Advanced 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 and be at the steering wheel when it comes to getting products to patients? If yes, we hope that you would like to become our new Project Quality Professional! The Position
The Project Quality Professional is a newly established position and will partner up with a Project Manager to standardize and improve the way validation activities are being conducted on sites globally as part of the Fill & Finish Expansions Project. The ideal candidate should possess validation and LEAN knowledge and take the lead in improving the standardized approach to validation activities 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:
• Act as product owner of the generic validation schedule, the standardized validation setup.
• Support stakeholders across the world in adapting and comply with the standard.
• Keep track of progression and capture lessons learned from site execution.
• Involve key stakeholders in identifying and implementing improvements. 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
• Experience from the pharmaceutical industry, preferably from working in production or as QA for production.
• Experience in execution of qualification/validation activities of processes/equipment.
• Strong communication skills in English, both written and spoken . As a person, you should possess and have a reputation for excellent collaboration skills. You 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. You will be joining Fill & Finish Expansions. The area is anchored in Product Supply, Quality & IT, which globally employ approximately 28,500 employees. Fill & Finish Expansions is a newly established and growing area with the responsibility to design, plan and build all major fill & finish expansion projects across PSQIT to serve the needs of millions of patients. We do it by rethinking our fill & finish facilities with the use of modern technology. We are setting the standards for the future, designing facilities we will still be proud of many decades from now. Fill & Finish Expansions has a global approach, where you will be working with multiple sites and cultures across the world. Working at
is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at , we’re working toward something bigger than ourselves, and it’s a collective effort. Join us! Together, we go further. Together, we’re life changing. Contact
If you want to know more, please reach out to Associate Manager, Jakob Brade, on +or get to know us better by visiting Novo Nordisk Global Manufacturing Careers. Deadline
9 June 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 to 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 is a newly established position and will partner up with a Project Manager to standardize and improve the way validation activities are being conducted on sites globally as part of the Fill & Finish Expansions Project. The ideal candidate should possess validation and LEAN knowledge and take the lead in improving the standardized approach to validation activities 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:
• Act as product owner of the generic validation schedule, the standardized validation setup.
• Support stakeholders across the world in adapting and comply with the standard.
• Keep track of progression and capture lessons learned from site execution.
• Involve key stakeholders in identifying and implementing improvements. 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
• Experience from the pharmaceutical industry, preferably from working in production or as QA for production.
• Experience in execution of qualification/validation activities of processes/equipment.
• Strong communication skills in English, both written and spoken . As a person, you should possess and have a reputation for excellent collaboration skills. You 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. You will be joining Fill & Finish Expansions. The area is anchored in Product Supply, Quality & IT, which globally employ approximately 28,500 employees. Fill & Finish Expansions is a newly established and growing area with the responsibility to design, plan and build all major fill & finish expansion projects across PSQIT to serve the needs of millions of patients. We do it by rethinking our fill & finish facilities with the use of modern technology. We are setting the standards for the future, designing facilities we will still be proud of many decades from now. Fill & Finish Expansions has a global approach, where you will be working with multiple sites and cultures across the world. Working at
is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at , we’re working toward something bigger than ourselves, and it’s a collective effort. Join us! Together, we go further. Together, we’re life changing. Contact
If you want to know more, please reach out to Associate Manager, Jakob Brade, on +or get to know us better by visiting Novo Nordisk Global Manufacturing Careers. Deadline
9 June 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 to 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 23.5.2024, 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.
- 23.05.2024
- Øvrige
- Nordsjælland
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Statistik over udbudte øvrige i Nordsjælland over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 15. juni 2024 | 525 |
| 14. juni 2024 | 527 |
| 13. juni 2024 | 519 |
| 12. juni 2024 | 509 |
| 11. juni 2024 | 510 |
| 10. juni 2024 | 506 |
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| 6. juni 2024 | 516 |
| 5. juni 2024 | 501 |
| 4. juni 2024 | 504 |
| 3. juni 2024 | 545 |
| 2. juni 2024 | 543 |
| 1. juni 2024 | 554 |
| 31. maj 2024 | 557 |
| 30. maj 2024 | 565 |
| 29. maj 2024 | 552 |
| 28. maj 2024 | 558 |
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| 26. maj 2024 | 549 |
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