Project Quality Professional
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Nordsjælland
Are you skilled within GMP and do you like to work in an exciting project environment? Do you want to be a part of initiatives where quality is a priority? Then we hope that you would like to become our new Project Quality Professional, we are seeking more than one candidate! The position
The Project Quality Professional will be responsible for implementing standardized qualification processes on sites globally as part of the Fill & Finish Expansions Project. The ideal candidate should possess production and validation knowledge and take the lead in setting the direction based on best practices and extensive collaboration with sites worldwide. Although the role will be based in Denmark, it will integrate with the project organizations at our global sites.
The key responsibilities of this position include: Implementing standardized project quality processes for the Fill & Finish Expansions Project Preparing a standard validation execution setup using a Science and Risk-based Validation (SRV) approach Communicating with counterparts around the world
Qualifications To be successful in this role, you should meet the following qualifications: Relevant academic education, such as production, chemical or process engineering, pharmacy, biology, microbiology, or equivalent Some experience in the pharmaceutical industry, preferably from working in production or as QA for production Experience in qualification/validation of processes/equipment or experience with it compliance or automation We are recruiting for multiple positions, and therefore, we are flexible regarding the level of experience of the candidates. In addition, the ideal candidate for this role should possess strong communication skills in English, both written and spoken, and have a reputation for excellent collaboration skills. They should have a determined approach to taking the lead on tasks and be enthusiastic about facing new challenges and learning new things. About the department
The Validation Standards department at is responsible for developing a global validation standard for all new Fill Finish facilities sites, ensuring the quality of the final product during the manufacturing process. We develop and implement quality control plans and work closely with other departments to maintain quality standards. The department is staffed with highly qualified professionals and specialists who continuously develop and improve quality control processes from design to final validation.
Working at
is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. relies on the joint potential and collaboration of its more than 50,000 employees. Together, we go further. Together, we’re life changing. Contact
For further information, please contact Lene Højgaard Christensen, Senior manager Quality Planning at +. Deadline
1 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 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 Project Quality Professional will be responsible for implementing standardized qualification processes on sites globally as part of the Fill & Finish Expansions Project. The ideal candidate should possess production and validation knowledge and take the lead in setting the direction based on best practices and extensive collaboration with sites worldwide. Although the role will be based in Denmark, it will integrate with the project organizations at our global sites.
The key responsibilities of this position include:
Qualifications To be successful in this role, you should meet the following qualifications:
The Validation Standards department at is responsible for developing a global validation standard for all new Fill Finish facilities sites, ensuring the quality of the final product during the manufacturing process. We develop and implement quality control plans and work closely with other departments to maintain quality standards. The department is staffed with highly qualified professionals and specialists who continuously develop and improve quality control processes from design to final validation.
Working at
is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. relies on the joint potential and collaboration of its more than 50,000 employees. Together, we go further. Together, we’re life changing. Contact
For further information, please contact Lene Højgaard Christensen, Senior manager Quality Planning at +. Deadline
1 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 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 Nordsjælland
Jobbet er oprettet på vores service den 30.1.2024, 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.
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Statistik over udbudte øvrige i Nordsjælland over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 26. april 2024 | 537 |
| 25. april 2024 | 531 |
| 24. april 2024 | 515 |
| 23. april 2024 | 530 |
| 22. april 2024 | 540 |
| 21. april 2024 | 534 |
| 20. april 2024 | 534 |
| 19. april 2024 | 530 |
| 18. april 2024 | 532 |
| 17. april 2024 | 516 |
| 16. april 2024 | 511 |
| 15. april 2024 | 524 |
| 14. april 2024 | 540 |
| 13. april 2024 | 532 |
| 12. april 2024 | 537 |
| 11. april 2024 | 533 |
| 10. april 2024 | 534 |
| 9. april 2024 | 518 |
| 8. april 2024 | 518 |
| 7. april 2024 | 548 |
| 6. april 2024 | 552 |
| 5. april 2024 | 548 |
| 4. april 2024 | 539 |
| 3. april 2024 | 540 |
| 2. april 2024 | 529 |
| 1. april 2024 | 561 |
| 31. marts 2024 | 589 |
| 30. marts 2024 | 588 |
| 29. marts 2024 | 596 |
| 28. marts 2024 | 601 |
| 27. marts 2024 | 606 |