Process Engineer
- Production
- 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 organization 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 maturing 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 of 9 engaged employees. Together we assure quality and compliance in the production of NovoPen® Echo, NovoPen® 5 and execution of new projects.
The job
You will be responsible for continuously improving our manufacturing processes in our moulding, assembly and packaging 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 working in a culture of lean thinking and with a high quality mind-set and your technical understanding you will help to optimize our processes. Finally, you will be responsible for qualifying equipment and write GMP documentation. This job will give you the opportunity to join a project organisation where co-operation and flexibility have high priority. You can look forward to a job with ever-changing assignments and a frequent rescheduling of priorities, and as such you will need to take many independent decisions within your area.
Qualifications
You hold a relevant degree in engineering (B.Sc. or M.Sc. level) within, Mechanics, Manufacturing or Medicine and Technology. You are able to drive processes proactively in a complex production environment with many stakeholders. You have knowledge and experience within documentation of quality and compliance in relation to GMP. Your area of interest is within automated processes (PLC, Robot assembly equipment etc.) both on a technical and a theoretical level.
On a personal level, you are known for dedicating yourself to work proactively in order to solve the tasks 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 in unfolding your high level of energy and spirit in an international, dynamic environment. You are fluent in spoken and written English and Danish
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.
Please mark your application "18719BR Process engineer".
Contact
For further information, please contact Thomas Bach Nielsen at +45 3075 0052.
Deadline
17 December 2013.
- Production
- 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 organization 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 maturing 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 of 9 engaged employees. Together we assure quality and compliance in the production of NovoPen® Echo, NovoPen® 5 and execution of new projects.
The job
You will be responsible for continuously improving our manufacturing processes in our moulding, assembly and packaging 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 working in a culture of lean thinking and with a high quality mind-set and your technical understanding you will help to optimize our processes. Finally, you will be responsible for qualifying equipment and write GMP documentation. This job will give you the opportunity to join a project organisation where co-operation and flexibility have high priority. You can look forward to a job with ever-changing assignments and a frequent rescheduling of priorities, and as such you will need to take many independent decisions within your area.
Qualifications
You hold a relevant degree in engineering (B.Sc. or M.Sc. level) within, Mechanics, Manufacturing or Medicine and Technology. You are able to drive processes proactively in a complex production environment with many stakeholders. You have knowledge and experience within documentation of quality and compliance in relation to GMP. Your area of interest is within automated processes (PLC, Robot assembly equipment etc.) both on a technical and a theoretical level.
On a personal level, you are known for dedicating yourself to work proactively in order to solve the tasks 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 in unfolding your high level of energy and spirit in an international, dynamic environment. You are fluent in spoken and written English and Danish
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.
Please mark your application "18719BR Process engineer".
Contact
For further information, please contact Thomas Bach Nielsen at +45 3075 0052.
Deadline
17 December 2013.