build competent skills in Quality Assurance and have an in-depth understanding of relevant regulatory requirements.

We expect you to be highly motivated to learn about device development and eager top take on tasks with curiosity and a “can-do” attitude.

Qualifications
To be successful in this role, you should have:

A Master's degree in Technology, Engineering, Pharmacy, Chemistry, or a related field.

Experience in the pharmaceutical industry either from production, QA, or QC with up-to-date knowledge of quality and GMP requirements, including design control, Validation, Deviations, Corrective and Preventive actions, Change Control, and Complaints.

Knowledge of medical devices design control, regulations, and standards would be advantageous.

Familiarity with connected medical devices, combination products, and needle-based automated injection systems is also beneficial

Fluency in English – both written and spoken.

Ready to lead and build strong relationships? Bring your excellent cooperation skills and flexible decision-making approach to our team. With an open-minded and positive attitude, you're eager to make a difference and learn. If this sounds like you, but you don't meet all the criteria, contact our hiring manager to see if you're eligible!

About the department
At Device Manufacturing Development (DMD QA), we are a department of 42 highly qualified professionals based at our Hillerød site, with diverse backgrounds and interests. In team Product development QA we are 12 highly skilled professionals waiting for you to join us. We are responsible for ensuring the quality and compliance of all processes in Device Manufacturing Development (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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