Senior QA Professional for Aseptic Production
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Hillerød
Are you passionate about ensuring the highest quality products for patients? Are you ready to take on a key role in QA, acting as a Subject Matter Expert in aseptic manufacturing? Join us as a Senior QA Professional, where you'll be a role model for collaboration, setting compliance standards, and applying GMP regulations to make a real impact, apply now!
The Position
As QA, our key task is to ensure products of the highest quality to serve our patients and our main responsibility is to set direction for quality and compliance. QA oversight is a huge part of our job both during the aseptic production, review of several types of documents and release of products.
Your tasks will include:
• Acting as a QA Subject Matter Expert within aseptic manufacturing both internally in QA and as sparring for our stakeholders
• Being present at shopfloor to ensure good collaboration with stakeholders, to support improvement projects and to handle/support deviations at point of cause
• Ensuring validation of production processes
• Acting as partners for production and our support units when there are questions about quality or compliance
• Be a Qualified Person delegate (QPd)
As a Senior QA Professional, you are expected to be a role model for good collaboration, setting direction for the right level of compliance and to be able to apply the GMP regulations in practice. Qualifications
To succeed in this role, you:
• Hold a Masters’ degree in Pharmacy, or other related subjects
• Have extensive experience in aseptic production, preferably in a QA role
• Preferably have validation experience
• Are fluent in both English and Danish
Since you will be a QPd, we will have to verify you have The Danish Medicines Agency's qualification and experience requirements for a QP are based on article 49 of Directive 2001/83/EC and article 53 of Directive 2001/82/EC – we kindly ask you to verify if you align to these requirements before applying.
As a person, you are detail-oriented and thorough, curious by nature and have strong communication skills. You enjoy working in a dynamic environment where you can take responsibility but are also a great team-player who finds it essential to succeed as a group. About the department
At Injectable Finished Products (IFP) QA Hillerød we are responsible for quality assurance of the aseptic production in Hillerød. It is our responsibility to ensure that the documentation meets the regulatory GMP requirements.
We are a well-functioning team of 70 dedicated and engaged employees divided in 6 teams. We work together as a team with a desire to solve challenges through open and honest dialogue. We always work on improving our way of working and we appreciate new ideas and continues improvements.
Working at Novo Nordisk
At Novo Nordisk, 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
If you have any questions about the position, you are welcome to contact Associate Manager Elika Khaghani at +45 34482861
Deadline
11 February 2024
Please note that interviews will be held ongoing, so we encourage you to apply sooner rather than later.
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.
The Position
As QA, our key task is to ensure products of the highest quality to serve our patients and our main responsibility is to set direction for quality and compliance. QA oversight is a huge part of our job both during the aseptic production, review of several types of documents and release of products.
Your tasks will include:
• Acting as a QA Subject Matter Expert within aseptic manufacturing both internally in QA and as sparring for our stakeholders
• Being present at shopfloor to ensure good collaboration with stakeholders, to support improvement projects and to handle/support deviations at point of cause
• Ensuring validation of production processes
• Acting as partners for production and our support units when there are questions about quality or compliance
• Be a Qualified Person delegate (QPd)
As a Senior QA Professional, you are expected to be a role model for good collaboration, setting direction for the right level of compliance and to be able to apply the GMP regulations in practice. Qualifications
To succeed in this role, you:
• Hold a Masters’ degree in Pharmacy, or other related subjects
• Have extensive experience in aseptic production, preferably in a QA role
• Preferably have validation experience
• Are fluent in both English and Danish
Since you will be a QPd, we will have to verify you have The Danish Medicines Agency's qualification and experience requirements for a QP are based on article 49 of Directive 2001/83/EC and article 53 of Directive 2001/82/EC – we kindly ask you to verify if you align to these requirements before applying.
As a person, you are detail-oriented and thorough, curious by nature and have strong communication skills. You enjoy working in a dynamic environment where you can take responsibility but are also a great team-player who finds it essential to succeed as a group. About the department
At Injectable Finished Products (IFP) QA Hillerød we are responsible for quality assurance of the aseptic production in Hillerød. It is our responsibility to ensure that the documentation meets the regulatory GMP requirements.
We are a well-functioning team of 70 dedicated and engaged employees divided in 6 teams. We work together as a team with a desire to solve challenges through open and honest dialogue. We always work on improving our way of working and we appreciate new ideas and continues improvements.
Working at Novo Nordisk
At Novo Nordisk, 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
If you have any questions about the position, you are welcome to contact Associate Manager Elika Khaghani at +45 34482861
Deadline
11 February 2024
Please note that interviews will be held ongoing, so we encourage you to apply sooner rather than later.
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 18.12.2023, 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 |
|---|---|
| 22. november 2024 | 65 |
| 21. november 2024 | 64 |
| 20. november 2024 | 63 |
| 19. november 2024 | 64 |
| 18. november 2024 | 62 |
| 17. november 2024 | 71 |
| 16. november 2024 | 71 |
| 15. november 2024 | 69 |
| 14. november 2024 | 68 |
| 13. november 2024 | 59 |
| 12. november 2024 | 63 |
| 11. november 2024 | 61 |
| 10. november 2024 | 63 |
| 9. november 2024 | 63 |
| 8. november 2024 | 63 |
| 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 |