GMP partner
- Production
- Denmark - Bagsværd
Are you ready to take the next step in your career, you now have the opportunity. You will be a key player in ensuring quality and compliance for a specific business area consisting of a number of departments. You will be a member of the local Management team and primary sparring partner for the Vice President and Managers on GMP issues.
About the department
We are looking for GMP Partners to our sites in Bagsværd and Hillerød. In Bagsværd we focus on aseptic production and in Hillerød primarily on medical devices. The GMP Partner and GMP Coordinator setup is a matrix organisation, where you will head the GMP Coordinators across different departments as their Professional Manager. The number of GMP Coordinators varies depending on the size of the business area.
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 Quality Management Review (QMR), and you play an active role in audits and inspections, having the GMP Coordinators as your skilled co-workers. 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 Lene Uhre Hansen at +45 3079 9308.
Learn more about Novo Nordisk Product Supply and working in QA using this link www.novonordisk.com/careers/QA
Deadline
6 September 2013.
- Production
- Denmark - Bagsværd
Are you ready to take the next step in your career, you now have the opportunity. You will be a key player in ensuring quality and compliance for a specific business area consisting of a number of departments. You will be a member of the local Management team and primary sparring partner for the Vice President and Managers on GMP issues.
About the department
We are looking for GMP Partners to our sites in Bagsværd and Hillerød. In Bagsværd we focus on aseptic production and in Hillerød primarily on medical devices. The GMP Partner and GMP Coordinator setup is a matrix organisation, where you will head the GMP Coordinators across different departments as their Professional Manager. The number of GMP Coordinators varies depending on the size of the business area.
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 Quality Management Review (QMR), and you play an active role in audits and inspections, having the GMP Coordinators as your skilled co-workers. 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 Lene Uhre Hansen at +45 3079 9308.
Learn more about Novo Nordisk Product Supply and working in QA using this link www.novonordisk.com/careers/QA
Deadline
6 September 2013.