QA Professional - Automated device testing
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Hillerød
Are you motivated by regulatory requirements, automated and digitalized testing processes, setting compliance direction and advice 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.
The position
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.
We expect you to be able to handle situations independently, apply your subject matter knowledge, identify better practice, create improvements to processes, share knowledge and to let your colleagues learn and shine.
Qualifications
It is important that you approach your work with an openminded and positive attitude, want to make a difference and are eager to learn.
About the department
Our department consists of 30 highly qualified employees. We take pride in our work, are located at Site Hillerød and are responsible for assuring quality and compliance of all processes in Device Manufacturing Development (DMD). This includes product maintenance, design control, testing, manufacturing development and manufacturing processes. Both internally in Device Manufacturing Development (DMD), and in the rest of Novo Nordisk we have many key stakeholders due to the nature of the processes. We are constantly improving our competencies and our way of working by focusing on simplicity and good collaboration to be able to deliver the best possible support to the business.
Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities, and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.
Contact
For further information, please contact Associate manager Asger Laurberg Vig +45 3075 2770.
Deadline
5th of January 2023
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.
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The position
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.
- 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
- You will be responsible for setting the compliance direction during development projects, during launching to markets world-wide, when we transfer our devices from development to production and during maintenance of Novo Nordisk’s multiple device products
- You will play an important role in ensuring that we build competent skills in Quality Assurance in all aspects of testing and have an in-depth understanding of relevant regulatory requirements
- You will get an impact on a broad range of the crucial processes to deliver products to our patients
- Together with the QA team you will be responsible for delivering best-in-class Quality Assurance
- 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: Laboratory operations, design verification, customer complaint investigations, batch release testing and design control.
We expect you to be able to handle situations independently, apply your subject matter knowledge, identify better practice, create improvements to processes, share knowledge and to let your colleagues learn and shine.
Qualifications
- A master’s degree within engineering, Medicine and technology, pharmacy, chemistry or similar
- Experience from laboratory activities preferably in the pharmaceutical or Medical Device industry and have worked with quality processes
- 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
- You are well-organised and have a flexible, but firm approach when making decisions
- It is an advantage but not a requirement, that you have worked with medical devices and combination product, as well as has experienced with interpretation of relevant regulatory requirements and standards
- Knowledge and possible experience with automated testing is also considered as an advantage
It is important that you approach your work with an openminded and positive attitude, want to make a difference and are eager to learn.
About the department
Our department consists of 30 highly qualified employees. We take pride in our work, are located at Site Hillerød and are responsible for assuring quality and compliance of all processes in Device Manufacturing Development (DMD). This includes product maintenance, design control, testing, manufacturing development and manufacturing processes. Both internally in Device Manufacturing Development (DMD), and in the rest of Novo Nordisk we have many key stakeholders due to the nature of the processes. We are constantly improving our competencies and our way of working by focusing on simplicity and good collaboration to be able to deliver the best possible support to the business.
Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities, and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.
Contact
For further information, please contact Associate manager Asger Laurberg Vig +45 3075 2770.
Deadline
5th of January 2023
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.
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Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Hillerød.
Jobbet er oprettet på vores service den 9.12.2022, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Hillerød
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Statistik over udbudte jobs som øvrige i Hillerød
Herunder ser du udviklingen i udbudte øvrige i Hillerød over tid. Bemærk at jobs der ikke har en bestemt geografi ikke er medtaget i tabellen. I den første kolonne ser du datoen. I den næste kolonne ser du det samlede antal øvrige.
Se flere statistikker her:
Statistik over udbudte øvrige i Hillerød over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 26. november 2024 | 57 |
| 25. november 2024 | 55 |
| 24. november 2024 | 67 |
| 23. november 2024 | 66 |
| 22. november 2024 | 65 |
| 21. november 2024 | 64 |
| 20. november 2024 | 63 |
| 19. november 2024 | 64 |
| 18. november 2024 | 62 |
| 17. november 2024 | 71 |
| 16. november 2024 | 71 |
| 15. november 2024 | 69 |
| 14. november 2024 | 68 |
| 13. november 2024 | 59 |
| 12. november 2024 | 63 |
| 11. november 2024 | 61 |
| 10. november 2024 | 63 |
| 9. november 2024 | 63 |
| 8. november 2024 | 63 |
| 7. november 2024 | 67 |
| 6. november 2024 | 64 |
| 5. november 2024 | 61 |
| 4. november 2024 | 64 |
| 3. november 2024 | 66 |
| 2. november 2024 | 67 |
| 1. november 2024 | 65 |
| 31. oktober 2024 | 63 |
| 30. oktober 2024 | 61 |
| 29. oktober 2024 | 70 |
| 28. oktober 2024 | 71 |
| 27. oktober 2024 | 74 |