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Do you have experience with formulation of drug products, and would you like to support global manufacturing of Novo Nordisk’s Injectable Finished Products (IFP)? If so, we have a job opening for you.
About the Department
Our department, Site Support and Improvements, is part of Manufacturing Development (ManDev), which is a part of the IFP organisation. In ManDev, we have expert knowledge about our products and the processes needed to support our production sites, world-wide.
As a member of our team, you will be working together with 10 formulation/filtration experts located in Bagsværd, Denmark. We are centrally positioned in the organisation and take ownership & share responsibility for the product quality of each drug product manufactured in IFP. The team has a diverse profile both in age, gender and nationality which has proven a great strength both socially and professionally.
The Position
The ideal candidate has several years of experience within drug product formulation and GMP production. However, we are also looking for team members with the right mindset and a let’s-make-it-work attitude. So, if your credentials are not a 1:1 match but you’re willing to learn you should not hesitate to apply.
The position is at a crossroad where many areas of responsibility meet, and it is therefore important that you are good at prioritizing tasks and feel good in situations where roles and responsibilities are not always sharply defined. You will be responsible for supplying a broad range of stakeholders in NN, with detailed knowledge of the products and processes. Here it is key that you have a sound nature of critical thinking in order to most efficiently support these stakeholders in each case.
The area of work in the position includes:
You are by nature curious, pro-active and coping well in an environment where priorities can change and where some deadlines are short. You excel in these behaviours in order to best serve the production sites and to support you colleagues. You are expected to have strong organisation skills and display a reliable overview of your own deadlines, in order to deliver to them.
Qualifications
You hold a Bachelor's Degree or higher academic education background within chemistry, engineering, pharmacy or similar.
Preferrable, but not necessary, you have 3+ years’ experience working within a GMP environment, preferably in drug product manufacturing.
It is advantageous, if you additionally to formulation knowledge, have experience with sterile filtration, product validation and/or regulatory affairs.
Excellent communication skills with experience of working effectively with stakeholders.
You are fluent in spoken and written English.
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
For further information you are welcome to contact Søren Alvarez Utoft (Associate Manager) on: +45-30799981 [email protected]
Deadline
November 15th 2022. We may conduct interviews before the deadline. Therefore, we may take the liberty to close for new applicants before the deadline
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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About the Department
Our department, Site Support and Improvements, is part of Manufacturing Development (ManDev), which is a part of the IFP organisation. In ManDev, we have expert knowledge about our products and the processes needed to support our production sites, world-wide.
As a member of our team, you will be working together with 10 formulation/filtration experts located in Bagsværd, Denmark. We are centrally positioned in the organisation and take ownership & share responsibility for the product quality of each drug product manufactured in IFP. The team has a diverse profile both in age, gender and nationality which has proven a great strength both socially and professionally.
The Position
The ideal candidate has several years of experience within drug product formulation and GMP production. However, we are also looking for team members with the right mindset and a let’s-make-it-work attitude. So, if your credentials are not a 1:1 match but you’re willing to learn you should not hesitate to apply.
The position is at a crossroad where many areas of responsibility meet, and it is therefore important that you are good at prioritizing tasks and feel good in situations where roles and responsibilities are not always sharply defined. You will be responsible for supplying a broad range of stakeholders in NN, with detailed knowledge of the products and processes. Here it is key that you have a sound nature of critical thinking in order to most efficiently support these stakeholders in each case.
The area of work in the position includes:
- Giving input to critical production deviations from IFP sites, where product quality is concerned.
- Providing product information to regulatory affairs.
- Supporting sites during routine inspections from health authorities.
- Maintaining and updating secure product specific documents.
- Participate in upscaling or transferring of novel products to production sites.
- Review of validation and registration documents.
- Assist and drive optimisation projects to improve IFP formulation activities.
You are by nature curious, pro-active and coping well in an environment where priorities can change and where some deadlines are short. You excel in these behaviours in order to best serve the production sites and to support you colleagues. You are expected to have strong organisation skills and display a reliable overview of your own deadlines, in order to deliver to them.
Qualifications
You hold a Bachelor's Degree or higher academic education background within chemistry, engineering, pharmacy or similar.
Preferrable, but not necessary, you have 3+ years’ experience working within a GMP environment, preferably in drug product manufacturing.
It is advantageous, if you additionally to formulation knowledge, have experience with sterile filtration, product validation and/or regulatory affairs.
Excellent communication skills with experience of working effectively with stakeholders.
You are fluent in spoken and written English.
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
For further information you are welcome to contact Søren Alvarez Utoft (Associate Manager) on: +45-30799981 [email protected]
Deadline
November 15th 2022. We may conduct interviews before the deadline. Therefore, we may take the liberty to close for new applicants before the deadline
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 Bagsværd.
Jobbet er oprettet på vores service den 28.4.2022, 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
- Bagsværd
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Statistik over udbudte jobs som øvrige i Bagsværd
Herunder ser du udviklingen i udbudte øvrige i Bagsværd 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 Bagsværd over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 23. november 2024 | 76 |
| 22. november 2024 | 70 |
| 21. november 2024 | 65 |
| 20. november 2024 | 66 |
| 19. november 2024 | 65 |
| 18. november 2024 | 64 |
| 17. november 2024 | 73 |
| 16. november 2024 | 73 |
| 15. november 2024 | 70 |
| 14. november 2024 | 69 |
| 13. november 2024 | 66 |
| 12. november 2024 | 62 |
| 11. november 2024 | 60 |
| 10. november 2024 | 62 |
| 9. november 2024 | 62 |
| 8. november 2024 | 59 |
| 7. november 2024 | 58 |
| 6. november 2024 | 57 |
| 5. november 2024 | 57 |
| 4. november 2024 | 53 |
| 3. november 2024 | 58 |
| 2. november 2024 | 57 |
| 1. november 2024 | 56 |
| 31. oktober 2024 | 64 |
| 30. oktober 2024 | 50 |
| 29. oktober 2024 | 49 |
| 28. oktober 2024 | 47 |
| 27. oktober 2024 | 53 |
| 26. oktober 2024 | 53 |
| 25. oktober 2024 | 54 |
| 24. oktober 2024 | 51 |