Advanced QA
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Værløse
Are you ready to play a crucial role in ensuring the quality and safety of our products for patients worldwide? Do you thrive in a challenging and ever-changing environment? Would you like to help us on our journey of an exciting transition towards modern technology with many ongoing projects providing opportunities for impacting future production and capacity expansions as well as personal development?
If your response to this questions is yes, then you may be our new colleague in Biotech and Rare Disease QA, located in Værløse (assembly and packaging) and Gentofte (packaging) as well as the project office located in Høje Taastrup. Apply today and join us for a life changing career!
The position
As a Quality Assurance (QA) Professional you are the gatekeeper for GMP compliance. You will join the team as a Quality Assurance Professional with experience in validation and GMP, and a strong quality mindset to ensure highest quality products for our patients.
Your key responsibilities will include:
• reviewing and approving documentation relating to both new and existing equipment
• perform Quality Assurance oversight of already existing and new equipment
• review and approve production related documentation
• having a close, good communication and collaboration with our production and stakeholders
• performing Quality Assurance oversight by being present in our production facilities.
As part of the Quality Assurance team, you will have the opportunity to work with highly skilled people and get a solid understanding of GMP and manufacturing processes in a packaging department. The work environment we foster is informal, and the team is characterized by a high-quality mindset and a cooperative spirit.
Qualifications
To be a competitive candidate, you should have:
• a master’s degree in Pharmacy, Chemistry, Engineering or similar
• + 2 yrs. GMP experience from the pharmaceutical industry
• a level of IT flair and knowledge of digitalization tools is an advantage
• Professional proficiency in Danish and English
On a personal level, you demonstrate great communication and collaboration skills. Your drivers are a great personal commitment and accountability in every aspect of your work. The key to succeed in this role is to have a high-quality mindset and a respect towards deadlines.
About the department
We are a diverse department with 29 employees divided into two areas within Biotech and Rare Disease QA. We are responsible for the quality assurance of our pharmaceutical products of assembled and finished packed products. You will become part of a dedicated team of academics in a casual atmosphere and where we take good care of each other. The team covers two separate packaging departments located in Værløse (assembly and packaging) and Gentofte (packaging).
Our department is in an exciting transition towards modern technology with many ongoing projects providing opportunities for impacting future production and personal development.
Working at Novo Nordisk
Novo Nordisk 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 61,000 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 Novo Nordisk, 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 Associate Manager Benedicte Hvidberg at +45 3079 2145.
Deadline
March 10th 2024. Please note that applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates have been identified.
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 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.
If your response to this questions is yes, then you may be our new colleague in Biotech and Rare Disease QA, located in Værløse (assembly and packaging) and Gentofte (packaging) as well as the project office located in Høje Taastrup. Apply today and join us for a life changing career!
The position
As a Quality Assurance (QA) Professional you are the gatekeeper for GMP compliance. You will join the team as a Quality Assurance Professional with experience in validation and GMP, and a strong quality mindset to ensure highest quality products for our patients.
Your key responsibilities will include:
• reviewing and approving documentation relating to both new and existing equipment
• perform Quality Assurance oversight of already existing and new equipment
• review and approve production related documentation
• having a close, good communication and collaboration with our production and stakeholders
• performing Quality Assurance oversight by being present in our production facilities.
As part of the Quality Assurance team, you will have the opportunity to work with highly skilled people and get a solid understanding of GMP and manufacturing processes in a packaging department. The work environment we foster is informal, and the team is characterized by a high-quality mindset and a cooperative spirit.
Qualifications
To be a competitive candidate, you should have:
• a master’s degree in Pharmacy, Chemistry, Engineering or similar
• + 2 yrs. GMP experience from the pharmaceutical industry
• a level of IT flair and knowledge of digitalization tools is an advantage
• Professional proficiency in Danish and English
On a personal level, you demonstrate great communication and collaboration skills. Your drivers are a great personal commitment and accountability in every aspect of your work. The key to succeed in this role is to have a high-quality mindset and a respect towards deadlines.
About the department
We are a diverse department with 29 employees divided into two areas within Biotech and Rare Disease QA. We are responsible for the quality assurance of our pharmaceutical products of assembled and finished packed products. You will become part of a dedicated team of academics in a casual atmosphere and where we take good care of each other. The team covers two separate packaging departments located in Værløse (assembly and packaging) and Gentofte (packaging).
Our department is in an exciting transition towards modern technology with many ongoing projects providing opportunities for impacting future production and personal development.
Working at Novo Nordisk
Novo Nordisk 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 61,000 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 Novo Nordisk, 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 Associate Manager Benedicte Hvidberg at +45 3079 2145.
Deadline
March 10th 2024. Please note that applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates have been identified.
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 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 Værløse.
Jobbet er oprettet på vores service den 8.1.2024, 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
- Værløse
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Statistik over udbudte øvrige i Værløse over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 28. juli 2024 | 7 |
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| 25. juli 2024 | 7 |
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| 1. juli 2024 | 5 |
| 30. juni 2024 | 4 |
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| 28. juni 2024 | 5 |