Quality Assurance Professional
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Gentofte
Do you have a background within pharmaceutical production? Do you get energized by many different responsibilities within a broad spectrum of tasks? Do you get motivated in a job where you work together with highly competent and helpful colleagues who jointly share the responsibility to secure the quality of API production of biological medicine? Then you have a great opportunity to become our new colleague in Biotech and Rare Disease, Gentofte.
The position
As QA Professional, you need to use your talents to release our products, and this requires us to do our utmost every day to ensure that we meet the ever-increasing demands of the authorities and thereby build proper quality into our processes.
As releasing QA Professional, it is our overall responsibility to set the direction for quality and compliance based on the regulatory requirements we comply with. You must therefore help to ensure the solutions that integrate quality and compliance with good optimizations in production. This requires good cooperation and a solution-focused dialogue with both the production and your other QA colleagues. We are always working on an effective review and approval process on cases from the production and our other core tasks to ensure that we get products out to our patients at the right quality and in a timely manner.
Qualifications As our new Quality Assurance Professional, the key requirements are:
• A degree in pharmacy, engineering within Life Science, veterinary science, or similar MSc to meet the Danish Medicines Agency's requirements
• Up to date GMP production experience
• Able to take on responsibilities, set high quality standards and ensure compliance, based on the regulatory requirements
• Able to use your competencies and talents to release our products
• Own a strong quality mindset
• Able to thrive in an environment with different tasks
• Able to communicate clearly and effectively with stakeholders, and keep a respectful tone, even when the message is not easy
• Contribute positively to a good overall working environment, and show good collaboration skills with colleagues
• Can demonstrate solution-focused dialogue with both the production and your other QA colleagues About the department
We are a well-functioning department with many interfaces in the organization including production, management, and other QA departments. We love professional challenges, work with great individual responsibilities, have a high level of commitment and a good socializing environment, convinced that these ingredients make it an inspiring and fun place to work. All together we are 60 employees covering the production of API across our sites in Hillerød, Kalundborg and Gentofte. You will be part of the team with 16 colleagues based in Gentofte.
We can offer an exciting and challenging position, where you become part of a highly skilled team that acts as sparring partners and problem solvers within quality assurance issues for the production. 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 For further information, you are welcome to contact Susan Aagaard, QA Associate Manager +45 30752712 Deadline
May 15, 2023 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 look forward to reading your application, and 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.
The position
As QA Professional, you need to use your talents to release our products, and this requires us to do our utmost every day to ensure that we meet the ever-increasing demands of the authorities and thereby build proper quality into our processes.
As releasing QA Professional, it is our overall responsibility to set the direction for quality and compliance based on the regulatory requirements we comply with. You must therefore help to ensure the solutions that integrate quality and compliance with good optimizations in production. This requires good cooperation and a solution-focused dialogue with both the production and your other QA colleagues. We are always working on an effective review and approval process on cases from the production and our other core tasks to ensure that we get products out to our patients at the right quality and in a timely manner.
Qualifications As our new Quality Assurance Professional, the key requirements are:
• A degree in pharmacy, engineering within Life Science, veterinary science, or similar MSc to meet the Danish Medicines Agency's requirements
• Up to date GMP production experience
• Able to take on responsibilities, set high quality standards and ensure compliance, based on the regulatory requirements
• Able to use your competencies and talents to release our products
• Own a strong quality mindset
• Able to thrive in an environment with different tasks
• Able to communicate clearly and effectively with stakeholders, and keep a respectful tone, even when the message is not easy
• Contribute positively to a good overall working environment, and show good collaboration skills with colleagues
• Can demonstrate solution-focused dialogue with both the production and your other QA colleagues About the department
We are a well-functioning department with many interfaces in the organization including production, management, and other QA departments. We love professional challenges, work with great individual responsibilities, have a high level of commitment and a good socializing environment, convinced that these ingredients make it an inspiring and fun place to work. All together we are 60 employees covering the production of API across our sites in Hillerød, Kalundborg and Gentofte. You will be part of the team with 16 colleagues based in Gentofte.
We can offer an exciting and challenging position, where you become part of a highly skilled team that acts as sparring partners and problem solvers within quality assurance issues for the production. 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 For further information, you are welcome to contact Susan Aagaard, QA Associate Manager +45 30752712 Deadline
May 15, 2023 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 look forward to reading your application, and 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 Gentofte.
Jobbet er oprettet på vores service den 20.4.2023, 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
- Gentofte
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Statistik over udbudte øvrige over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 2. maj 2024 | 28 |
| 1. maj 2024 | 33 |
| 30. april 2024 | 33 |
| 29. april 2024 | 34 |
| 28. april 2024 | 36 |
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| 20. april 2024 | 38 |
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| 17. april 2024 | 30 |
| 16. april 2024 | 29 |
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| 12. april 2024 | 31 |
| 11. april 2024 | 28 |
| 10. april 2024 | 31 |
| 9. april 2024 | 26 |
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| 7. april 2024 | 37 |
| 6. april 2024 | 37 |
| 5. april 2024 | 35 |
| 4. april 2024 | 32 |
| 3. april 2024 | 29 |
| 2. april 2024 | 29 |