GMP partner
- Production
- Denmark - Hillerød
Are you ready to take the next step in your career - you now have the opportunity!!
You will be key player in ensuring quality and compliance for a large business area in Site Hillerød consisting 5 departments, more than 20 managers and app. 350 employees. You will be a key member of the ambitious, local management team and primary sparring partner for the Vice President and directors on critical GMP issues.
About the department
We are looking for GMP Partners to our sites in Hillerød 25A where we focus on both aseptic production and on medical devices. The GMP-partner and coordinator setup is a matrix organisation, where you will head up 5 GMP Coordinators across the different departments.
The job
As GMP Partner you have the overall responsibility for setting the targets on quality 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 common 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 Site Denmark’s 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 SDKs GMP network meetings with your peers for sparring, sharing and development of GMP and QMS related topics. The network is owned and facilitated by the QMS function.
The job involves contact and interaction to many different stakeholders in the organisation, from operators, maintenance, cLEAN professionals, project managers and to all line management levels. Your role calls for strong change management and communication skills and ability to create the right quality and compliance mindset.
Qualifications
You hold a degree at minimum master’s level. Your academic background is topped with experience from a pharmaceutical production where you have gained solid experience within quality, GMP and ISO9001. Maybe you already work in Novo Nordisk as a manager, project manager, specialist or as an experienced professional.
You are used to creating results in projects. To succeed, you must thrive in a role where you take leadership, initiate and coordinate a large number of actions and projects. You thrive by challenging the managers in good GMP practise. You know how to anchor your solutions into systems and this requires an excellent overview, a structured mind-set and way of working. 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 Anne Reker Cordt at +45 3079 9308.
Deadline
10 January 2014
- Production
- Denmark - Hillerød
Are you ready to take the next step in your career - you now have the opportunity!!
You will be key player in ensuring quality and compliance for a large business area in Site Hillerød consisting 5 departments, more than 20 managers and app. 350 employees. You will be a key member of the ambitious, local management team and primary sparring partner for the Vice President and directors on critical GMP issues.
About the department
We are looking for GMP Partners to our sites in Hillerød 25A where we focus on both aseptic production and on medical devices. The GMP-partner and coordinator setup is a matrix organisation, where you will head up 5 GMP Coordinators across the different departments.
The job
As GMP Partner you have the overall responsibility for setting the targets on quality 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 common 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 Site Denmark’s 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 SDKs GMP network meetings with your peers for sparring, sharing and development of GMP and QMS related topics. The network is owned and facilitated by the QMS function.
The job involves contact and interaction to many different stakeholders in the organisation, from operators, maintenance, cLEAN professionals, project managers and to all line management levels. Your role calls for strong change management and communication skills and ability to create the right quality and compliance mindset.
Qualifications
You hold a degree at minimum master’s level. Your academic background is topped with experience from a pharmaceutical production where you have gained solid experience within quality, GMP and ISO9001. Maybe you already work in Novo Nordisk as a manager, project manager, specialist or as an experienced professional.
You are used to creating results in projects. To succeed, you must thrive in a role where you take leadership, initiate and coordinate a large number of actions and projects. You thrive by challenging the managers in good GMP practise. You know how to anchor your solutions into systems and this requires an excellent overview, a structured mind-set and way of working. 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 Anne Reker Cordt at +45 3079 9308.
Deadline
10 January 2014