GMP Supporter
Denne stilling er desværre ikke længere ledig.
Se alle ledige stillinger
Hillerød
Would you like to contribute to ensuring a sky-high level of quality in the production of life-saving medicine? Do you dream of using your analytical approach to tasks? Are you keen on preparing documentation subject to strict compliance requirements? Then you will thrive as our new GMP Supporter. Apply today for a life-changing career!
The Position As a GMP Supporter, you will be responsible for various tasks, such as providing efficient and comprehensive support to the production lines, handle deviations and customer complaints, review batch documentation, and perform Standard Operation Procedure (SOP) updates and optimization projects. We are sitting in an open-plan office, where everyone is ready to lend a hand if there are challenges in meeting deadlines or if professional collaboration and input are needed. After some time, you will join colleagues in participating a phone duty approximately every 8 weeks. We are available 24/7 if there is a need from the production and we provide guidance in case of any quality issues. Qualifications The qualifications we value include: holding a minimum of bachelor’s degree in pharmacy, chemical engineering, biochemistry or similar, having an interest in being on the front line and helping colleagues with challenges across the organization and the ability to prepare documentation respecting a very high standard of quality. Since we have very close daily collaboration with operators and our quality department, it is essential that you write and speak fluent Danish and English. On a personal level, you quickly gain an overview of complex processes and solve issues in a systematic and data-driven manner. Amazing communication skills enable you to express concisely when documenting events related to the production lines . Taking the lead, maintaining responsibility and initiative in solving challenges to improve the production line is crucial in this role. Being a team player, who meets deadlines while ensuring our quality is uncompromised, while thriving on following procedures and adhering to standards are key to succeed in this team. About the department The department is part of Injectable Finished Products (IFP) consisting of approximately 190 employees divided into 9 teams, ensuring the production and release of a range of different products for patients worldwide.
The department is rapidly evolving, the pace is high, and therefore it is important that you thrive in a dynamic environment.
You will join one of our two Quality Support teams, comprised of highly committed employees who support our three packaging lines regarding quality challenges, batch documentation review, and minor optimization projects. Working at 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 building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energize us to perform our best at work.
Contact For further information, please contact Associate Manager Julie Agerschou via email: Deadline 14 April 2024. 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.
The Position As a GMP Supporter, you will be responsible for various tasks, such as providing efficient and comprehensive support to the production lines, handle deviations and customer complaints, review batch documentation, and perform Standard Operation Procedure (SOP) updates and optimization projects. We are sitting in an open-plan office, where everyone is ready to lend a hand if there are challenges in meeting deadlines or if professional collaboration and input are needed. After some time, you will join colleagues in participating a phone duty approximately every 8 weeks. We are available 24/7 if there is a need from the production and we provide guidance in case of any quality issues. Qualifications The qualifications we value include: holding a minimum of bachelor’s degree in pharmacy, chemical engineering, biochemistry or similar, having an interest in being on the front line and helping colleagues with challenges across the organization and the ability to prepare documentation respecting a very high standard of quality. Since we have very close daily collaboration with operators and our quality department, it is essential that you write and speak fluent Danish and English. On a personal level, you quickly gain an overview of complex processes and solve issues in a systematic and data-driven manner. Amazing communication skills enable you to express concisely when documenting events related to the production lines . Taking the lead, maintaining responsibility and initiative in solving challenges to improve the production line is crucial in this role. Being a team player, who meets deadlines while ensuring our quality is uncompromised, while thriving on following procedures and adhering to standards are key to succeed in this team. About the department The department is part of Injectable Finished Products (IFP) consisting of approximately 190 employees divided into 9 teams, ensuring the production and release of a range of different products for patients worldwide.
The department is rapidly evolving, the pace is high, and therefore it is important that you thrive in a dynamic environment.
You will join one of our two Quality Support teams, comprised of highly committed employees who support our three packaging lines regarding quality challenges, batch documentation review, and minor optimization projects. Working at 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 building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energize us to perform our best at work.
Contact For further information, please contact Associate Manager Julie Agerschou via email: Deadline 14 April 2024. 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.
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 20.3.2024, 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
Lignende jobs
-
Øvrige i Vedbæk
Få mere info- Øvrige
- Vedbæk
-
Øvrige i Rungsted Kyst
Få mere info- Øvrige
- Rungsted Kyst
-
Øvrige i Nivå
Få mere info- Øvrige
- Nivå
-
Øvrige i Værløse
Få mere info- Øvrige
- Værløse
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.
Se flere statistikker her:
Statistik over udbudte øvrige over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 26. april 2024 | 78 |
| 25. april 2024 | 73 |
| 24. april 2024 | 71 |
| 23. april 2024 | 69 |
| 22. april 2024 | 84 |
| 21. april 2024 | 83 |
| 20. april 2024 | 84 |
| 19. april 2024 | 82 |
| 18. april 2024 | 78 |
| 17. april 2024 | 76 |
| 16. april 2024 | 70 |
| 15. april 2024 | 81 |
| 14. april 2024 | 86 |
| 13. april 2024 | 84 |
| 12. april 2024 | 82 |
| 11. april 2024 | 80 |
| 10. april 2024 | 73 |
| 9. april 2024 | 68 |
| 8. april 2024 | 70 |
| 7. april 2024 | 80 |
| 6. april 2024 | 80 |
| 5. april 2024 | 77 |
| 4. april 2024 | 75 |
| 3. april 2024 | 76 |
| 2. april 2024 | 77 |
| 1. april 2024 | 84 |
| 31. marts 2024 | 87 |
| 30. marts 2024 | 87 |
| 29. marts 2024 | 91 |
| 28. marts 2024 | 86 |
| 27. marts 2024 | 86 |