QA Director
Learn more about the largest site in Novo Nordisk�s global production network using this link www.novonordisk.com/kalundborg-careers
- Management
- Denmark - Kalundborg
Would you like to lead and be part of a professional and highly engaged Quality Management Team and be responsible for assuring the quality from A to Z in our production?
We are expanding our activities at our production sites in Kalundborg and are looking for a talented and ambitious director to lead the quality assurance management team, setting the standard going forward.
About the department
The QA unit is responsible for assuring quality and compliance of all production of insulin products in Denmark. This includes facilities, aseptic filling, inspection, assembly and packaging of insulin products.
The department is responsible for assuring quality and compliance for all production operation activities at Kalundborg which include aseptic production of insulin vials, assembly and packaging of insulin finished products.
Our key objectives are to assure product quality and regulatory compliance by defining quality requirements, perform quality oversight and by approving quality documents such as procedures, change request and batch- & validation documents. We participate in all production related activities to monitor the processes and to secure a strong stakeholder relation.
The job
As QA Director in Kalundborg you will join a group of 13 engaged managers and more than 100 highly skilled and competent colleagues; all dedicated to quality mind-set and continuous improvement.
You will be reporting to the Quality Vice President and have three Associate Managers with app. 30 employees. The primary responsibility will be to assure the quality of all aspects of insulin finished product production in Kalundborg incl. aseptic operation. It is expected that you actively work with development of individual and show the way going forward by creating an engaging working environment throughout the organisation. You will support the teams in decision making and take active part in internal audit and inspection from the authorities. As Quality Director you will be involved in cross functional projects and alignment activities across DFP Sites.
The job offers you an opportunity to develop both professionally and personally in a changing and inspiring environment. In order to set the bar, it is a prerequisite that you are able to handle high complexity and ensure business deliverable without compromising compliance or quality.
Qualifications<
You hold a master degree and have 6-8 years of leadership experience in the pharmaceutical industry within quality or production. You have a deep knowledge of quality assurance, master stakeholder management and collaboration and are excellent in communicating your expectations. In addition, it is expected that you have experience in ensuring compliance with standards and strive for high level of product quality through continuous improvement. You have integrity and an excellent quality mind-set. A high level of personnel decision making and authority within the team’s field of responsibility is needed. Your language skills cover proficiency in both Danish and English.
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.”
Your application and CV is welcome in Danish or English.
Contact
For further information, please contact Morten Juul Sørensen at +45 3075 1652.
Deadline
31 December 2013.
Learn more about the largest site in Novo Nordisk�s global production network using this link www.novonordisk.com/kalundborg-careers
- Management
- Denmark - Kalundborg
Would you like to lead and be part of a professional and highly engaged Quality Management Team and be responsible for assuring the quality from A to Z in our production?
We are expanding our activities at our production sites in Kalundborg and are looking for a talented and ambitious director to lead the quality assurance management team, setting the standard going forward.
About the department
The QA unit is responsible for assuring quality and compliance of all production of insulin products in Denmark. This includes facilities, aseptic filling, inspection, assembly and packaging of insulin products.
The department is responsible for assuring quality and compliance for all production operation activities at Kalundborg which include aseptic production of insulin vials, assembly and packaging of insulin finished products.
Our key objectives are to assure product quality and regulatory compliance by defining quality requirements, perform quality oversight and by approving quality documents such as procedures, change request and batch- & validation documents. We participate in all production related activities to monitor the processes and to secure a strong stakeholder relation.
The job
As QA Director in Kalundborg you will join a group of 13 engaged managers and more than 100 highly skilled and competent colleagues; all dedicated to quality mind-set and continuous improvement.
You will be reporting to the Quality Vice President and have three Associate Managers with app. 30 employees. The primary responsibility will be to assure the quality of all aspects of insulin finished product production in Kalundborg incl. aseptic operation. It is expected that you actively work with development of individual and show the way going forward by creating an engaging working environment throughout the organisation. You will support the teams in decision making and take active part in internal audit and inspection from the authorities. As Quality Director you will be involved in cross functional projects and alignment activities across DFP Sites.
The job offers you an opportunity to develop both professionally and personally in a changing and inspiring environment. In order to set the bar, it is a prerequisite that you are able to handle high complexity and ensure business deliverable without compromising compliance or quality.
Qualifications<
You hold a master degree and have 6-8 years of leadership experience in the pharmaceutical industry within quality or production. You have a deep knowledge of quality assurance, master stakeholder management and collaboration and are excellent in communicating your expectations. In addition, it is expected that you have experience in ensuring compliance with standards and strive for high level of product quality through continuous improvement. You have integrity and an excellent quality mind-set. A high level of personnel decision making and authority within the team’s field of responsibility is needed. Your language skills cover proficiency in both Danish and English.
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.”
Your application and CV is welcome in Danish or English.
Contact
For further information, please contact Morten Juul Sørensen at +45 3075 1652.
Deadline
31 December 2013.