Process Support & Quality Engineer
- Quality
- Denmark - Hillerød
Are you ready to use your expertise in securing high quality work within the medical device area of Novo Nordisk?
Device Manufacturing Development (DMD) is a project organisation comprising nearly 250 engaged employees that strive to make us the best manufacturing development partner of medical devices. Our dedication is to build superior quality into device products. Our challenge is to execute an increasing portfolio of diverse development projects and bring them fast to market.
About the department
Pilot Operations handle all operational activities through the whole supply chain from purchasing of materials to delivery of finished products to our affiliates. Our main task is to support new product introduction by mature the manufacturing process of new high quality devices.
A job is waiting for you in a challenging and developing environment. In our Process support team in Hillerød you will join a team with 8 engaged employees. Together we assure quality and compliance in the production of Novo Pen Echo®, NovoPen5® and new projects. The working relations are informal and the team value professional sparring and good humour highly.
The job
As quality engineer you are responsible for maintaining the quality system in our moulding and assembly area.
Together with colleagues inside and outside the department you will be responsible for developing the quality and compliance level with high focus on corrective and preventive actions. You will be anchor person in investigations of root causes to none conformities and costumer complaints, using methodically problems solving and are always looking for improvement possibilities and for ways to optimize our processes. You enjoy working in a culture of lean thinking with a high quality mind-set. Finally, you will help qualify the equipment and write GMP documents. This job will give you the opportunity to join a project organisation where cooperation and flexibility have a high priority. You can look forward to a job with ever-changing assignments and a constant rescheduling of priorities, and as such you will need to take many independent decisions within your area. Moreover, you are supposed to participate proactively in the development of the department.
Qualifications
your approach to this position is a relevant engineering degree (B.Sc. or M.Sc. level) within Electronics, Mechanics, Manufacturing or Medicine and Technology. You have knowledge with the requirements ISO 13485, 21 CFR Part 820 and ISO 14971. You have worked with projects, and you know how to fulfil the regulatory and quality requirement.
On a personal level, you are known for dedicating yourself to working proactively to solve the task at hand. Using your ability to think outside the box, you are still able to come up with solutions or suggestions that comply with quality requirements. In addition, you are able to handle complex tasks and deliver in due time to meet our customers’ expectations. You are a team player and a skilled communicator, and you thrive on unfolding your high level of energy and spirit in an international, dynamic environment. You have a good sense of humour, and you speak and write Danish and English.
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.
Feel free to submit your job application in English.
Contact
For further information, please contact Steen Petersen at +45 3075 8987.
Deadline
5 September 2013.
- Quality
- Denmark - Hillerød
Are you ready to use your expertise in securing high quality work within the medical device area of Novo Nordisk?
Device Manufacturing Development (DMD) is a project organisation comprising nearly 250 engaged employees that strive to make us the best manufacturing development partner of medical devices. Our dedication is to build superior quality into device products. Our challenge is to execute an increasing portfolio of diverse development projects and bring them fast to market.
About the department
Pilot Operations handle all operational activities through the whole supply chain from purchasing of materials to delivery of finished products to our affiliates. Our main task is to support new product introduction by mature the manufacturing process of new high quality devices.
A job is waiting for you in a challenging and developing environment. In our Process support team in Hillerød you will join a team with 8 engaged employees. Together we assure quality and compliance in the production of Novo Pen Echo®, NovoPen5® and new projects. The working relations are informal and the team value professional sparring and good humour highly.
The job
As quality engineer you are responsible for maintaining the quality system in our moulding and assembly area.
Together with colleagues inside and outside the department you will be responsible for developing the quality and compliance level with high focus on corrective and preventive actions. You will be anchor person in investigations of root causes to none conformities and costumer complaints, using methodically problems solving and are always looking for improvement possibilities and for ways to optimize our processes. You enjoy working in a culture of lean thinking with a high quality mind-set. Finally, you will help qualify the equipment and write GMP documents. This job will give you the opportunity to join a project organisation where cooperation and flexibility have a high priority. You can look forward to a job with ever-changing assignments and a constant rescheduling of priorities, and as such you will need to take many independent decisions within your area. Moreover, you are supposed to participate proactively in the development of the department.
Qualifications
your approach to this position is a relevant engineering degree (B.Sc. or M.Sc. level) within Electronics, Mechanics, Manufacturing or Medicine and Technology. You have knowledge with the requirements ISO 13485, 21 CFR Part 820 and ISO 14971. You have worked with projects, and you know how to fulfil the regulatory and quality requirement.
On a personal level, you are known for dedicating yourself to working proactively to solve the task at hand. Using your ability to think outside the box, you are still able to come up with solutions or suggestions that comply with quality requirements. In addition, you are able to handle complex tasks and deliver in due time to meet our customers’ expectations. You are a team player and a skilled communicator, and you thrive on unfolding your high level of energy and spirit in an international, dynamic environment. You have a good sense of humour, and you speak and write Danish and English.
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.
Feel free to submit your job application in English.
Contact
For further information, please contact Steen Petersen at +45 3075 8987.
Deadline
5 September 2013.