Quality Engineer
- Quality
- Denmark - Hillerød
Job Description
Are you ready to make a difference and proactively influence the future device development projects in Novo Nordisk? As QA Engineer in Device Manufacturing Development (DMD) you will use your quality-focused mindset to make a serious difference and contribute to defeating diabetes worldwide.
About the department
You will be part of a team of 12 dedicated colleagues, including 10 QA Engineers, in Hillerød. Together, we are responsible for ensuring quality in realization of the devices developed by our R&D departments, processes to pilot production and transfer processes into high volume production that takes the finished product to markets worldwide.
The working relations are informal and the team values professional sparring and good humour highly.
The job
You will be Quality responsible for a number of components to Novo Nordisk Medical Devices.
As QA professional, you will prepare and maintain the quality component specifications, ensure that the quality of the components are according to the specified criteria’s. You will also be QA reviewer on change requests and non-conformities related to the components.
In your daily work, you will interact with several departments internally and externally and your success will depend on your ability to be a role model with regards to collaboration and communication with all types of colleagues and business partners.
The position offers you a unique opportunity to leave your mark on the department while realising your goals and seeing the benefits of your work.
When you start you will undergo an individual and intense training program.
You can expect travel activity related to visits to our suppliers in Europe and Asia between 20–50 days per year.
Qualifications
First and foremost you have an excellent quality mindset, good communicational skills and you can place the importance of compliance on the agenda in a positive and constructive way.
You hold an academic degree. Preferable your academic background is topped with experience from the pharmaceutical industry. However we would also like to hear from talented newly academic graduates.
Your language skills cover proficiency in English, and it is an advantage if you have experience with production and/or quality assurance within the pharmaceutical industry. It is also an advantage if you have knowledge with the requirements ISO 13485, 21 CFR Part 820 and ISO 14971.
As a person, you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments.
You work independently and make decisions regarding quality tasks and ensure the right balance between quality demands, authority demands and business needs. At the same time, you perform well in a team-oriented environment.
In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please contact Malene Fugl Andersen at + 45 3075 8982.
Deadline
19 September 2013.
- Quality
- Denmark - Hillerød
Job Description
Are you ready to make a difference and proactively influence the future device development projects in Novo Nordisk? As QA Engineer in Device Manufacturing Development (DMD) you will use your quality-focused mindset to make a serious difference and contribute to defeating diabetes worldwide.
About the department
You will be part of a team of 12 dedicated colleagues, including 10 QA Engineers, in Hillerød. Together, we are responsible for ensuring quality in realization of the devices developed by our R&D departments, processes to pilot production and transfer processes into high volume production that takes the finished product to markets worldwide.
The working relations are informal and the team values professional sparring and good humour highly.
The job
You will be Quality responsible for a number of components to Novo Nordisk Medical Devices.
As QA professional, you will prepare and maintain the quality component specifications, ensure that the quality of the components are according to the specified criteria’s. You will also be QA reviewer on change requests and non-conformities related to the components.
In your daily work, you will interact with several departments internally and externally and your success will depend on your ability to be a role model with regards to collaboration and communication with all types of colleagues and business partners.
The position offers you a unique opportunity to leave your mark on the department while realising your goals and seeing the benefits of your work.
When you start you will undergo an individual and intense training program.
You can expect travel activity related to visits to our suppliers in Europe and Asia between 20–50 days per year.
Qualifications
First and foremost you have an excellent quality mindset, good communicational skills and you can place the importance of compliance on the agenda in a positive and constructive way.
You hold an academic degree. Preferable your academic background is topped with experience from the pharmaceutical industry. However we would also like to hear from talented newly academic graduates.
Your language skills cover proficiency in English, and it is an advantage if you have experience with production and/or quality assurance within the pharmaceutical industry. It is also an advantage if you have knowledge with the requirements ISO 13485, 21 CFR Part 820 and ISO 14971.
As a person, you are known for a high commitment to finding constructive solutions as well as taking responsibility for your assignments.
You work independently and make decisions regarding quality tasks and ensure the right balance between quality demands, authority demands and business needs. At the same time, you perform well in a team-oriented environment.
In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please contact Malene Fugl Andersen at + 45 3075 8982.
Deadline
19 September 2013.