Senior IT QA Professional for Validation Projects
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Nordsjælland
Is it your dream to work for an international expansion project? Are you motivated to make a difference? Is continuous development and growth the key to your satisfaction?
Then you might be the Senior IT QA Professional we are looking for to support the establishment of our new aseptic production and warehouse facilities across the world. Apply today and join us for a life-changing career!
The position
is establishing new, ground-breaking biotech facilities and factories utilising modern technology with fully automated operations and digitalised processes globally.
As a Senior IT QA Professional, you will be part of a global project, working with the project team in delivering best-in-class quality for qualification of pharmaceutical aseptic facilities, warehouses, IT/OT systems, equipment, and processes in line with the science and risk-based validation principles.
You will be responsible for: • Providing direction and oversight for quality assurance in one or more aseptic production and warehouse processes • Approving documentation and conducting QA oversight of IT/OT validation activities This role will allow you to work with stakeholders across the organisation and globe. Thus, international travelling is to be expected monthly.
We offer a flexible work schedule that allows you to plan your daily tasks and occasionally work from home when suitable for the operation and your team needs.
provides various opportunities for professional growth and impactful achievements. You will have various possibilities to contribute to an exciting growth journey within Fill & Finish Expansions QA Project, ensuring product quality and patient safety. As a Senior IT QA Professional, you will have the chance to develop competencies, broaden your knowledge and skills and make a significant impact on the organization.
Qualifications
We are seeking an individual with excellent skills in collaborating with stakeholders from different organisational levels and diverse cultures, possessing a strong quality mindset and a result-oriented approach. To thrive and succeed in this role, you have: • Bachelor or Master’s degree (could be pharmacy, chemical engineering, natural sciences or similar) • Several years of experience working in a GMP regulated environment • Several years of experience working with validation of IT and OT systems within pharmaceutical production • Proficiency in spoken and written English Moreover, it is an advantage if you have experience from a Quality Assurance role as well as knowledge within intralogistics and warehousing and/or aseptic production.
As a person you are positive, cooperative, detail, and solution oriented, and you work systematically, logically, and proactively. You present a risk-based approach and the ability to balance compliance and product quality.
Additionally, you thrive in a dynamic environment where cooperation with many different stakeholders will be crucial to your success.
About the department
Fill & Finish Expansions QA Project belongs in the newly established Fill & Finish Expansions area. The new area is working to increase the aseptic production and warehouse capacity across the network to ensure we continue to deliver high quality products for our patients, also in the future.
Our department has a global responsibility for quality assurance and compliance of the new facilities. We ensure a high level of quality and compliance with GMP in close cooperation with our stakeholders. And we have an international collaboration with local QA for the new facilities.
You will be part of a team and a department that works in a vibrant and positive working environment and values exchange of knowledge and experience. Networking and cooperation are key to our success.
Working at
At , 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, please contact Morten Vermehren Jensen, Manager at +.
Deadline
12 November 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.
Then you might be the Senior IT QA Professional we are looking for to support the establishment of our new aseptic production and warehouse facilities across the world. Apply today and join us for a life-changing career!
The position
is establishing new, ground-breaking biotech facilities and factories utilising modern technology with fully automated operations and digitalised processes globally.
As a Senior IT QA Professional, you will be part of a global project, working with the project team in delivering best-in-class quality for qualification of pharmaceutical aseptic facilities, warehouses, IT/OT systems, equipment, and processes in line with the science and risk-based validation principles.
You will be responsible for: • Providing direction and oversight for quality assurance in one or more aseptic production and warehouse processes • Approving documentation and conducting QA oversight of IT/OT validation activities This role will allow you to work with stakeholders across the organisation and globe. Thus, international travelling is to be expected monthly.
We offer a flexible work schedule that allows you to plan your daily tasks and occasionally work from home when suitable for the operation and your team needs.
provides various opportunities for professional growth and impactful achievements. You will have various possibilities to contribute to an exciting growth journey within Fill & Finish Expansions QA Project, ensuring product quality and patient safety. As a Senior IT QA Professional, you will have the chance to develop competencies, broaden your knowledge and skills and make a significant impact on the organization.
Qualifications
We are seeking an individual with excellent skills in collaborating with stakeholders from different organisational levels and diverse cultures, possessing a strong quality mindset and a result-oriented approach. To thrive and succeed in this role, you have: • Bachelor or Master’s degree (could be pharmacy, chemical engineering, natural sciences or similar) • Several years of experience working in a GMP regulated environment • Several years of experience working with validation of IT and OT systems within pharmaceutical production • Proficiency in spoken and written English Moreover, it is an advantage if you have experience from a Quality Assurance role as well as knowledge within intralogistics and warehousing and/or aseptic production.
As a person you are positive, cooperative, detail, and solution oriented, and you work systematically, logically, and proactively. You present a risk-based approach and the ability to balance compliance and product quality.
Additionally, you thrive in a dynamic environment where cooperation with many different stakeholders will be crucial to your success.
About the department
Fill & Finish Expansions QA Project belongs in the newly established Fill & Finish Expansions area. The new area is working to increase the aseptic production and warehouse capacity across the network to ensure we continue to deliver high quality products for our patients, also in the future.
Our department has a global responsibility for quality assurance and compliance of the new facilities. We ensure a high level of quality and compliance with GMP in close cooperation with our stakeholders. And we have an international collaboration with local QA for the new facilities.
You will be part of a team and a department that works in a vibrant and positive working environment and values exchange of knowledge and experience. Networking and cooperation are key to our success.
Working at
At , 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, please contact Morten Vermehren Jensen, Manager at +.
Deadline
12 November 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 29.10.2024, 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.
- 29.10.2024
- Øvrige
- Nordsjælland
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Statistik over udbudte jobs som øvrige i Nordsjælland
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Statistik over udbudte øvrige i Nordsjælland over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 21. november 2024 | 396 |
| 20. november 2024 | 404 |
| 19. november 2024 | 395 |
| 18. november 2024 | 383 |
| 17. november 2024 | 396 |
| 16. november 2024 | 401 |
| 15. november 2024 | 409 |
| 14. november 2024 | 406 |
| 13. november 2024 | 394 |
| 12. november 2024 | 392 |
| 11. november 2024 | 395 |
| 10. november 2024 | 402 |
| 9. november 2024 | 407 |
| 8. november 2024 | 401 |
| 7. november 2024 | 410 |
| 6. november 2024 | 403 |
| 5. november 2024 | 393 |
| 4. november 2024 | 401 |
| 3. november 2024 | 403 |
| 2. november 2024 | 405 |
| 1. november 2024 | 417 |
| 31. oktober 2024 | 418 |
| 30. oktober 2024 | 407 |
| 29. oktober 2024 | 415 |
| 28. oktober 2024 | 431 |
| 27. oktober 2024 | 440 |
| 26. oktober 2024 | 443 |
| 25. oktober 2024 | 425 |
| 24. oktober 2024 | 427 |
| 23. oktober 2024 | 552 |
| 22. oktober 2024 | 575 |