QA Chemist - Temp.
- Quality
- Denmark - Bagsværd
Do you want a key role in ensuring the quality of the insulin products and compliance with regulatory requirements? If so, then seize the opportunity and join QA of the aseptic production (AP) in Site Denmark.
About the department
In QA AP we are responsible of assuring quality and compliance in the aseptic production of insulin products in Site Denmark. It is our responsibility that the documentation related to the aseptic production is in compliance with regulatory requirements and the Novo Nordisk quality management system.
In QA AP you will join a department of 46 highly motivated and dedicated employees which is divided in three teams - two teams in Bagsværd and one team in Hillerød. In a close collaboration with the production we ensure a high level of quality and play a key role in releasing insulin products to diabetics all over the world.
We are at the moment looking for a QA chemist (maternity temp, 12 month) to our chemist- and principal scientist team in Bagsværd.
The Job
As a QA chemist you will be a decisive factor in making sure that the released products lives up the current GMP and regulatory requirements. You will be involved in the handling of incidents in the production and participate in systematic problem solving together with process support and production. Likewise, you will perform different tasks related to quality assurance, e.g. approval of batch documentation and production related documents. We operate in a LEAN environment where we focus on optimising our processes. You will therefore be involved in the implementation of new initiative which can optimise our daily work.
Qualifications
You hold an academic degree and preferable your academic background is topped with work experience from the pharmaceutical industry. On a personal level you are known for you positive mindset, flexibility and persistence. You have a strong quality mindset, meet your deadlines, and know how to prioritise between different tasks in a dynamic environment. You like and are good at coordinating different tasks for both yourself and other people and you demonstrate an ability to find the right solutions with your colleagues. Your language skills cover proficiency in both Danish and English.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Henriette Kyed, +45 3075 2194.
Learn more about Novo Nordisk Product Supply and working in QA using this link www.novonordisk.com/careers/QA.
Deadline
29 September 2013
- Quality
- Denmark - Bagsværd
Do you want a key role in ensuring the quality of the insulin products and compliance with regulatory requirements? If so, then seize the opportunity and join QA of the aseptic production (AP) in Site Denmark.
About the department
In QA AP we are responsible of assuring quality and compliance in the aseptic production of insulin products in Site Denmark. It is our responsibility that the documentation related to the aseptic production is in compliance with regulatory requirements and the Novo Nordisk quality management system.
In QA AP you will join a department of 46 highly motivated and dedicated employees which is divided in three teams - two teams in Bagsværd and one team in Hillerød. In a close collaboration with the production we ensure a high level of quality and play a key role in releasing insulin products to diabetics all over the world.
We are at the moment looking for a QA chemist (maternity temp, 12 month) to our chemist- and principal scientist team in Bagsværd.
The Job
As a QA chemist you will be a decisive factor in making sure that the released products lives up the current GMP and regulatory requirements. You will be involved in the handling of incidents in the production and participate in systematic problem solving together with process support and production. Likewise, you will perform different tasks related to quality assurance, e.g. approval of batch documentation and production related documents. We operate in a LEAN environment where we focus on optimising our processes. You will therefore be involved in the implementation of new initiative which can optimise our daily work.
Qualifications
You hold an academic degree and preferable your academic background is topped with work experience from the pharmaceutical industry. On a personal level you are known for you positive mindset, flexibility and persistence. You have a strong quality mindset, meet your deadlines, and know how to prioritise between different tasks in a dynamic environment. You like and are good at coordinating different tasks for both yourself and other people and you demonstrate an ability to find the right solutions with your colleagues. Your language skills cover proficiency in both Danish and English.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please contact Henriette Kyed, +45 3075 2194.
Learn more about Novo Nordisk Product Supply and working in QA using this link www.novonordisk.com/careers/QA.
Deadline
29 September 2013