Senior QA Professional for Medical Devices
Denne stilling er desværre ikke længere ledig.
Se alle ledige stillinger
Hillerød
Are you looking for an exciting opportunity to advance your career in Quality Assurance? Are you passionate about ensuring regulatory compliance and advising your team on compliant solutions for medical devices? With your experience in product development and life cycle management, you'll work alongside a team of passionate professionals to launch important medical devices to patients. Don't miss out on this chance to take your career to the next level – apply now!
The position
As our Senior 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 and give impact on a broad range of the crucial processes to deliver products to our patients. The focus of this role will be to 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 ’s device products portfolio. Main responsibilities will also include: • finding solutions through a solid process and business understanding
• giving proactive advice to our stakeholders to secure we establish simple compliant solutions within processes such as: Design Control, Risk Management, and testing.
• playing an important role in ensuring that we build competent skills in Quality Assurance and have an in-depth understanding of relevant regulatory requirements This position will enable you 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 To succeed in this role, you:
• hold a Master's degree in Technology, Engineering, Pharmacy, Chemistry, or a related field
• have extensive experience from the pharmaceutical industry either from production, QA, or QC where you have gained a solid and up-to-date knowledge of quality and GMP requirements
• are fluent in English, both written and spoken
Experience with Medical Devices Design Control, regulations and standards will be seen as an advantage, as well as experience with connected medical devices, combination products and needle-based automated injection systems.
Ready to lead and build strong relationships? Bring your excellent cooperation skills and flexible decision-making approach to our team. With an open-minded and positive attitude, you're eager to make a difference and learn. If this sounds like you, but you don't meet all the criteria, contact our hiring manager to see if you're eligible!
About the department
At Device Manufacturing Development (DMD QA), we are a department of 42 highly qualified professionals based at our Hillerød site, with diverse backgrounds and interests.
In team Product development QA we are 14 highly skilled professionals waiting for you to join us. We are responsible for ensuring the quality and compliance of all processes in 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
At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact
For further information, please contact QA manager Jane Frederiksen +. Deadline
17 March 2024
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 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.
The position
As our Senior 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 and give impact on a broad range of the crucial processes to deliver products to our patients. The focus of this role will be to 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 ’s device products portfolio. Main responsibilities will also include: • finding solutions through a solid process and business understanding
• giving proactive advice to our stakeholders to secure we establish simple compliant solutions within processes such as: Design Control, Risk Management, and testing.
• playing an important role in ensuring that we build competent skills in Quality Assurance and have an in-depth understanding of relevant regulatory requirements This position will enable you 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 To succeed in this role, you:
• hold a Master's degree in Technology, Engineering, Pharmacy, Chemistry, or a related field
• have extensive experience from the pharmaceutical industry either from production, QA, or QC where you have gained a solid and up-to-date knowledge of quality and GMP requirements
• are fluent in English, both written and spoken
Experience with Medical Devices Design Control, regulations and standards will be seen as an advantage, as well as experience with connected medical devices, combination products and needle-based automated injection systems.
Ready to lead and build strong relationships? Bring your excellent cooperation skills and flexible decision-making approach to our team. With an open-minded and positive attitude, you're eager to make a difference and learn. If this sounds like you, but you don't meet all the criteria, contact our hiring manager to see if you're eligible!
About the department
At Device Manufacturing Development (DMD QA), we are a department of 42 highly qualified professionals based at our Hillerød site, with diverse backgrounds and interests.
In team Product development QA we are 14 highly skilled professionals waiting for you to join us. We are responsible for ensuring the quality and compliance of all processes in 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
At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact
For further information, please contact QA manager Jane Frederiksen +. Deadline
17 March 2024
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 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 28.2.2024, 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.
- 09.04.2024
- Øvrige
- Hillerød
Lignende jobs
-
Øvrige i Vedbæk
Få mere info- Øvrige
- Vedbæk
-
Øvrige i Rungsted Kyst
Få mere info- Øvrige
- Rungsted Kyst
-
Øvrige i Nivå
Få mere info- Øvrige
- Nivå
-
Øvrige i Værløse
Få mere info- Øvrige
- Værløse
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 over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 29. april 2024 | 70 |
| 28. april 2024 | 81 |
| 27. april 2024 | 82 |
| 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 |
| 18. april 2024 | 78 |
| 17. april 2024 | 76 |
| 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 |