Senior Quality Coordinator and Test Engineer
- Quality, senior position
- Denmark - Hillerød
In this job, 366 million people worldwide depend on you to improve verification processes and documentation in the development of the world’s best medical devices. If you find challenges like this exciting and inspiring, you may be our new Quality Coordinator and Test Engineer within verification of medical devices.
About the department
Device Testing and Coordination is part of the Competency Centre in the Device Research and Development unit. We are 21 dedicated laboratory technicians and engineers, ensuring the functional and environmental testing and verification of medical device prototypes. Currently the department is facing new challenges and responsibilities within design verification. This means that our existing quality setup needs to be evaluated and new projects need to be driven in our test department.
The job
The job consists of two roles. As a Quality Coordinator you will, in close collaboration with quality assurance colleagues in other units, ensure that we reach the agreed level of quality in our department. You will be responsible for our process with regard to quality and quality related tasks that need to be aligned with our quality assurance department, and afterwards implemented our the department. You will also be responsible for the process of making our documentation meet relevant medical device quality standards and regulatory requirements from our key markets. As a Test Engineer you will participate in the development of test methods and test documentation together with the team of test engineers. Furthermore you will act as a sparring partner for our test engineers when it comes to test and verification documentation.
Qualifications
You hold an academic degree in mechanical engineering or equivalent. You have significant experience with quality assurance and design verification, preferably within medical device development or manufacturing. Experience with ISO 13485 and FDA 21 CFR, part 820 in laboratories is very relevant. We expect you to be able to work independently and actively seek support from your quality assurance colleagues when needed. You must be able to work with frequently changing priorities and find it easy to switch between your two roles. You make a difference, and due to your dedicated and determined approach you are able to complete your tasks in close cooperation with your colleagues. You work in a structured way and are used to deliver according to targets. You are fluent in both written and spoken English on a professional level.
At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.
Contact
For further information, please contact Torben Jørgensen Herslund at +45 3079 0956 or Katrine Hammer at +45 3079 2038.
Deadline
17 August 2013.
- Quality, senior position
- Denmark - Hillerød
In this job, 366 million people worldwide depend on you to improve verification processes and documentation in the development of the world’s best medical devices. If you find challenges like this exciting and inspiring, you may be our new Quality Coordinator and Test Engineer within verification of medical devices.
About the department
Device Testing and Coordination is part of the Competency Centre in the Device Research and Development unit. We are 21 dedicated laboratory technicians and engineers, ensuring the functional and environmental testing and verification of medical device prototypes. Currently the department is facing new challenges and responsibilities within design verification. This means that our existing quality setup needs to be evaluated and new projects need to be driven in our test department.
The job
The job consists of two roles. As a Quality Coordinator you will, in close collaboration with quality assurance colleagues in other units, ensure that we reach the agreed level of quality in our department. You will be responsible for our process with regard to quality and quality related tasks that need to be aligned with our quality assurance department, and afterwards implemented our the department. You will also be responsible for the process of making our documentation meet relevant medical device quality standards and regulatory requirements from our key markets. As a Test Engineer you will participate in the development of test methods and test documentation together with the team of test engineers. Furthermore you will act as a sparring partner for our test engineers when it comes to test and verification documentation.
Qualifications
You hold an academic degree in mechanical engineering or equivalent. You have significant experience with quality assurance and design verification, preferably within medical device development or manufacturing. Experience with ISO 13485 and FDA 21 CFR, part 820 in laboratories is very relevant. We expect you to be able to work independently and actively seek support from your quality assurance colleagues when needed. You must be able to work with frequently changing priorities and find it easy to switch between your two roles. You make a difference, and due to your dedicated and determined approach you are able to complete your tasks in close cooperation with your colleagues. You work in a structured way and are used to deliver according to targets. You are fluent in both written and spoken English on a professional level.
At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.
Contact
For further information, please contact Torben Jørgensen Herslund at +45 3079 0956 or Katrine Hammer at +45 3079 2038.
Deadline
17 August 2013.