Quality Consultant
- Research & Development
- Denmark - Hillerød
Can you enhance the understanding of our Quality Management System across an R&D organisation counting 300 employees? If so, this is your opportunity to become our new consultant and advisor. You will get the chance to take on a leading role in Device R&D and put your mark on processes and our way of working in an organisation where all our actions need to be world-class.
About the department
You will join a dedicated team of 5 LEAN & Quality Experts, located in Hillerød. We are responsible for cross-functional process improvements in Device R&D. Our focus is LEAN leadership, project planning, project risk management and QMS. Device R&D designs and develops delivery systems that enable people with chronic conditions to live their lives as they wish to. We are world leading within development of diabetes injection devices.
The job
Your overall objective is to strengthen our strategic focus within QMS, and as our new expert within this field you can look forward to having full support from the management team. A vital part of your success will depend on your ability to enhance the understanding of QMS across the Device R&D organisation’s app. 300 employees – and your ability to find easy-to-understand-and-work-with solutions in close collaboration with a great variety of managers and other stakeholders in Novo Nordisk.
You will be responsible for projects related to improvements of QMS as well as the implementation and maintenance of these. This could be e.g. projects on compliance and inspection readiness or updating of instructions and/or templates for deliverables within product development. You must challenge and align the quality improvement activities anchored in our quality activity plans. You are also responsible for coordinating Device R&D input to procedures and instructions, and you will represent Device R&D in Novo Nordisk QMS groups.
Qualifications
You have an MSc in Engineering and a minimum of 3 years’ relevant experience working with quality and change management processes within a pharmaceutical and/or medical technical company or in a consulting group. Therefore you have a sound understanding of our basic workflow and processes, and you have the overview and structured mind-set it takes to challenge and improve these. Using your positive and outgoing personality and your stamina you can take personal responsibility for your tasks and turn these into successes. To you, major challenges only make the job more fun, and you will need all of your strong communication and interpersonal skills to meet these challenges.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please call Lotte Juul Foghsgaard on +45 3075 6518.
Deadline
3 June 2013.
- Research & Development
- Denmark - Hillerød
Can you enhance the understanding of our Quality Management System across an R&D organisation counting 300 employees? If so, this is your opportunity to become our new consultant and advisor. You will get the chance to take on a leading role in Device R&D and put your mark on processes and our way of working in an organisation where all our actions need to be world-class.
About the department
You will join a dedicated team of 5 LEAN & Quality Experts, located in Hillerød. We are responsible for cross-functional process improvements in Device R&D. Our focus is LEAN leadership, project planning, project risk management and QMS. Device R&D designs and develops delivery systems that enable people with chronic conditions to live their lives as they wish to. We are world leading within development of diabetes injection devices.
The job
Your overall objective is to strengthen our strategic focus within QMS, and as our new expert within this field you can look forward to having full support from the management team. A vital part of your success will depend on your ability to enhance the understanding of QMS across the Device R&D organisation’s app. 300 employees – and your ability to find easy-to-understand-and-work-with solutions in close collaboration with a great variety of managers and other stakeholders in Novo Nordisk.
You will be responsible for projects related to improvements of QMS as well as the implementation and maintenance of these. This could be e.g. projects on compliance and inspection readiness or updating of instructions and/or templates for deliverables within product development. You must challenge and align the quality improvement activities anchored in our quality activity plans. You are also responsible for coordinating Device R&D input to procedures and instructions, and you will represent Device R&D in Novo Nordisk QMS groups.
Qualifications
You have an MSc in Engineering and a minimum of 3 years’ relevant experience working with quality and change management processes within a pharmaceutical and/or medical technical company or in a consulting group. Therefore you have a sound understanding of our basic workflow and processes, and you have the overview and structured mind-set it takes to challenge and improve these. Using your positive and outgoing personality and your stamina you can take personal responsibility for your tasks and turn these into successes. To you, major challenges only make the job more fun, and you will need all of your strong communication and interpersonal skills to meet these challenges.
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.
Contact
For further information, please call Lotte Juul Foghsgaard on +45 3075 6518.
Deadline
3 June 2013.