Quality Engineer for Medical Device Suppliers
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Hillerød
Are you searching for a dynamic international opportunity as a Quality Responsible for Suppliers Worldwide? Are you skilled in collaborating, coaching, and challenging external suppliers on a daily basis while being a part of a global expansion of suppliers?
If you desire a role in a department with exceptional colleagues and ambitions world-class-goals, flexibility and work life balance then we may have just the right job for you in the Quality Assurance Department of Device Manufacturing & Sourcing (DMS) External Manufacturing QA. In DMS External Manufacturing QA, we seek a motivated and dedicated engineer who will be responsible for the quality assurance of specific components for Novo Nordisk medical devices. Our suppliers are located in Scandinavia, Europe, China, USA, and Brazil. As a part of the Novo Nordisk Quality organisation, we enforce compliance on behalf of authorities, support the business and, simultaneously strive to make daily work for ourselves and our stakeholders more manageable, all while being flexible in the job.
The position
You will independently, with the support of your colleagues and via close dialogue with process experts, supply managers, Device Manufacturing Development and R&D, have the responsibility for the quality output of our suppliers. Your main responsibility is to oversee the quality level of products our suppliers provide. This includes creating and maintaining quality contracts, handling of deviations, change control, and facilitating continuous improvement without compromising patient safety. Our suppliers are working within the fields of injection moulding, advanced assembly processes, electronic production and metal processing. Around 10-20 travel days a year can be expected, building relations and expanding your knowledge in a complex and challenging business environment. Quality mindset, simplicity and Winning culture are integrated concepts in our work. 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. We offer an internationally exciting job with lots of challenges. We implement individual development plans which support your growth and assist you in achieving your professional ambitions. We ensure that there is a good work-life balance. We share an informal tone, and we enjoy learning from each other, striving to deepen our understanding of an increasingly complex area. Qualifications
As the ideal candidate you have previous experience within quality assurance, have worked with suppliers in a global environment and with advanced assembly or moulding processes. You have a Master´s degree within the fields of mechanics/electronics/manufacturing or have a similar engineering degree. Knowledge of ISO13485, cGMP, validation, Lean and programming is an advantage. You are fluent in English, both written and spoken. On a personal level, you are ambitious and have a great interest in developing yourself. You make a difference and through your commitment and perseverance, you complete your tasks in close cooperation with your colleagues. You are collaborative and enjoy sharing knowledge and experiences with stakeholders. You're independent and not afraid to take the initiative. We also welcome applicants from other branches, as long as you share our passion for quality, GMP and problem-solving and are keen to acquire professional competencies to become what we describe as an “ideal candidate”.
Also, if you are in the fall of your professional career and would enjoy requiring new competencies you are most welcomed to apply.
Let’s talk, even if you are looking for a position with reduced hours. About the department
The department consists of 15 highly qualified QA engineers who have responsibility for the quality of electronics, springs and plastic components produced by Novo Nordisk suppliers. We work in lovely surroundings in Novo Nordisk Device Manufacturing and Sourcing's buildings in Hillerød about 30 km north of Copenhagen. Working at Novo Nordisk
To work for Novo Nordisk, you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development. Contact
If you want to know more about the position, please contact Senior Manager Gert Petersen by phone on +45 30 75 75 97. Deadline
Deadline to apply for this position is February 6th 2023.
Applications will be considered on an ongoing basis. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 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.
If you desire a role in a department with exceptional colleagues and ambitions world-class-goals, flexibility and work life balance then we may have just the right job for you in the Quality Assurance Department of Device Manufacturing & Sourcing (DMS) External Manufacturing QA. In DMS External Manufacturing QA, we seek a motivated and dedicated engineer who will be responsible for the quality assurance of specific components for Novo Nordisk medical devices. Our suppliers are located in Scandinavia, Europe, China, USA, and Brazil. As a part of the Novo Nordisk Quality organisation, we enforce compliance on behalf of authorities, support the business and, simultaneously strive to make daily work for ourselves and our stakeholders more manageable, all while being flexible in the job.
The position
You will independently, with the support of your colleagues and via close dialogue with process experts, supply managers, Device Manufacturing Development and R&D, have the responsibility for the quality output of our suppliers. Your main responsibility is to oversee the quality level of products our suppliers provide. This includes creating and maintaining quality contracts, handling of deviations, change control, and facilitating continuous improvement without compromising patient safety. Our suppliers are working within the fields of injection moulding, advanced assembly processes, electronic production and metal processing. Around 10-20 travel days a year can be expected, building relations and expanding your knowledge in a complex and challenging business environment. Quality mindset, simplicity and Winning culture are integrated concepts in our work. 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. We offer an internationally exciting job with lots of challenges. We implement individual development plans which support your growth and assist you in achieving your professional ambitions. We ensure that there is a good work-life balance. We share an informal tone, and we enjoy learning from each other, striving to deepen our understanding of an increasingly complex area. Qualifications
As the ideal candidate you have previous experience within quality assurance, have worked with suppliers in a global environment and with advanced assembly or moulding processes.
Also, if you are in the fall of your professional career and would enjoy requiring new competencies you are most welcomed to apply.
Let’s talk, even if you are looking for a position with reduced hours. About the department
The department consists of 15 highly qualified QA engineers who have responsibility for the quality of electronics, springs and plastic components produced by Novo Nordisk suppliers. We work in lovely surroundings in Novo Nordisk Device Manufacturing and Sourcing's buildings in Hillerød about 30 km north of Copenhagen. Working at Novo Nordisk
To work for Novo Nordisk, you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development. Contact
If you want to know more about the position, please contact Senior Manager Gert Petersen by phone on +45 30 75 75 97. Deadline
Deadline to apply for this position is February 6th 2023.
Applications will be considered on an ongoing basis. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 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 5.1.2023, 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.
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Statistik over udbudte øvrige over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 26. april 2024 | 78 |
| 25. april 2024 | 73 |
| 24. april 2024 | 71 |
| 23. april 2024 | 69 |
| 22. april 2024 | 84 |
| 21. april 2024 | 83 |
| 20. april 2024 | 84 |
| 19. april 2024 | 82 |
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| 16. april 2024 | 70 |
| 15. april 2024 | 81 |
| 14. april 2024 | 86 |
| 13. april 2024 | 84 |
| 12. april 2024 | 82 |
| 11. april 2024 | 80 |
| 10. april 2024 | 73 |
| 9. april 2024 | 68 |
| 8. april 2024 | 70 |
| 7. april 2024 | 80 |
| 6. april 2024 | 80 |
| 5. april 2024 | 77 |
| 4. april 2024 | 75 |
| 3. april 2024 | 76 |
| 2. april 2024 | 77 |
| 1. april 2024 | 84 |
| 31. marts 2024 | 87 |
| 30. marts 2024 | 87 |
| 29. marts 2024 | 91 |
| 28. marts 2024 | 86 |
| 27. marts 2024 | 86 |