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Hillerød
We are looking for a skilled project manager 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 deseases.
About the production department
You will be part of a dynamic business area which produces Active Pharmaceutical Ingredients (API) for patients across the world.
You will be part of a dynamic business area which produce Active Pharmaceutical Ingredients (API) for patients across the world.
BRD API DK production site 25K consists of 3 departments covering 11 teams. We are situated in Hillerød and produce products for chronic diseases as for example haemophilia disorders. As we implement several new products in the upcoming years, we are responsible for both market production, phase 3 GMP productions as well as process validation.
The open position is in New Product Entry, which is linked to the production department. The department is responsible for transferring new product from Development to the production facilities and secure the production of the new products.
The Job
As a project manager in the team, you will be responsible for coordinating activities around entry of new products in our production facilities and bridge between development and production. This includes stakeholder management and communication with eg. Development, QC, QA, production, equipment responsible, raw material responsible and process supporter. Apart from that you will play a crucial role in the cross organisational project set up and will chair the Technology Transfer Team which ensures the implementation of new products and processes in production. You will present project progress in steering groups and project core teams. You will also participate in coordination between the new products as the planning of different products always interact due to production- and manning resources.
Your key responsibilities will be:
Qualifications
You have an education as bioengineer, biotechnologist, biochemist or similar and have a minimum of 6-8 years of experience with production and/or development of pharmaceutical products. In addition to that you have solid experience with coordination and planning of projects.
As a person, you are highly structured with very good planning and coordination skills. You are able to have overview over many parallel activities and are able to see bottle necks and identify task which are on a critical path. You are proactive in your work and will never compromise on quality. GMP and 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 as well as your presentation skills in both Danish and English must be excellent. You have a strong mind set of team work as well as the will to succeed with your project. You need to be able to keep a cool head 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
13.11.22
We will conduct interviews on an ongoing basis so earlier applications are encouraged.
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 production department
You will be part of a dynamic business area which produces Active Pharmaceutical Ingredients (API) for patients across the world.
You will be part of a dynamic business area which produce Active Pharmaceutical Ingredients (API) for patients across the world.
BRD API DK production site 25K consists of 3 departments covering 11 teams. We are situated in Hillerød and produce products for chronic diseases as for example haemophilia disorders. As we implement several new products in the upcoming years, we are responsible for both market production, phase 3 GMP productions as well as process validation.
The open position is in New Product Entry, which is linked to the production department. The department is responsible for transferring new product from Development to the production facilities and secure the production of the new products.
The Job
As a project manager in the team, you will be responsible for coordinating activities around entry of new products in our production facilities and bridge between development and production. This includes stakeholder management and communication with eg. Development, QC, QA, production, equipment responsible, raw material responsible and process supporter. Apart from that you will play a crucial role in the cross organisational project set up and will chair the Technology Transfer Team which ensures the implementation of new products and processes in production. You will present project progress in steering groups and project core teams. You will also participate in coordination between the new products as the planning of different products always interact due to production- and manning resources.
Your key responsibilities will be:
- Coordination of activities with internal and external stakeholders (e.g. process development, equipment, facility, production, QC and QA)
- Establishment of a clear and detailed activity plan
- Coordination of activities around phase 3 production
- Coordination of activities for process characterization and validation
Qualifications
You have an education as bioengineer, biotechnologist, biochemist or similar and have a minimum of 6-8 years of experience with production and/or development of pharmaceutical products. In addition to that you have solid experience with coordination and planning of projects.
As a person, you are highly structured with very good planning and coordination skills. You are able to have overview over many parallel activities and are able to see bottle necks and identify task which are on a critical path. You are proactive in your work and will never compromise on quality. GMP and 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 as well as your presentation skills in both Danish and English must be excellent. You have a strong mind set of team work as well as the will to succeed with your project. You need to be able to keep a cool head 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
13.11.22
We will conduct interviews on an ongoing basis so earlier applications are encouraged.
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 28.10.2022, 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 øvrige i Hillerød over tid
Dato | Alle jobs som øvrige |
---|---|
6. september 2024 | 70 |
5. september 2024 | 70 |
4. september 2024 | 64 |
3. september 2024 | 63 |
2. september 2024 | 60 |
1. september 2024 | 63 |
31. august 2024 | 70 |
30. august 2024 | 71 |
29. august 2024 | 68 |
28. august 2024 | 70 |
27. august 2024 | 70 |
26. august 2024 | 67 |
25. august 2024 | 75 |
24. august 2024 | 74 |
23. august 2024 | 79 |
22. august 2024 | 75 |
21. august 2024 | 72 |
20. august 2024 | 70 |
19. august 2024 | 61 |
18. august 2024 | 69 |
17. august 2024 | 68 |
16. august 2024 | 67 |
15. august 2024 | 66 |
14. august 2024 | 74 |
13. august 2024 | 71 |
12. august 2024 | 71 |
11. august 2024 | 75 |
10. august 2024 | 75 |
9. august 2024 | 72 |
8. august 2024 | 68 |
7. august 2024 | 60 |
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