Øvrige i Hillerød
Denne stilling er desværre ikke længere ledig.
Se alle ledige stillinger
Hillerød
Quality Assurance Professional for medical device
Are you looking for an exciting job opportunity as quality responsible? Do you want to play a vital part in the delivery of Novo Nordisk’s high-quality products to our patients? are you an ambitious and proactive team player who sees collaboration as key to success? Then you might be the colleague we are missing in the quality assurance department of Device Manufacturing & Sourcing. DMS Internal Manufacturing QA.
Currently we have two open positions within our team. We work in lovely surroundings in Novo Nordisk Device Manufacturing and Sourcing's buildings in Hillerød about 30 km north of Copenhagen.
We are part of the Novo Nordisk Quality organisation where we enforce compliance on behalf of authorities, support the business and at the same time strive towards making daily work for ourselves and our stakeholders less complex.
About the job
You will be joining a talented team of experienced and engaged QA professionals within Device Manufacturing & Sourcing.
As our new colleague you will be involved in many different responsibilities, but the following are some relevant pointers as to what the position entails:
Qualifications
As the ideal candidate you have previous experience within quality assurance, have worked with assembly or moulding processes. You have Master's degree in a relevant field e.g., mechanics / pharmaceutical sciences / manufacturing or have a similar background. Knowledge of device manufacturing, cGMP, validation, Lean and programming is an advantage. You are fluent in English, both written and spoken.
As a person, you bring a positive mindset, you are good at establishing relations with other people, communicate constructively, and you have a systematic approach to problem-solving. You are proactive and have a great interest in developing yourself and the team you are a part of.
It is a prerequisite that you are curious and seek to understand the underlying complexities and gain energy by going on the shopfloor and interact with your stakeholders or through dialog within your team.
The department
The department consists of 15 highly qualified QA engineers.
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. The main purpose of DMS QA is to safeguard patient safety, product quality and compliance.
Contact
If you want to know more about the position, please contact Associate Manager Paw Winther Brandt-Kofoed by phone on +45 3448 0098.
Deadline
13th November. Interviews will be conducted on an ongoing basis.
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.
Print job Send to e-mail
Are you looking for an exciting job opportunity as quality responsible? Do you want to play a vital part in the delivery of Novo Nordisk’s high-quality products to our patients? are you an ambitious and proactive team player who sees collaboration as key to success? Then you might be the colleague we are missing in the quality assurance department of Device Manufacturing & Sourcing. DMS Internal Manufacturing QA.
Currently we have two open positions within our team. We work in lovely surroundings in Novo Nordisk Device Manufacturing and Sourcing's buildings in Hillerød about 30 km north of Copenhagen.
We are part of the Novo Nordisk Quality organisation where we enforce compliance on behalf of authorities, support the business and at the same time strive towards making daily work for ourselves and our stakeholders less complex.
About the job
You will be joining a talented team of experienced and engaged QA professionals within Device Manufacturing & Sourcing.
As our new colleague you will be involved in many different responsibilities, but the following are some relevant pointers as to what the position entails:
- Responsible QA for the moulding and pre-assembly processes including QA oversight in the production facility
- Responsible QA for release of components produced from our internal production
- Support to deviation handling as well as change requests for the area
- Bring expert support to validation activities
- Always having a focus on continuous improvements and simplification of our processes
Qualifications
As the ideal candidate you have previous experience within quality assurance, have worked with assembly or moulding processes. You have Master's degree in a relevant field e.g., mechanics / pharmaceutical sciences / manufacturing or have a similar background. Knowledge of device manufacturing, cGMP, validation, Lean and programming is an advantage. You are fluent in English, both written and spoken.
As a person, you bring a positive mindset, you are good at establishing relations with other people, communicate constructively, and you have a systematic approach to problem-solving. You are proactive and have a great interest in developing yourself and the team you are a part of.
It is a prerequisite that you are curious and seek to understand the underlying complexities and gain energy by going on the shopfloor and interact with your stakeholders or through dialog within your team.
The department
The department consists of 15 highly qualified QA engineers.
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. The main purpose of DMS QA is to safeguard patient safety, product quality and compliance.
Contact
If you want to know more about the position, please contact Associate Manager Paw Winther Brandt-Kofoed by phone on +45 3448 0098.
Deadline
13th November. Interviews will be conducted on an ongoing basis.
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.
Print job Send to e-mail
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 20.10.2022, 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
Lignende jobs
-
Øvrige i Virum
Få mere info- Øvrige
- Virum
-
Øvrige i Allerød
Få mere info- Øvrige
- Allerød
-
Øvrige i Kongens Lyngby
Få mere info- Øvrige
- Kongens Lyngby
-
Øvrige i Rungsted Kyst
Få mere info- Øvrige
- Rungsted Kyst
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 |
|---|---|
| 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 |