QA Chemist for Aseptic Production
- Quality
- Denmark - Hillerød
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) and quality control (QC) in Site Denmark.
About the Department
In QA AP/QC we are responsible of assuring quality and compliance in the AP of insulin products and QC in Site Denmark. It is our responsibility that the documentation related to AP and QC is in compliance with regulatory requirements and the Novo Nordisk quality management system.
In QA AP/QC you will join a department of 48 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 and QC 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 (permanent position) to our team in Hillerød.
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 preferably your academic background is topped with at least one year of relevant 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 Morten Petersen, +45 3075 0663.
Learn more about Novo Nordisk Product Supply and working in QA using this link www.novonordisk.com/careers/QA
Deadline
25 August 2013.
- Quality
- Denmark - Hillerød
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) and quality control (QC) in Site Denmark.
About the Department
In QA AP/QC we are responsible of assuring quality and compliance in the AP of insulin products and QC in Site Denmark. It is our responsibility that the documentation related to AP and QC is in compliance with regulatory requirements and the Novo Nordisk quality management system.
In QA AP/QC you will join a department of 48 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 and QC 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 (permanent position) to our team in Hillerød.
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 preferably your academic background is topped with at least one year of relevant 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 Morten Petersen, +45 3075 0663.
Learn more about Novo Nordisk Product Supply and working in QA using this link www.novonordisk.com/careers/QA
Deadline
25 August 2013.