Cleaning Scientist
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Kalundborg
Would you like to bring your expertise to the next level? Do you dream about joining a dynamic global company and work on an exciting new project? Are you interested in the opportunity to establish a factory that bridges new and automated technologies with strong know-how and expertise in biotech manufacturing?
Then you might be our new Cleaning Scientist! Apply today for a life-changing career!
The PositionAs a Cleaning Scientist, you will participate in project activities for investigating design, constructability, schedule and cost for a new purification facility. The key design principle will be to implement the best-in-class design standards from other facilities.This position offers an exciting chance to collaborate with different stakeholders from various levels, both internally and externally.Active participation in a skilled user organization is integral part of this role, fostering collaboration with engineering partners and contractors while overseeing their activities.Proactive management of project risks is vital for us, alongside the development of standards to ensure structure and transparency.Maintaining a team's focus on implementing established solutions is emphasized, with opportunities to contribute to the development of innovative design solutions where applicable.We are open to adjusting the tasks and the level of the position to your experience.The main tasks will be to:
• Participate in project activities such as design review, design risk assessments, Factory Acceptance Test (FAT) and Site Acceptance Testing (SAT).
• Perform test and documentation.
• Ensure validation of Cleaning-in-Place (CIP) of all process equipment, including ownership of CIP specific processes.
• Manage stakeholders.
QualificationsTo succeed in this role, you have:
• Minimum a bachelor’s degree in natural science.
• At least 3 years of experience in Good Manufacturing Practice (GMP) and ideally Active Pharmaceutical Ingredient (API) manufacturing.
• A solid understanding of unit operations, pharmaceutical processes and documentation.
• Knowledge and experience related to design review and validation of CIP, which is considered a plus.
• Full professional proficiency in verbal and written English.As a person, you enjoy close teamwork, can ride out a storm, and are a motivator for others. Thriving in a multicultural environment is your second nature, with the capability to make independent, critical decisions.Having a natural aptitude for building structure, which is complemented by a commitment to achieving simplicity is crucial in this role. While having great stakeholder management and problem-solving skills sets us up for success of this team, the ability to communicate with a variety of stakeholders is still the key to succeed.We will welcome a colleague whose motivation to succeed is paired with a strong determination to establish a clear and focused direction.You will be joining PS API Expansions The area is anchored in Product Supply, Quality & IT, which employs approximately 35,000 of ’s 64,000 employees globally.PS API Expansions is a growing area with the responsibility to design, plan and build all major API Expansions projects across to serve the needs of millions of patients.We build and design our future API facilities as multi-product facilities with the flexibility to accommodate future processes and display a state-of-the-art technology and working environment. We focus on delivering the highest quality to patients worldwide in an efficient and environmentally sustainable way.We are setting the standards for the future, designing facilities we will still be proud of many decades from now. We drive world-class execution of capacity projects, and together we build the future of .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 , life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.Contact For further information, please contact Project Associate Manager, Cleaning Mette Mulbjerg at +or via email at 20 April 2025.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 our new Cleaning Scientist! Apply today for a life-changing career!
The PositionAs a Cleaning Scientist, you will participate in project activities for investigating design, constructability, schedule and cost for a new purification facility. The key design principle will be to implement the best-in-class design standards from other facilities.This position offers an exciting chance to collaborate with different stakeholders from various levels, both internally and externally.Active participation in a skilled user organization is integral part of this role, fostering collaboration with engineering partners and contractors while overseeing their activities.Proactive management of project risks is vital for us, alongside the development of standards to ensure structure and transparency.Maintaining a team's focus on implementing established solutions is emphasized, with opportunities to contribute to the development of innovative design solutions where applicable.We are open to adjusting the tasks and the level of the position to your experience.The main tasks will be to:
• Participate in project activities such as design review, design risk assessments, Factory Acceptance Test (FAT) and Site Acceptance Testing (SAT).
• Perform test and documentation.
• Ensure validation of Cleaning-in-Place (CIP) of all process equipment, including ownership of CIP specific processes.
• Manage stakeholders.
QualificationsTo succeed in this role, you have:
• Minimum a bachelor’s degree in natural science.
• At least 3 years of experience in Good Manufacturing Practice (GMP) and ideally Active Pharmaceutical Ingredient (API) manufacturing.
• A solid understanding of unit operations, pharmaceutical processes and documentation.
• Knowledge and experience related to design review and validation of CIP, which is considered a plus.
• Full professional proficiency in verbal and written English.As a person, you enjoy close teamwork, can ride out a storm, and are a motivator for others. Thriving in a multicultural environment is your second nature, with the capability to make independent, critical decisions.Having a natural aptitude for building structure, which is complemented by a commitment to achieving simplicity is crucial in this role. While having great stakeholder management and problem-solving skills sets us up for success of this team, the ability to communicate with a variety of stakeholders is still the key to succeed.We will welcome a colleague whose motivation to succeed is paired with a strong determination to establish a clear and focused direction.You will be joining PS API Expansions The area is anchored in Product Supply, Quality & IT, which employs approximately 35,000 of ’s 64,000 employees globally.PS API Expansions is a growing area with the responsibility to design, plan and build all major API Expansions projects across to serve the needs of millions of patients.We build and design our future API facilities as multi-product facilities with the flexibility to accommodate future processes and display a state-of-the-art technology and working environment. We focus on delivering the highest quality to patients worldwide in an efficient and environmentally sustainable way.We are setting the standards for the future, designing facilities we will still be proud of many decades from now. We drive world-class execution of capacity projects, and together we build the future of .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 , life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.Contact For further information, please contact Project Associate Manager, Cleaning Mette Mulbjerg at +or via email at 20 April 2025.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 Kalundborg.
Jobbet er oprettet på vores service den 2.4.2025, 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.
- 02.04.2025
- Øvrige
- Kalundborg
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Statistik over udbudte jobs som øvrige i Kalundborg
Herunder ser du udviklingen i udbudte øvrige i Kalundborg 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.
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Statistik over udbudte jobs som øvrige i Kalundborg over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 24. april 2025 | 31 |
| 23. april 2025 | 32 |
| 22. april 2025 | 32 |
| 21. april 2025 | 39 |
| 20. april 2025 | 40 |
| 19. april 2025 | 40 |
| 18. april 2025 | 41 |
| 17. april 2025 | 40 |
| 16. april 2025 | 40 |
| 15. april 2025 | 39 |
| 14. april 2025 | 39 |
| 13. april 2025 | 44 |
| 12. april 2025 | 44 |
| 11. april 2025 | 46 |
| 10. april 2025 | 43 |
| 9. april 2025 | 41 |
| 8. april 2025 | 39 |
| 7. april 2025 | 38 |
| 6. april 2025 | 40 |
| 5. april 2025 | 40 |
| 4. april 2025 | 40 |
| 3. april 2025 | 53 |
| 2. april 2025 | 53 |
| 1. april 2025 | 45 |
| 31. marts 2025 | 45 |
| 30. marts 2025 | 49 |
| 29. marts 2025 | 49 |
| 28. marts 2025 | 46 |
| 27. marts 2025 | 45 |
| 26. marts 2025 | 39 |
| 25. marts 2025 | 36 |