Quality & cLEAN Coordinator (Professional)
- Production
- Denmark - Bagsværd
Do you have experience with GMP, and can you handle a great variety of tasks from identifying and driving projects over writing Standard Operating Procedures to setting and following up on goals? If you thrive on working with quality and compliance in a LEAN manner, you could be our new Quality & cLEAN coordinator.
About the department
You will join QC Packaging Materials in Bagsværd. We are responsible for quality control of printed and primary packaging materials to production departments in Denmark and abroad. Today we are 39 employees in two teams. You will be referring to the department manager and will become part of our management team. Our focus is to deliver high quality adhering to agreed deadlines and budgets every time.
The job
Your overall objective is to help us set and meet the department goals within quality and compliance, and make sure that our way of doing things represent best practice. You coordinate and are operationally responsible for quality and cLEAN projects where you
define milestones and ensure that we meet the agreed deadlines. As such, you will be in charge of different improvement projects in the department and be part of cross-organizational groups. As quality coordinator you will have an important role in ensuring high standards in compliance with regulations and procedures. You are also responsible for the departments input to the Quality Management Review (QMR), and you play an active role in audits and inspections. Following up on targets and facilitating our incidents handling are other tasks on your agenda. All in all, you can look forward to an exciting and challenging job.
Qualifications
Your background is a master’s degree most likely within the natural sciences. You have experience with quality, GMP and ISO9001, including hands-on experience with quality control. In addition, you share our interest in meeting high standards in everything we do. If you do not have practical experience with LEAN already, you are eager to learn all about it. You are known to be very structured, and you can analyze an incident and pinpoint the cause and afterwards adjust methods/procedures/processes in order to prevent the problem from recurring. As quality and cLEAN coordinator you must also thrive on having contact to many people, and you can use your good communication and interpersonal skills to make your contacts co-players on your quality agenda. To succeed, it is also vital that you can independently plan and drive your own tasks. Likewise your ability to balance when to compromise and when to stand firm will be crucial.
Finally, you must master English and Danish, written and spoken.
At Novo Nordisk, you will help millions of people who are living with diabetes. We expect high performance and the ambition to make your mark on our business. In exchange, we offer global opportunities for professional and personal development.
Contact
For further information, please contact Marie-Louise Haldbo at +45 3075 4206.
Deadline
28 September 2013.
- Production
- Denmark - Bagsværd
Do you have experience with GMP, and can you handle a great variety of tasks from identifying and driving projects over writing Standard Operating Procedures to setting and following up on goals? If you thrive on working with quality and compliance in a LEAN manner, you could be our new Quality & cLEAN coordinator.
About the department
You will join QC Packaging Materials in Bagsværd. We are responsible for quality control of printed and primary packaging materials to production departments in Denmark and abroad. Today we are 39 employees in two teams. You will be referring to the department manager and will become part of our management team. Our focus is to deliver high quality adhering to agreed deadlines and budgets every time.
The job
Your overall objective is to help us set and meet the department goals within quality and compliance, and make sure that our way of doing things represent best practice. You coordinate and are operationally responsible for quality and cLEAN projects where you
define milestones and ensure that we meet the agreed deadlines. As such, you will be in charge of different improvement projects in the department and be part of cross-organizational groups. As quality coordinator you will have an important role in ensuring high standards in compliance with regulations and procedures. You are also responsible for the departments input to the Quality Management Review (QMR), and you play an active role in audits and inspections. Following up on targets and facilitating our incidents handling are other tasks on your agenda. All in all, you can look forward to an exciting and challenging job.
Qualifications
Your background is a master’s degree most likely within the natural sciences. You have experience with quality, GMP and ISO9001, including hands-on experience with quality control. In addition, you share our interest in meeting high standards in everything we do. If you do not have practical experience with LEAN already, you are eager to learn all about it. You are known to be very structured, and you can analyze an incident and pinpoint the cause and afterwards adjust methods/procedures/processes in order to prevent the problem from recurring. As quality and cLEAN coordinator you must also thrive on having contact to many people, and you can use your good communication and interpersonal skills to make your contacts co-players on your quality agenda. To succeed, it is also vital that you can independently plan and drive your own tasks. Likewise your ability to balance when to compromise and when to stand firm will be crucial.
Finally, you must master English and Danish, written and spoken.
At Novo Nordisk, you will help millions of people who are living with diabetes. We expect high performance and the ambition to make your mark on our business. In exchange, we offer global opportunities for professional and personal development.
Contact
For further information, please contact Marie-Louise Haldbo at +45 3075 4206.
Deadline
28 September 2013.