QA Professional for Qualification in Aseptic Production
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Bagsværd
At Injectable Finished Products (IFP) QA Bagsværd we are responsible for quality assurance of the aseptic production in Bagsværd. It is our responsibility to ensure that the documentation meets the regulatory GMP requirements. IFP QA Bagsværd consists of 50 dedicated and engaged employees who are divided into four different teams – Operations, AP release, QA release and Project Qualification team.
We are looking for a new colleague to join our highly engaged Project Qualification Team with direct involvement in both investment and optimisation projects at Site Bagsværd.
The job
In this role your main responsibilities will be:
• Review and approve validation processes, as well as qualification of facilities, equipment and automation systems is documented according to current GMP requirements.
• Review and approve of deviations, change requests and SOPs.
• Perform QA presence – task to be physically present on the production area to observe and help solve potential issues in real time.
• Participate in problem solving alongside our colleagues in the production, as we are present in the production every day to secure QA oversight.
As new employee you will be trained to quickly become part of the daily tasks. In the QA professional role, you will have broad contact with production in setting quality directions. This demands strong interpersonal skills and solution-oriented approach when collaborating with colleagues both in the production and QA through open and honest dialogue.
In this job you will get the opportunity to make an impact for our patients as we release products to the marketed for benefit for our patients.
Qualifications
• An academic degree within Ms. Pharmacy, veterinarian, biochemistry or similar.
• Experience within QA or other relevant GMP related job like GMP coordinator.
• Knowledge within GMP and regulations.
• The ability to make decisions based on your GMP knowledge and experience.
• Fluency in written and spoken English is a must. Danish is an advantage.
On a personal level, you are open and honest, able to engage in building relations to collaborate across departments. You have a positive attitude and are ambitious and ready to be part of our on-going effort to improve our high standards.
Working at Novo Nordisk
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.
Contact
For further information, contact Thinnakone Arounsack-Jørgensen on +45 3079 6154.
Deadline
January 16th 2023.
Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate has been identified.
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.
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We are looking for a new colleague to join our highly engaged Project Qualification Team with direct involvement in both investment and optimisation projects at Site Bagsværd.
The job
In this role your main responsibilities will be:
• Review and approve validation processes, as well as qualification of facilities, equipment and automation systems is documented according to current GMP requirements.
• Review and approve of deviations, change requests and SOPs.
• Perform QA presence – task to be physically present on the production area to observe and help solve potential issues in real time.
• Participate in problem solving alongside our colleagues in the production, as we are present in the production every day to secure QA oversight.
As new employee you will be trained to quickly become part of the daily tasks. In the QA professional role, you will have broad contact with production in setting quality directions. This demands strong interpersonal skills and solution-oriented approach when collaborating with colleagues both in the production and QA through open and honest dialogue.
In this job you will get the opportunity to make an impact for our patients as we release products to the marketed for benefit for our patients.
Qualifications
• An academic degree within Ms. Pharmacy, veterinarian, biochemistry or similar.
• Experience within QA or other relevant GMP related job like GMP coordinator.
• Knowledge within GMP and regulations.
• The ability to make decisions based on your GMP knowledge and experience.
• Fluency in written and spoken English is a must. Danish is an advantage.
On a personal level, you are open and honest, able to engage in building relations to collaborate across departments. You have a positive attitude and are ambitious and ready to be part of our on-going effort to improve our high standards.
Working at Novo Nordisk
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.
Contact
For further information, contact Thinnakone Arounsack-Jørgensen on +45 3079 6154.
Deadline
January 16th 2023.
Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate has been identified.
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.
Print job Send to e-mail
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 20.12.2022, 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
- Bagsværd
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| Dato | Alle jobs som øvrige |
|---|---|
| 26. november 2024 | 71 |
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| 27. oktober 2024 | 53 |