Advanced QA Release Engineer
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Hjørring
Do you enjoy critical thinking, innovation and problem solving? Are you passionate about ensuring the delivery of high-quality medical products to patients? Do you thrive in a collaborative environment where teamwork is a key to success?
If so, consider becoming a vital part of Novo Nordisk's Quality Assurance (QA) department within Global Contract Manufacturing (GCM) Devices, External Batch Release in Hjørring. Read on to learn more and apply now! The Position
We are on the lookout for an Advanced QA Release Engineer with good communication skills, continuous improvement mindset and the desire to work closely together with a lot of different stakeholders. As our new colleague within batch release your main tasks will involve:
• Review documentation and release components and needle products from our suppliers and contract manufacturer.
• Working with GMP and documentation tasks.
• Having an eye for detail and a strong quality mindset to perform daily tasks. You thrive with routine tasks and maintain focus in an environment where priorities can change rapidly. The position calls for your ability to be self-driven, but at the same time understand the importance of teamwork. Qualifications
We expect our ideal candidate to have the following:
• Master’s degree in Science or other relevant field.
• A background that provides you with a solid technical understanding for QA (preferably from a GMP production environment as a QA or Process Engineer).
• 1+ yrs of experience working with GMP and documentation.
• IT knowledge or technical flair and an interest to expand your knowledge within this are. IT knowledge may include e.g. SAP, Digitalised Batch Release (DBR) and LIMS.
• Ideally, you have knowledge of requirements for production records and good documentation practise, and you have an understanding for simplicity in these processes.
• Proficiency in Danish and English, both oral and written. As a person, you are analytical, systematic and you possess excellent communication skills. You are curious, willing to learn, and good at asking questions, and you can stay engaged in a position where days look similar from time to time.
About the Department
You will be a part of the Quality department of our external needle production and have a workday with a large degree of independence. We are a team of 12 employees responsible for the Quality Assurance of all needle products produced externally by . Our main purpose is to safeguard patient safety, product quality and compliance of pen needles and components. You will find that you have rich opportunities to share ideas, create great results and develop yourself, both on a professional and on a personal level. Working at
is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at , we’re working toward something bigger than ourselves, and it’s a collective effort. Join us! Together, we go further. Together, we’re life changing. Contact
For further information, please contact Manager, Maja Høegh Christensen at +. Deadline
25 October 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 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.
If so, consider becoming a vital part of Novo Nordisk's Quality Assurance (QA) department within Global Contract Manufacturing (GCM) Devices, External Batch Release in Hjørring. Read on to learn more and apply now! The Position
We are on the lookout for an Advanced QA Release Engineer with good communication skills, continuous improvement mindset and the desire to work closely together with a lot of different stakeholders. As our new colleague within batch release your main tasks will involve:
• Review documentation and release components and needle products from our suppliers and contract manufacturer.
• Working with GMP and documentation tasks.
• Having an eye for detail and a strong quality mindset to perform daily tasks. You thrive with routine tasks and maintain focus in an environment where priorities can change rapidly. The position calls for your ability to be self-driven, but at the same time understand the importance of teamwork. Qualifications
We expect our ideal candidate to have the following:
• Master’s degree in Science or other relevant field.
• A background that provides you with a solid technical understanding for QA (preferably from a GMP production environment as a QA or Process Engineer).
• 1+ yrs of experience working with GMP and documentation.
• IT knowledge or technical flair and an interest to expand your knowledge within this are. IT knowledge may include e.g. SAP, Digitalised Batch Release (DBR) and LIMS.
• Ideally, you have knowledge of requirements for production records and good documentation practise, and you have an understanding for simplicity in these processes.
• Proficiency in Danish and English, both oral and written. As a person, you are analytical, systematic and you possess excellent communication skills. You are curious, willing to learn, and good at asking questions, and you can stay engaged in a position where days look similar from time to time.
About the Department
You will be a part of the Quality department of our external needle production and have a workday with a large degree of independence. We are a team of 12 employees responsible for the Quality Assurance of all needle products produced externally by . Our main purpose is to safeguard patient safety, product quality and compliance of pen needles and components. You will find that you have rich opportunities to share ideas, create great results and develop yourself, both on a professional and on a personal level. Working at
is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at , we’re working toward something bigger than ourselves, and it’s a collective effort. Join us! Together, we go further. Together, we’re life changing. Contact
For further information, please contact Manager, Maja Høegh Christensen at +. Deadline
25 October 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 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 Hjørring.
Jobbet er oprettet på vores service den 11.10.2024, 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
- Hjørring
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Statistik over udbudte øvrige i Hjørring over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 18. november 2024 | 10 |
| 17. november 2024 | 10 |
| 16. november 2024 | 10 |
| 15. november 2024 | 9 |
| 14. november 2024 | 9 |
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| 11. november 2024 | 8 |
| 10. november 2024 | 8 |
| 9. november 2024 | 8 |
| 8. november 2024 | 7 |
| 7. november 2024 | 7 |
| 6. november 2024 | 7 |
| 5. november 2024 | 7 |
| 4. november 2024 | 6 |
| 3. november 2024 | 6 |
| 2. november 2024 | 6 |
| 1. november 2024 | 6 |
| 31. oktober 2024 | 6 |
| 30. oktober 2024 | 5 |
| 29. oktober 2024 | 6 |
| 28. oktober 2024 | 6 |
| 27. oktober 2024 | 7 |
| 26. oktober 2024 | 7 |
| 25. oktober 2024 | 6 |
| 24. oktober 2024 | 6 |
| 23. oktober 2024 | 6 |
| 22. oktober 2024 | 6 |
| 21. oktober 2024 | 7 |
| 20. oktober 2024 | 8 |
| 19. oktober 2024 | 8 |