QA Professional
- Quality
- Denmark - Hillerød
Would you like to help securing Novo Nordisk A/S portfolio of prefilled devices continuously is improved to the benefit of our customers? Do you get energised by working in a team; handle multiple tasks on a daily basis in a global environment? Then you might be the person we are looking for in Device Manufacturing Development (DMD), Prefilled QA.
About the department
DMD Prefilled QA is responsible for quality assurance activities and continuous optimization of the Novo Nordisk A/S portfolio of prefilled devices (i.e. FlexPen® and FlexTouch®).The department works with suppliers and assembly sites that are located in Denmark, Europe, USA and Brazil. Your closest colleagues are 50 highly qualified professionals within Device Manufacturing Development (9 of these in Prefilled QA) working with the support to both marketed and new products within the prefilled device area.
The Job
You will contribute to the Device Manufacturing Development organisation by representing Quality Assurance in one of the most important business areas within Novo Nordisk A/S. The most important focus areas within DMD Prefilled QA are:
Continuous improvement of the Quality Management System for prefilled devices to secure the right product quality and to support the alignment of quality ambitions across the entire supply chain. Support to processes from component level to assembly and packaging processes (risk management, quality specification etc.) including laboratory methods for final release testing. Support to costumer complaint investigation. Support to optimization projects and documentation of changes to both product and processes. Support to incident handling when requested from the Manufacturing sites. Building strong partnership with internal stakeholders within Manufacturing, Device R&D and Manufacturing Development.
Qualifications
You hold a relevant academic degree in engineering, pharmacy or equivalent and have relevant working experience ideally within combination products (drug/device). You have an up-to-date knowledge of relevant GMP requirements. We expect you to work independently, and that you actively seek support from your colleagues when needed. You are familiar working in a team and used to deliver according to targets. You make a difference, and by your dedicated and determined approach you complete your tasks in close cooperation with your colleagues. You work in a structured way and you get energised by learning new things. You are robust, can keep focus and you have good communication skills. Quality is essential to you and incorporated in your daily work. On a personal level you are ambitious and have a great interest in developing yourself. You are fluent in both written and spoken English on a professional level.
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 call Anja Stranum Monger at +45 3075 7049.
Deadline
4 October 2013.
- Quality
- Denmark - Hillerød
Would you like to help securing Novo Nordisk A/S portfolio of prefilled devices continuously is improved to the benefit of our customers? Do you get energised by working in a team; handle multiple tasks on a daily basis in a global environment? Then you might be the person we are looking for in Device Manufacturing Development (DMD), Prefilled QA.
About the department
DMD Prefilled QA is responsible for quality assurance activities and continuous optimization of the Novo Nordisk A/S portfolio of prefilled devices (i.e. FlexPen® and FlexTouch®).The department works with suppliers and assembly sites that are located in Denmark, Europe, USA and Brazil. Your closest colleagues are 50 highly qualified professionals within Device Manufacturing Development (9 of these in Prefilled QA) working with the support to both marketed and new products within the prefilled device area.
The Job
You will contribute to the Device Manufacturing Development organisation by representing Quality Assurance in one of the most important business areas within Novo Nordisk A/S. The most important focus areas within DMD Prefilled QA are:
Continuous improvement of the Quality Management System for prefilled devices to secure the right product quality and to support the alignment of quality ambitions across the entire supply chain. Support to processes from component level to assembly and packaging processes (risk management, quality specification etc.) including laboratory methods for final release testing. Support to costumer complaint investigation. Support to optimization projects and documentation of changes to both product and processes. Support to incident handling when requested from the Manufacturing sites. Building strong partnership with internal stakeholders within Manufacturing, Device R&D and Manufacturing Development.
Qualifications
You hold a relevant academic degree in engineering, pharmacy or equivalent and have relevant working experience ideally within combination products (drug/device). You have an up-to-date knowledge of relevant GMP requirements. We expect you to work independently, and that you actively seek support from your colleagues when needed. You are familiar working in a team and used to deliver according to targets. You make a difference, and by your dedicated and determined approach you complete your tasks in close cooperation with your colleagues. You work in a structured way and you get energised by learning new things. You are robust, can keep focus and you have good communication skills. Quality is essential to you and incorporated in your daily work. On a personal level you are ambitious and have a great interest in developing yourself. You are fluent in both written and spoken English on a professional level.
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 call Anja Stranum Monger at +45 3075 7049.
Deadline
4 October 2013.