Medical Devices Manufacturing Director
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Hillerød
Can you envision yourself setting the strategic direction, ensuring global quality compliance within device regulation, and overseeing the successful delivery of projects on a worldwide scale? Do you want to play a vital part in the delivery of Novo Nordisk’s high-quality products to our patients?
Then you might just be the Director we are looking for, read on and apply today for a life-changing career! The position
As a Director for Device Manufacturing & Sourcing QA (DMS QA) you will assure quality of all deliveries from Device Manufacturing & Sourcing (DMS). The main purpose of DMS QA is to safeguard patient safety, product quality and compliance and you will ensure that the area lives up to this purpose.
You will oversee the on-going corrective and preventive portfolio and ensure timely progress QA approval and control of the validated state for all Novo Nordisk owned equipment placed at the Contract manufacturing partners. Main responsibilities for the role will be to: • set the direction and strategy for the Quality function
• lead and develop your team
• secure the successful delivery of the portfolio of projects
• ensure status assignment of all components and pre-assembled motor modules produced world-wide
• drive the interpretation and implementation of Quality mindset within own department and future expansions The job base will be in Denmark, and 10-15 days of travelling per year is expected as the supplier and customer base are located world-wide.
The position has high level of impact on external stakeholders as the position holder will be representing Novo Nordisk and setting the direction for future business opportunities. Qualifications
To succeed in this role, you:
• hold a Master of Science in pharmacy, engineering, chemistry or similar
• have a proven track record of leadership and people management skills
• have experience from medical devices production
• have been involved in continuous improvement projects
• are fully proficient in English
Previous Quality Assurance experience is an advantage.
On a personal level, you have a high quality mindset and you are a strong communicator who can communicate in a clear, precise and respectful manner even though the scene for communication is intercultural. You take initiative and have a flexible attitude; although independent, you thrive in teamworking.
About the Department
DMS QA is located in Hillerød, 30 km north of Copenhagen. The department consists of 44 dedicated Quality engineers, QA technicians and QA professionals and are still growing. The area currently contains two teams but will be organized in four by March 1st. You will have 6 direct reports, 2 senior managers, 2 associate managers, a cLEAN partner, and an assistant. The department is responsible for the quality assurance of the in-house production as well as the global supply chain of high-quality components and preassembled parts for all Novo Nordisk prefilled and durable devices. Our external suppliers are in Europe, China, USA and Brazil. You will find that you have rich opportunities to create great results and develop yourself, both on a professional and on a personal level, and you will be trusted to execute your great ideas. Our DMS QA organization is a vital part of Novo Nordisk’s delivery to our patients, and we always welcome talented people who value a collaborative environment and would like to grow with us. Being a part of Novo Nordisk’s Device Manufacturing and Sourcing QA organization (DMS QA) means working with a global focus at one of the world’s largest and most successful pharmaceutical companies. 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 more information, please contact CVP Glauco Sanches by email [email protected] or phone +45 3075 3014. Deadline
07 January 2024
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.
Then you might just be the Director we are looking for, read on and apply today for a life-changing career! The position
As a Director for Device Manufacturing & Sourcing QA (DMS QA) you will assure quality of all deliveries from Device Manufacturing & Sourcing (DMS). The main purpose of DMS QA is to safeguard patient safety, product quality and compliance and you will ensure that the area lives up to this purpose.
You will oversee the on-going corrective and preventive portfolio and ensure timely progress QA approval and control of the validated state for all Novo Nordisk owned equipment placed at the Contract manufacturing partners. Main responsibilities for the role will be to: • set the direction and strategy for the Quality function
• lead and develop your team
• secure the successful delivery of the portfolio of projects
• ensure status assignment of all components and pre-assembled motor modules produced world-wide
• drive the interpretation and implementation of Quality mindset within own department and future expansions The job base will be in Denmark, and 10-15 days of travelling per year is expected as the supplier and customer base are located world-wide.
The position has high level of impact on external stakeholders as the position holder will be representing Novo Nordisk and setting the direction for future business opportunities. Qualifications
To succeed in this role, you:
• hold a Master of Science in pharmacy, engineering, chemistry or similar
• have a proven track record of leadership and people management skills
• have experience from medical devices production
• have been involved in continuous improvement projects
• are fully proficient in English
Previous Quality Assurance experience is an advantage.
On a personal level, you have a high quality mindset and you are a strong communicator who can communicate in a clear, precise and respectful manner even though the scene for communication is intercultural. You take initiative and have a flexible attitude; although independent, you thrive in teamworking.
About the Department
DMS QA is located in Hillerød, 30 km north of Copenhagen. The department consists of 44 dedicated Quality engineers, QA technicians and QA professionals and are still growing. The area currently contains two teams but will be organized in four by March 1st. You will have 6 direct reports, 2 senior managers, 2 associate managers, a cLEAN partner, and an assistant. The department is responsible for the quality assurance of the in-house production as well as the global supply chain of high-quality components and preassembled parts for all Novo Nordisk prefilled and durable devices. Our external suppliers are in Europe, China, USA and Brazil. You will find that you have rich opportunities to create great results and develop yourself, both on a professional and on a personal level, and you will be trusted to execute your great ideas. Our DMS QA organization is a vital part of Novo Nordisk’s delivery to our patients, and we always welcome talented people who value a collaborative environment and would like to grow with us. Being a part of Novo Nordisk’s Device Manufacturing and Sourcing QA organization (DMS QA) means working with a global focus at one of the world’s largest and most successful pharmaceutical companies. 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 more information, please contact CVP Glauco Sanches by email [email protected] or phone +45 3075 3014. Deadline
07 January 2024
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 15.12.2023, 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
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Statistik over udbudte jobs som øvrige i Hillerød
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Statistik over udbudte øvrige i Hillerød over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 5. juli 2024 | 73 |
| 4. juli 2024 | 74 |
| 3. juli 2024 | 67 |
| 2. juli 2024 | 66 |
| 1. juli 2024 | 64 |
| 30. juni 2024 | 74 |
| 29. juni 2024 | 74 |
| 28. juni 2024 | 75 |
| 27. juni 2024 | 71 |
| 26. juni 2024 | 67 |
| 25. juni 2024 | 66 |
| 24. juni 2024 | 67 |
| 23. juni 2024 | 72 |
| 22. juni 2024 | 69 |
| 21. juni 2024 | 67 |
| 20. juni 2024 | 65 |
| 19. juni 2024 | 72 |
| 18. juni 2024 | 74 |
| 17. juni 2024 | 74 |
| 16. juni 2024 | 81 |
| 15. juni 2024 | 80 |
| 14. juni 2024 | 79 |
| 13. juni 2024 | 73 |
| 12. juni 2024 | 75 |
| 11. juni 2024 | 72 |
| 10. juni 2024 | 67 |
| 9. juni 2024 | 82 |
| 8. juni 2024 | 82 |
| 7. juni 2024 | 81 |
| 6. juni 2024 | 76 |
| 5. juni 2024 | 75 |