QA Professional for Medical Devices (1 year maternity cover)

Job title:

QA Professional for Medical Devices (1 year maternity cover)

Company:

Novo Nordisk

Job description

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Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading…CategorySelect how often (in days) to receive an alert:×Select how often (in days) to receive an alert:QA Professional for Medical Devices (1 year maternity cover)Category: QualityLocation:Hillerød, Capital Region of Denmark, DKWe 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.Working at Novo Nordisk
Novo Nordisk is its people. We know that life is anything but linear, and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing.Contact
For further information, please contact QA manager Jane Frederiksen +45 3079 9796.Deadline
25 September 2024.
You may submit your application in English or in Danish.
We will review applications received on an ongoing basis, so do not hesitate to apply today. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV.
To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

Expected salary

Location

Hillerød, Hovedstaden

Job date

Fri, 13 Sep 2024 01:44:05 GMT

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