Øvrige i Hillerød
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Hillerød
We are looking for a process supporter who would like to be part of a highly skilled production unit dedicated to making a difference for people living with Haemophilia and other chronic diseases.
About the department
You will be part of a dynamic business area which produces Active Pharmaceutical Ingredients (API) for patients across the world.
The open position is in New Product Entry, Biotech and Rare Diseases (BRD) API and is located in Hillerød. The department is responsible for transferring new products from Development to the production facilities in Hillerød, which includes both phase 3 production as well as process validation. The department is part of a larger production area with other departments such as production, equipment, maintenance, calibration and IT/Automization.
The Job
You will be a part of the Product Transfer team responsible for New Product Entry which currently consists of ca. 8 highly dedicated and skilled colleagues. As a process supporter in New Product Entry your key responsibility is to ensure the implementation of new API processes in the existing production facility together with your colleagues from production.
The processes include mammalian cultivation, recovery and purification. The tasks include knowledge transfer from our colleagues in development and you will identify and drive the necessary changes of the process via close collaboration with other key functions (eg. equipment responsible, downstream support, automation etc.). You will be writing procedures, process documents, protocols and change requests. Up to the first campaigns you will also be responsible for ensuring correct training and knowledge transfer to operators and process supporters in current production and will play a crucial role in supporting the running production. We expect you to have a keen eye for detail, a nag for analysing process data from development and production, a good understanding of production processes as well as a strong GMP mindset and stakeholder management.
Your key responsibilities will be:
Qualifications
You have an education as bioengineer, biotechnologist, biochemist or similar and have a minimum of 2-3 years of experience with production and/or development of pharmaceutical products. Preferably you have experience in mammalian cell cultivation or fermentation and/or recovery and purification with changing products under GMP .
As a person, you have strong analytical skills and preferably with solid knowledge of cell cultivation processes and/or purification processes. You are structured and proactive in your work, good at working independently, make data based decisions which both are within our GMP frame as well as support our strategic goals. LEAN is a natural part of your skill set. You will have several stakeholders across the organization and therefore your written and spoken communication skills in both Danish and English must be excellent. To succeed you need to be able to be calm and make decisions in a busy work environment where the agenda changes frequently.
Contact
For further information please contact Christiane Wiendahl at +45 30 79 48 62.
Deadline
6 November 2022
Please note that interviews will be carried out on an ongoing basis, so you are encouraged to apply as soon as possible.
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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About the department
You will be part of a dynamic business area which produces Active Pharmaceutical Ingredients (API) for patients across the world.
The open position is in New Product Entry, Biotech and Rare Diseases (BRD) API and is located in Hillerød. The department is responsible for transferring new products from Development to the production facilities in Hillerød, which includes both phase 3 production as well as process validation. The department is part of a larger production area with other departments such as production, equipment, maintenance, calibration and IT/Automization.
The Job
You will be a part of the Product Transfer team responsible for New Product Entry which currently consists of ca. 8 highly dedicated and skilled colleagues. As a process supporter in New Product Entry your key responsibility is to ensure the implementation of new API processes in the existing production facility together with your colleagues from production.
The processes include mammalian cultivation, recovery and purification. The tasks include knowledge transfer from our colleagues in development and you will identify and drive the necessary changes of the process via close collaboration with other key functions (eg. equipment responsible, downstream support, automation etc.). You will be writing procedures, process documents, protocols and change requests. Up to the first campaigns you will also be responsible for ensuring correct training and knowledge transfer to operators and process supporters in current production and will play a crucial role in supporting the running production. We expect you to have a keen eye for detail, a nag for analysing process data from development and production, a good understanding of production processes as well as a strong GMP mindset and stakeholder management.
Your key responsibilities will be:
- Coordination of activities with internal and external stakeholders (process development, equipment, facility, production, automization and QA)
- Responsible for preparing and supporting campaigns for new products, including required documentation in accordance with the current standards and legislations, change requests and process deviations
- Ensure technology, process and knowledge transfer between development and production
- Troubleshooting related to the daily manufacturing of new products
- Initiate problem solving (A3 or similar) for observed process deviations or other issues in the production of the new products
Qualifications
You have an education as bioengineer, biotechnologist, biochemist or similar and have a minimum of 2-3 years of experience with production and/or development of pharmaceutical products. Preferably you have experience in mammalian cell cultivation or fermentation and/or recovery and purification with changing products under GMP .
As a person, you have strong analytical skills and preferably with solid knowledge of cell cultivation processes and/or purification processes. You are structured and proactive in your work, good at working independently, make data based decisions which both are within our GMP frame as well as support our strategic goals. LEAN is a natural part of your skill set. You will have several stakeholders across the organization and therefore your written and spoken communication skills in both Danish and English must be excellent. To succeed you need to be able to be calm and make decisions in a busy work environment where the agenda changes frequently.
Contact
For further information please contact Christiane Wiendahl at +45 30 79 48 62.
Deadline
6 November 2022
Please note that interviews will be carried out on an ongoing basis, so you are encouraged to apply as soon as possible.
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 14.10.2022, 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
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.
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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 |