Senior Validation Professional
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Hillerød
Are you looking for a new role with responsibility for quality assurance of several APIs (Active Pharmaceuticals Ingredients) produced in Hillerød? Do you want to have influence and set directions in setting the right level of compliance, optimizing our processes and establish new processes in collaboration with stakeholders? Do you want to be part of a fantastic team that values team spirit, empowerment, and good collaboration with our stakeholders? Then it is the right time to join us, read more and apply!
The Position
In QA we have the quality oversight and are physically present in the production to observe performed processes and help solve issues in real time. For this role you will join a team of 11 competent colleagues that hold 13 different educational backgrounds and therefore help each other develop and grow on a daily basis.
Among daily duties, you will:
• Review and approve of validation documentation according to Science and Risk-based Validation
• Perform review of batch and process related documentation from our stakeholders including deviations, change requests, Standard Operating Procedures etc.
• Set directions and deliver results which have a significant impact within the context of our business
• Assure that the documentation related to the manufacture of drug product for the market is compliant with internal and external requirements
• Getting products out to our patients at the right quality and in a timely manner
You will be a validation QA professional, and perhaps a Quality Person Delegate, and you will have the overview of the processes within production of API in Hillerød.
Qualifications
We are looking for a candidate that has a risk-based approach to the manufacturing process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct.
To succeed in this role, you:
• Hold Master’s degree as cand. pharm, cand. Scient, veterinary medicine or similar
• Have at least 1 year experience with validation
• Have at least 1 year relevant experience within QA or production support
• Have at least 1 year relevant experience with GMP (Good Manufacturing Practice)
• Have full proficiency in both Danish and English
On a personal note, you have strong communication skills and are eager to set direction and to ensure compliance, in close collaboration with colleagues and stakeholders. You are a self-driven and independent person with a high sense of responsibility and initiative who can prioritise your many different tasks.
Moreover, you thrive in a dynamic environment, where teamwork is on the top of the agenda, and like working with many different stakeholders.
About the department
Biotech Rare Disease Quality Assurance Active Pharmaceuticals Ingredients Denmark is a fantastic department to be in with approximately 50 skilled and motivated colleagues based in both Gentofte, Hillerød and Kalundborg.
We work with the possibility to have a great individual responsibility but are always there to help each other ensuring engagement and a lot of good relations every day. We are proud to work in a fast-growing and ambitious part of Novo Nordisk.
We can offer a great working environment with high level of team spirit as well as highly skilled, ambitious, and engaged colleagues. We work very well together while we have fun.
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 further information, please contact Associate Manager Jane Frederiksen +45 3079 9796
Deadline
15 January 2023
Please note that interviews will be held on a continuous basis, so we encourage you to apply as soon as possible.
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.
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The Position
In QA we have the quality oversight and are physically present in the production to observe performed processes and help solve issues in real time. For this role you will join a team of 11 competent colleagues that hold 13 different educational backgrounds and therefore help each other develop and grow on a daily basis.
Among daily duties, you will:
• Review and approve of validation documentation according to Science and Risk-based Validation
• Perform review of batch and process related documentation from our stakeholders including deviations, change requests, Standard Operating Procedures etc.
• Set directions and deliver results which have a significant impact within the context of our business
• Assure that the documentation related to the manufacture of drug product for the market is compliant with internal and external requirements
• Getting products out to our patients at the right quality and in a timely manner
You will be a validation QA professional, and perhaps a Quality Person Delegate, and you will have the overview of the processes within production of API in Hillerød.
Qualifications
We are looking for a candidate that has a risk-based approach to the manufacturing process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct.
To succeed in this role, you:
• Hold Master’s degree as cand. pharm, cand. Scient, veterinary medicine or similar
• Have at least 1 year experience with validation
• Have at least 1 year relevant experience within QA or production support
• Have at least 1 year relevant experience with GMP (Good Manufacturing Practice)
• Have full proficiency in both Danish and English
On a personal note, you have strong communication skills and are eager to set direction and to ensure compliance, in close collaboration with colleagues and stakeholders. You are a self-driven and independent person with a high sense of responsibility and initiative who can prioritise your many different tasks.
Moreover, you thrive in a dynamic environment, where teamwork is on the top of the agenda, and like working with many different stakeholders.
About the department
Biotech Rare Disease Quality Assurance Active Pharmaceuticals Ingredients Denmark is a fantastic department to be in with approximately 50 skilled and motivated colleagues based in both Gentofte, Hillerød and Kalundborg.
We work with the possibility to have a great individual responsibility but are always there to help each other ensuring engagement and a lot of good relations every day. We are proud to work in a fast-growing and ambitious part of Novo Nordisk.
We can offer a great working environment with high level of team spirit as well as highly skilled, ambitious, and engaged colleagues. We work very well together while we have fun.
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 further information, please contact Associate Manager Jane Frederiksen +45 3079 9796
Deadline
15 January 2023
Please note that interviews will be held on a continuous basis, so we encourage you to apply as soon as possible.
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 12.10.2022, 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
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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. oktober 2024 | 58 |
| 4. oktober 2024 | 54 |
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| 2. oktober 2024 | 55 |
| 1. oktober 2024 | 51 |
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| 28. september 2024 | 75 |
| 27. september 2024 | 75 |
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| 23. september 2024 | 81 |
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| 21. september 2024 | 83 |
| 20. september 2024 | 81 |
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| 18. september 2024 | 82 |
| 17. september 2024 | 82 |
| 16. september 2024 | 80 |
| 15. september 2024 | 85 |
| 14. september 2024 | 87 |
| 13. september 2024 | 80 |
| 12. september 2024 | 68 |
| 11. september 2024 | 65 |
| 10. september 2024 | 66 |
| 9. september 2024 | 69 |
| 8. september 2024 | 69 |
| 7. september 2024 | 70 |
| 6. september 2024 | 70 |
| 5. september 2024 | 70 |