Advanced QA Professional of medical devices
Denne stilling er desværre ikke længere ledig.
Se alle ledige stillinger
Hillerød
Are you motivated by quality and regulatory requirements and the opportunity to advise your colleagues on compliant solutions for medical devices? Do you have experience in product development and life cycle management for medical devices and combination products within the Pharmaceutical and/or Medical Device industry? Then we may have the perfect role for you. 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 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 • You should have a Master's degree in Medicine, Technology, Engineering, Pharmacy, Chemistry, or a related field.
• Experience with medical devices and combination products, as well as Design Control and regulatory requirements and standards, is an advantage
• Experience with digital medical device and combination products, as well as Design Control, regulatory requirements and standards, is an advantage 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 you are well-organised and have a flexible, but firm approach when making decisions. It is also 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
At Device Manufacturing Development (DMD QA), we are a team of 27 highly qualified professionals based at our Hillerød site. 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
At Novo Nordisk, we are a life-science company dedicated to improving the lives of patients around the world. We offer a dynamic and international work environment, with opportunities for professional and personal development. Contact
For further information, please contact Associate manager Carlos Gonçalves +45 3079 4194. Deadline
28th of May 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.
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 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 • You should have a Master's degree in Medicine, Technology, Engineering, Pharmacy, Chemistry, or a related field.
• Experience with medical devices and combination products, as well as Design Control and regulatory requirements and standards, is an advantage
• Experience with digital medical device and combination products, as well as Design Control, regulatory requirements and standards, is an advantage 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 you are well-organised and have a flexible, but firm approach when making decisions. It is also 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
At Device Manufacturing Development (DMD QA), we are a team of 27 highly qualified professionals based at our Hillerød site. 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
At Novo Nordisk, we are a life-science company dedicated to improving the lives of patients around the world. We offer a dynamic and international work environment, with opportunities for professional and personal development. Contact
For further information, please contact Associate manager Carlos Gonçalves +45 3079 4194. Deadline
28th of May 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.
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 1.5.2023, 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
Lignende jobs
-
Øvrige i Holte
Få mere info- Øvrige
- Holte
-
Øvrige i Hørsholm
Få mere info- Øvrige
- Hørsholm
-
Øvrige i Gentofte
Få mere info- Øvrige
- Gentofte
-
Øvrige i Gentofte
Få mere info- Øvrige
- Gentofte
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 |
|---|---|
| 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 |
| 26. oktober 2024 | 74 |
| 25. oktober 2024 | 69 |
| 24. oktober 2024 | 65 |
| 23. oktober 2024 | 58 |
| 22. oktober 2024 | 59 |
| 21. oktober 2024 | 56 |
| 20. oktober 2024 | 62 |
| 19. oktober 2024 | 62 |
| 18. oktober 2024 | 60 |
| 17. oktober 2024 | 65 |
| 16. oktober 2024 | 61 |
| 15. oktober 2024 | 66 |
| 14. oktober 2024 | 64 |
| 13. oktober 2024 | 69 |
| 12. oktober 2024 | 68 |
| 11. oktober 2024 | 68 |
| 10. oktober 2024 | 66 |
| 9. oktober 2024 | 62 |
| 8. oktober 2024 | 61 |