Advanced QA Professional
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Gentofte
Do you get energized by many different responsibilities within a broad spectrum of tasks? Do you get motivated in a job where you work together with highly competent and helpful colleagues who jointly share the responsibility to secure the quality of Active Pharmaceutical Ingredients (API) production of biological medicine?
If yes, it’s the most perfect time to join our company and be part of a life-changing career! The position
The position is based our API production facility in Hillerød, which is not just a standard production facility, but one of the most interesting and challenging ones, as we not only produce API for marketed products but also run production for phase 3 clinical trials and process validation of new products about to be released.
As an Advanced QA Professional, you will use your talents to secure our running production as well handling complex new projects, as new equipment, new processes or completely new products.
Your overall responsibilities will be to:
• set the direction for quality and compliance based on the regulatory requirements we comply with
• ensure the solutions integrate quality and compliance with good optimizations in production
Qualifications To succeed in this role, you:
• hold a MSc in pharmacy, engineering, veterinary science, biotechnology or similar
• have several years of experience within the pharmaceutical industry, either from Production, Validation or Quality
• preferably have experience within Equipment Validation
• are fluent in English
On a personal level, you own a strong quality mindset and are able to thrive in an environment with different tasks, demonstrating solution-focused dialogue with both the production and your other QA colleagues.
You can communicate clearly and effectively with stakeholders, and keep a respectful tone, even when the message is not easy, contributing positively to a good overall working environment, and showing good collaboration skills with colleagues. About the department
We are a well-functioning department with many interfaces in the organization including production, management, and other QA departments. We love professional challenges, work with great individual responsibilities, have a high level of commitment and a good socializing environment, convinced that these ingredients make it an inspiring and fun place to work. All together we are 60 employees covering the production of API across our sites in Hillerød, Kalundborg and Gentofte. You will be part of the team with 16 colleagues based in Hillerød.
We can offer an exciting and challenging position, where you become part of a highly skilled team that acts as sparring partners and problem solvers within quality assurance issues for the production. 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 Nikolaj O. Christiansen, QA Associate Manager +45 3075 6771 Deadline
15 January 2024 We look forward to reading your application, and we will schedule interviews on an ongoing basis, so do not hesitate to apply as soon as possible. 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.
If yes, it’s the most perfect time to join our company and be part of a life-changing career! The position
The position is based our API production facility in Hillerød, which is not just a standard production facility, but one of the most interesting and challenging ones, as we not only produce API for marketed products but also run production for phase 3 clinical trials and process validation of new products about to be released.
As an Advanced QA Professional, you will use your talents to secure our running production as well handling complex new projects, as new equipment, new processes or completely new products.
Your overall responsibilities will be to:
• set the direction for quality and compliance based on the regulatory requirements we comply with
• ensure the solutions integrate quality and compliance with good optimizations in production
Qualifications To succeed in this role, you:
• hold a MSc in pharmacy, engineering, veterinary science, biotechnology or similar
• have several years of experience within the pharmaceutical industry, either from Production, Validation or Quality
• preferably have experience within Equipment Validation
• are fluent in English
On a personal level, you own a strong quality mindset and are able to thrive in an environment with different tasks, demonstrating solution-focused dialogue with both the production and your other QA colleagues.
You can communicate clearly and effectively with stakeholders, and keep a respectful tone, even when the message is not easy, contributing positively to a good overall working environment, and showing good collaboration skills with colleagues. About the department
We are a well-functioning department with many interfaces in the organization including production, management, and other QA departments. We love professional challenges, work with great individual responsibilities, have a high level of commitment and a good socializing environment, convinced that these ingredients make it an inspiring and fun place to work. All together we are 60 employees covering the production of API across our sites in Hillerød, Kalundborg and Gentofte. You will be part of the team with 16 colleagues based in Hillerød.
We can offer an exciting and challenging position, where you become part of a highly skilled team that acts as sparring partners and problem solvers within quality assurance issues for the production. 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 Nikolaj O. Christiansen, QA Associate Manager +45 3075 6771 Deadline
15 January 2024 We look forward to reading your application, and we will schedule interviews on an ongoing basis, so do not hesitate to apply as soon as possible. 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 Gentofte.
Jobbet er oprettet på vores service den 27.10.2023, 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
- Gentofte
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Statistik over udbudte jobs som øvrige i Gentofte
Herunder ser du udviklingen i udbudte øvrige i Gentofte 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 i Gentofte over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 2. juli 2024 | 17 |
| 1. juli 2024 | 17 |
| 30. juni 2024 | 20 |
| 29. juni 2024 | 20 |
| 28. juni 2024 | 17 |
| 27. juni 2024 | 20 |
| 26. juni 2024 | 22 |
| 25. juni 2024 | 20 |
| 24. juni 2024 | 20 |
| 23. juni 2024 | 24 |
| 22. juni 2024 | 24 |
| 21. juni 2024 | 21 |
| 20. juni 2024 | 20 |
| 19. juni 2024 | 21 |
| 18. juni 2024 | 20 |
| 17. juni 2024 | 20 |
| 16. juni 2024 | 23 |
| 15. juni 2024 | 23 |
| 14. juni 2024 | 22 |
| 13. juni 2024 | 21 |
| 12. juni 2024 | 22 |
| 11. juni 2024 | 20 |
| 10. juni 2024 | 21 |
| 9. juni 2024 | 24 |
| 8. juni 2024 | 24 |
| 7. juni 2024 | 25 |
| 6. juni 2024 | 23 |
| 5. juni 2024 | 22 |
| 4. juni 2024 | 21 |
| 3. juni 2024 | 21 |
| 2. juni 2024 | 21 |