Quality Assurance Professional with focus on simplifying and optimizing processes in FP production
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Kalundborg
Would you like to be part of an exciting innovation journey to implement new production lines at Novo Nordisk? Do you have a strong quality mind-set and great interpersonal skills to make a difference within Quality Assurance? Then there is a challenging job opportunity in Injectable Finished Products (IFP) QA at Kalundborg, Denmark.
We can offer a great working environment with high level of team spirit as well as highly skilled, ambitious, and engaged colleagues. We offer an exciting job opportunity that will match your experience. We are looking for a professional like you with a high level of dedication, and an innovative mindset, who thrives in a constantly changing and challenging environment.
The Position
You will be part of the QA FP daily operation team. Your main responsibility will be approval and document review of several different types of documents as well as QA oversight of processes related to the daily operation of an assembly and packaging facility in Kalundborg. You will spend time being present on shopfloor in the production as a consultant to support solving issues in real time, as well as improving and simplifying processes. Our purpose is to ensure high product quality and compliance with the current GMP rules and guidelines.
QA is a major player at internal audits and external authority inspections where you will be expected to participate and present data if needed.
Qualifications
We seek a colleague who fits our team both professionally and personally. As a person you are open minded, honest and inclusive regarding your colleagues in both QA and the production.
• You hold an academic degree within Ms. Pharmacy, veterinarian or similar, this to ensure you fulfil the requirements from the Danish Medicine Agency to “Qualified Person”.
• Preferably you have experience within the pharmaceutical industry. 2-3 years of experience with quality assurance and/or production as well as the right quality mindset will be an advantage.
• You are ambitious and ready to be part of our on-going effort to improve our high standards.
• You dare to challenge us in our way of working and has a desire to take initiative as well as being responsible for your own learning.
• You are a dedicated team player who inspires trust and respect among colleagues and partners.
• We are cooperating broadly with many stakeholders across different nationalities and therefore excellent collaboration and communication skills are needed.
• We operate in an international company and the position therefore requires proficiency in English and Danish. About the department
Our Quality assurance department consist of approx. 25 dedicated employees being responsible for assuring quality and compliance of FP operations and support the business by improving and simplifying processes. Our department releases products from Novo Nordisk to countries worldwide.
Working at Novo Nordisk
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronic diseases. In exchange, 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 Associate manager Lars Høg Mittag (+45 30795194).
We will conduct interviews continually.
Deadline
Deadline to apply for this position is March 8th 2023.
Applications will be considered on an ongoing basis.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
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.
We can offer a great working environment with high level of team spirit as well as highly skilled, ambitious, and engaged colleagues. We offer an exciting job opportunity that will match your experience. We are looking for a professional like you with a high level of dedication, and an innovative mindset, who thrives in a constantly changing and challenging environment.
The Position
You will be part of the QA FP daily operation team. Your main responsibility will be approval and document review of several different types of documents as well as QA oversight of processes related to the daily operation of an assembly and packaging facility in Kalundborg. You will spend time being present on shopfloor in the production as a consultant to support solving issues in real time, as well as improving and simplifying processes. Our purpose is to ensure high product quality and compliance with the current GMP rules and guidelines.
QA is a major player at internal audits and external authority inspections where you will be expected to participate and present data if needed.
Qualifications
We seek a colleague who fits our team both professionally and personally. As a person you are open minded, honest and inclusive regarding your colleagues in both QA and the production.
• You hold an academic degree within Ms. Pharmacy, veterinarian or similar, this to ensure you fulfil the requirements from the Danish Medicine Agency to “Qualified Person”.
• Preferably you have experience within the pharmaceutical industry. 2-3 years of experience with quality assurance and/or production as well as the right quality mindset will be an advantage.
• You are ambitious and ready to be part of our on-going effort to improve our high standards.
• You dare to challenge us in our way of working and has a desire to take initiative as well as being responsible for your own learning.
• You are a dedicated team player who inspires trust and respect among colleagues and partners.
• We are cooperating broadly with many stakeholders across different nationalities and therefore excellent collaboration and communication skills are needed.
• We operate in an international company and the position therefore requires proficiency in English and Danish. About the department
Our Quality assurance department consist of approx. 25 dedicated employees being responsible for assuring quality and compliance of FP operations and support the business by improving and simplifying processes. Our department releases products from Novo Nordisk to countries worldwide.
Working at Novo Nordisk
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronic diseases. In exchange, 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 Associate manager Lars Høg Mittag (+45 30795194).
We will conduct interviews continually.
Deadline
Deadline to apply for this position is March 8th 2023.
Applications will be considered on an ongoing basis.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
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 Kalundborg.
Jobbet er oprettet på vores service den 27.1.2023, 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
- Kalundborg
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Statistik over udbudte øvrige over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 26. april 2024 | 79 |
| 25. april 2024 | 77 |
| 24. april 2024 | 78 |
| 23. april 2024 | 76 |
| 22. april 2024 | 81 |
| 21. april 2024 | 80 |
| 20. april 2024 | 80 |
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| 18. april 2024 | 65 |
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| 15. april 2024 | 70 |
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| 8. april 2024 | 67 |
| 7. april 2024 | 74 |
| 6. april 2024 | 74 |
| 5. april 2024 | 73 |
| 4. april 2024 | 72 |
| 3. april 2024 | 68 |
| 2. april 2024 | 69 |
| 1. april 2024 | 69 |
| 31. marts 2024 | 75 |
| 30. marts 2024 | 75 |
| 29. marts 2024 | 73 |
| 28. marts 2024 | 70 |
| 27. marts 2024 | 71 |