Quality coordinator
- Production
- Denmark - Gentofte
Are you interested in working with our broad portfolio of products in Biopharm and help us in being Fast to market? In Biopharm Manufacturing Development we are responsible for support to our productions, transfer of new products from R&D and continuous optimizations of our many processes. You will be a key player in ensuring quality and compliance for Biopharm API Support consisting of a number of teams. You will be a member of the local Management team and primary sparring partner for the Director and Associate Managers on GMP issues.
About the department
We focus on support to Bioparm API production, product transfer from R&D and production of supporting proteins. You will have 40 highly qualified and motivated colleagues. You will be responsible for quality and refer directly to the Director for Biopharm API Support.
The job
As GMP Partner you have the overall responsibility for setting the targets on quality and compliance for your area and for making sure that they will be met. As such, you bring in the latest knowledge within GMP when you challenge our business managers to bring GMP and quality to the top of the agenda. You ensure that the area is in compliance with the authorities’ and Novo Nordisk’s regulations, including ISO9001:2008, and you will become your area’s representative in our cross-organisational GMP group/GMP board. You are also responsible for the departments input to the Quality Management Review (QMR), and you play an active role in audits and inspections. You will participate in our GMP network meetings with your peers for sparring, sharing and development of GMP and QMS related topics. The job involves contact and interaction to many different stakeholders in the organisation, from operators, maintenance, LEAN professionals, project managers, and to all line management levels.
Qualifications
You hold a degree at minimum master’s level. Your academic background is topped with experience from a pharmaceutical production company where you have gained solid experience within quality, GMP and ISO9001. You are used to create results through projects and know the importance of team collaboration. To succeed, you must thrive in a role where you take leadership, initiate and coordinate a large number of actions and projects. This requires an excellent overview, a structured mind-set and a dedicated way of working as well as very good communication skills. Working cross-organisationally, your networking skills will also be crucial as well as your ability to balance when to compromise and when to stand firm. Finally, you must master English and Danish, written and spoken.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better.
In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Casper Leuenhagen at +45 3079 4751.
Deadline
22 September 2013.
- Production
- Denmark - Gentofte
Are you interested in working with our broad portfolio of products in Biopharm and help us in being Fast to market? In Biopharm Manufacturing Development we are responsible for support to our productions, transfer of new products from R&D and continuous optimizations of our many processes. You will be a key player in ensuring quality and compliance for Biopharm API Support consisting of a number of teams. You will be a member of the local Management team and primary sparring partner for the Director and Associate Managers on GMP issues.
About the department
We focus on support to Bioparm API production, product transfer from R&D and production of supporting proteins. You will have 40 highly qualified and motivated colleagues. You will be responsible for quality and refer directly to the Director for Biopharm API Support.
The job
As GMP Partner you have the overall responsibility for setting the targets on quality and compliance for your area and for making sure that they will be met. As such, you bring in the latest knowledge within GMP when you challenge our business managers to bring GMP and quality to the top of the agenda. You ensure that the area is in compliance with the authorities’ and Novo Nordisk’s regulations, including ISO9001:2008, and you will become your area’s representative in our cross-organisational GMP group/GMP board. You are also responsible for the departments input to the Quality Management Review (QMR), and you play an active role in audits and inspections. You will participate in our GMP network meetings with your peers for sparring, sharing and development of GMP and QMS related topics. The job involves contact and interaction to many different stakeholders in the organisation, from operators, maintenance, LEAN professionals, project managers, and to all line management levels.
Qualifications
You hold a degree at minimum master’s level. Your academic background is topped with experience from a pharmaceutical production company where you have gained solid experience within quality, GMP and ISO9001. You are used to create results through projects and know the importance of team collaboration. To succeed, you must thrive in a role where you take leadership, initiate and coordinate a large number of actions and projects. This requires an excellent overview, a structured mind-set and a dedicated way of working as well as very good communication skills. Working cross-organisationally, your networking skills will also be crucial as well as your ability to balance when to compromise and when to stand firm. Finally, you must master English and Danish, written and spoken.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better.
In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Casper Leuenhagen at +45 3079 4751.
Deadline
22 September 2013.