Filling professional
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Hillerød
Are you ready to take on new and exciting challenges as part of the Filling support team in DFP (Diabetes Finished Products)? Do you have a science degree, some experience from pharma and know what it takes to work in compliance with standard procedures in a GMP (Good Manufacturing Practice) regulated environment? If so, this is your opportunity to join the AP (Aseptic Processing) Expansion project at our site in Hillerød.
About the department
You will be part of a filling support team of 13 experienced and highly engaged process supporters who is responsible for validation, operation, and re-qualification of our two isolator filling lines. Our department manages our two filling lines as well as all related equipment and processes. Daily department activities include creating standards, validating processes and equipment, handling deviations, and ensuring that we have procedures in place for production. We work across departments and cultures and always strive to deliver best in class support to our customers.
The position
As a filling professional your responsibilities include optimising processes and procedures, deviation handling, project execution, validation activities and getting regulatory approvals, all in accordance with quality and compliance. As a facility we are developing new processes and optimizing daily work using cLEAN as our primary tool. The team consists of a wide range of competences which gives the right candidate opportunities to develop skills within a variety of fields of expertise. You will be involved in maintaining a prominent level of compliance and work with regulatory approvals of the filling equipment and processes by ensuring correct documentation and being always inspection ready. Qualifications You have a relevant science degree such as engineering, pharmaceutical or similar and at least a couple of years of experience in the medical industry. Preferably you have at least 2 years of experience within aseptic filling processes and equipment and have worked with processes in a cGMP environment. You understand the regulatory environment and ensuring compliance comes as second nature. You have worked with validation and documentation processes before and have experience with writing protocols, test plans, deviations, change request cases and SOPs (Standard Operating Procedures). You work in a structured manner, systematically with an eye for detail, with changing priorities and can manage hands-on tasks as well. Your hands-on experience has sharpened your already excellent communication and coordination skills and through your “can do” attitude you make things happen. You are highly skilled at communicating at all organizational levels - with operators, managers, and specialists - verbally as well as in writing. Finally, you have good skills in verbal and written English
Working at Novo Nordisk
At Novo Nordisk, we use our skills, dedication, and ambition to help people with diabetes. We offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development
Contact
For further information, please contact Steffen Elholm Andersen on +4530794709
Deadline 26 February 2023. You must submit your application in English. Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified. 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.
About the department
You will be part of a filling support team of 13 experienced and highly engaged process supporters who is responsible for validation, operation, and re-qualification of our two isolator filling lines. Our department manages our two filling lines as well as all related equipment and processes. Daily department activities include creating standards, validating processes and equipment, handling deviations, and ensuring that we have procedures in place for production. We work across departments and cultures and always strive to deliver best in class support to our customers.
The position
As a filling professional your responsibilities include optimising processes and procedures, deviation handling, project execution, validation activities and getting regulatory approvals, all in accordance with quality and compliance. As a facility we are developing new processes and optimizing daily work using cLEAN as our primary tool. The team consists of a wide range of competences which gives the right candidate opportunities to develop skills within a variety of fields of expertise. You will be involved in maintaining a prominent level of compliance and work with regulatory approvals of the filling equipment and processes by ensuring correct documentation and being always inspection ready. Qualifications You have a relevant science degree such as engineering, pharmaceutical or similar and at least a couple of years of experience in the medical industry. Preferably you have at least 2 years of experience within aseptic filling processes and equipment and have worked with processes in a cGMP environment. You understand the regulatory environment and ensuring compliance comes as second nature. You have worked with validation and documentation processes before and have experience with writing protocols, test plans, deviations, change request cases and SOPs (Standard Operating Procedures). You work in a structured manner, systematically with an eye for detail, with changing priorities and can manage hands-on tasks as well. Your hands-on experience has sharpened your already excellent communication and coordination skills and through your “can do” attitude you make things happen. You are highly skilled at communicating at all organizational levels - with operators, managers, and specialists - verbally as well as in writing. Finally, you have good skills in verbal and written English
Working at Novo Nordisk
At Novo Nordisk, we use our skills, dedication, and ambition to help people with diabetes. We offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development
Contact
For further information, please contact Steffen Elholm Andersen on +4530794709
Deadline 26 February 2023. You must submit your application in English. Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified. 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 Hillerød.
Jobbet er oprettet på vores service den 9.2.2023, 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
- Hillerød
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Statistik over udbudte øvrige over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 13. maj 2024 | 82 |
| 12. maj 2024 | 86 |
| 11. maj 2024 | 86 |
| 10. maj 2024 | 82 |
| 9. maj 2024 | 86 |
| 8. maj 2024 | 83 |
| 7. maj 2024 | 76 |
| 6. maj 2024 | 80 |
| 5. maj 2024 | 77 |
| 4. maj 2024 | 78 |
| 3. maj 2024 | 68 |
| 2. maj 2024 | 69 |
| 1. maj 2024 | 73 |
| 30. april 2024 | 74 |
| 29. april 2024 | 70 |
| 28. april 2024 | 81 |
| 27. april 2024 | 82 |
| 26. april 2024 | 78 |
| 25. april 2024 | 73 |
| 24. april 2024 | 71 |
| 23. april 2024 | 69 |
| 22. april 2024 | 84 |
| 21. april 2024 | 83 |
| 20. april 2024 | 84 |
| 19. april 2024 | 82 |
| 18. april 2024 | 78 |
| 17. april 2024 | 76 |
| 16. april 2024 | 70 |
| 15. april 2024 | 81 |
| 14. april 2024 | 86 |
| 13. april 2024 | 84 |