Quality Assurance Professional
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Kalundborg
Do you like to have impact on decisions? Are you able to ensure compliance and high quality in your job? Would you thrive by working with skilled colleagues known for their fantastic team spirit? If so then come work with us in Kalundborg. The position
In close cooperation with colleagues, you will act as a QA Professional in Biotech and Rare Disease department. Thereby ensuring that the products are of high standards and in full compliance with the current rules and guidelines. We are offering an exciting and flexible job where you will be part of a competent and well-functioning team. Your main responsibilities will be: To review batch documentation, batch related documentation from support processes, trend reports, Standard Operating Procedures (SOPs) and deviations. To observe performed processes and help solve issues in real time. Advising stakeholders to ensure the right level of quality in the production processes. Taking on the role as Qualified Person delegate (QPd). Participating and presenting cases when we are inspected by authorities from around the world. Improve processes in your working area. Qualifications
To succeed in this role you should have: A Master’s degree in pharmacy, medicine, microbiology, veterinary medicine or similar. 1 year of experience within QA or other relevant production related job would be advantageous. Knowledge of Good Manufacturing Practice (GMP) and regulations. Strong communication skills with stakeholders, maintaining a respectful tone. Proficiency in Danish and English, along with good IT skills. As a person, you possess a keen eye for detail and are naturally engaged. You excel in establishing strong relations with stakeholders, making you an asset to our team both personally and professionally. About the department
Biotech and Rare Disease Quality Assurance Finished Products in Kalundborg is a well-functioning department with many interfaces in the organization including production, management, and other QA departments. We are 60 engaged employees with a great team spirit, and we overcome obstacles with open and honest communication. We love professional challenges, working with individual responsibilities, and have one of the best places to work and grow. Our main task is to help set and ensure the quality direction of our production area, thereby having direct impact on products delivered to patients all over the world. Meaning, our QA role is to advice and confirm to ensure our production is in compliance with internal and external guidelines at all times. Working at Novo Nordisk
At Novo Nordisk, we use our competencies, dedication, and ambitions to help many people improve their lives. At the same time, we offer the opportunity to become part of a global workplace where you work with talented colleagues and where your passion and commitment are met with opportunities for personal and professional development. Contact
If you have any questions, you are welcome to contact Manager Charlotte Johnsson on +45 3075 9470. 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 / CV. You may submit your application in English or in Danish. We will review applications received on an ongoing basis, so do not hesitate to apply as soon as possible. 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.
In close cooperation with colleagues, you will act as a QA Professional in Biotech and Rare Disease department. Thereby ensuring that the products are of high standards and in full compliance with the current rules and guidelines. We are offering an exciting and flexible job where you will be part of a competent and well-functioning team. Your main responsibilities will be:
To succeed in this role you should have:
Biotech and Rare Disease Quality Assurance Finished Products in Kalundborg is a well-functioning department with many interfaces in the organization including production, management, and other QA departments. We are 60 engaged employees with a great team spirit, and we overcome obstacles with open and honest communication. We love professional challenges, working with individual responsibilities, and have one of the best places to work and grow. Our main task is to help set and ensure the quality direction of our production area, thereby having direct impact on products delivered to patients all over the world. Meaning, our QA role is to advice and confirm to ensure our production is in compliance with internal and external guidelines at all times. Working at Novo Nordisk
At Novo Nordisk, we use our competencies, dedication, and ambitions to help many people improve their lives. At the same time, we offer the opportunity to become part of a global workplace where you work with talented colleagues and where your passion and commitment are met with opportunities for personal and professional development. Contact
If you have any questions, you are welcome to contact Manager Charlotte Johnsson on +45 3075 9470. 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 / CV. You may submit your application in English or in Danish. We will review applications received on an ongoing basis, so do not hesitate to apply as soon as possible. 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 29.5.2024, 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.
- Øvrige
- Kalundborg
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Statistik over udbudte øvrige i Kalundborg over tid
Dato | Alle jobs som øvrige |
---|---|
22. november 2024 | 50 |
21. november 2024 | 52 |
20. november 2024 | 54 |
19. november 2024 | 50 |
18. november 2024 | 52 |
17. november 2024 | 58 |
16. november 2024 | 59 |
15. november 2024 | 58 |
14. november 2024 | 60 |
13. november 2024 | 56 |
12. november 2024 | 52 |
11. november 2024 | 54 |
10. november 2024 | 59 |
9. november 2024 | 59 |
8. november 2024 | 60 |
7. november 2024 | 57 |
6. november 2024 | 57 |
5. november 2024 | 57 |
4. november 2024 | 50 |
3. november 2024 | 52 |
2. november 2024 | 53 |
1. november 2024 | 53 |
31. oktober 2024 | 55 |
30. oktober 2024 | 52 |
29. oktober 2024 | 53 |
28. oktober 2024 | 51 |
27. oktober 2024 | 51 |
26. oktober 2024 | 52 |
25. oktober 2024 | 48 |
24. oktober 2024 | 49 |
23. oktober 2024 | 48 |
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