Senior QA Professional for establishing new GMP production facility
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Hillerød
In Novo Nordisk we drive our business to the benefit of patients. To be able to bring new innovative treatments to patients worldwide, we are expanding our capacities to support the company portfolio of future oral and injectable pharmaceuticals. Therefore, we are establishing a new, ground-breaking biotech API production facility in Hillerød.
In our quality organization supporting this capacity expansion, we are opening a position as senior quality professionals within the following GMP production disciplines: quality assurance of design, construction and qualification of facilities and equipment used for CIP/SIP and steam heat sterilization processes.
The new facility is for pharmaceutical production and must be designed in accordance with cGMP requirements (current Good Manufacturing Practice).
The position
You will be part of a highly skilled QA team allocated to perform quality assurance activities during design and construction of the new API production facility in Hillerød. The QA team will support the project throughout the project phases and after completion of the facility. Your primary task will be to secure the quality oversight and setting the direction for implementation of cGMP. As a QA professional you will be part of a QA team reporting to a senior manager.
Knowledge of facility/equipment qualification, knowledge of general cGMP requirements and the ability to perform quality oversight according to GMP are essential skills in the job. You should be able to communicate and explain the intent of the GMP requirements for the project team members and relevant project stakeholders.
Qualifications
To succeed in this role, you have:
• A Master’s degree within science or equivalent
• Experience from the pharmaceutical industry
• Knowledge of GMP validation (e.g. equipment/facility qualification, IT-validation, cleaning validation etc.)
• Knowledge of CIP/SIP/Autoclave processes
• Knowledge of GMP requirements for API production
• Communication skills
• Full English proficiency
On a personal level, you enjoy close teamwork, are a strong motivator of others and can stay balanced, when the waves get high. You thrive in a multicultural environment working across organizational borders and management levels. Building structures comes naturally to you and you enjoy simplifying wherever simplicity can benefit reaching the goals fast and in a sound and solid manner.
Join Novo Nordisk in times of expansion
Join us on our journey into the future and make your mark on a newly established organization that will be growing in the coming years.
Join us if you would like to work with dedicated and experienced QAs professionals, if you are curious about the opportunity to establish a factory that bridges new and automated technologies with strong know-how and expertise in biotech manufacturing; and if you are interested in starting up the new facility and when built become part of the team supporting production of the new products.
Contact
If you require further information, please contact Jakob Krog on phone +45 30750534
Deadline
13 Marts 2024
We will process applications as we receive them, so please do not hesitate to apply.
You do not need to attach a cover letter to your application, but please include a few sentences about your motivation to apply in your 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. 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.
In our quality organization supporting this capacity expansion, we are opening a position as senior quality professionals within the following GMP production disciplines: quality assurance of design, construction and qualification of facilities and equipment used for CIP/SIP and steam heat sterilization processes.
The new facility is for pharmaceutical production and must be designed in accordance with cGMP requirements (current Good Manufacturing Practice).
The position
You will be part of a highly skilled QA team allocated to perform quality assurance activities during design and construction of the new API production facility in Hillerød. The QA team will support the project throughout the project phases and after completion of the facility. Your primary task will be to secure the quality oversight and setting the direction for implementation of cGMP. As a QA professional you will be part of a QA team reporting to a senior manager.
Knowledge of facility/equipment qualification, knowledge of general cGMP requirements and the ability to perform quality oversight according to GMP are essential skills in the job. You should be able to communicate and explain the intent of the GMP requirements for the project team members and relevant project stakeholders.
Qualifications
To succeed in this role, you have:
• A Master’s degree within science or equivalent
• Experience from the pharmaceutical industry
• Knowledge of GMP validation (e.g. equipment/facility qualification, IT-validation, cleaning validation etc.)
• Knowledge of CIP/SIP/Autoclave processes
• Knowledge of GMP requirements for API production
• Communication skills
• Full English proficiency
On a personal level, you enjoy close teamwork, are a strong motivator of others and can stay balanced, when the waves get high. You thrive in a multicultural environment working across organizational borders and management levels. Building structures comes naturally to you and you enjoy simplifying wherever simplicity can benefit reaching the goals fast and in a sound and solid manner.
Join Novo Nordisk in times of expansion
Join us on our journey into the future and make your mark on a newly established organization that will be growing in the coming years.
Join us if you would like to work with dedicated and experienced QAs professionals, if you are curious about the opportunity to establish a factory that bridges new and automated technologies with strong know-how and expertise in biotech manufacturing; and if you are interested in starting up the new facility and when built become part of the team supporting production of the new products.
Contact
If you require further information, please contact Jakob Krog on phone +45 30750534
Deadline
13 Marts 2024
We will process applications as we receive them, so please do not hesitate to apply.
You do not need to attach a cover letter to your application, but please include a few sentences about your motivation to apply in your 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. 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 27.2.2024, 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.
- 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 |
|---|---|
| 26. november 2024 | 57 |
| 25. november 2024 | 55 |
| 24. november 2024 | 67 |
| 23. november 2024 | 66 |
| 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 |