Dynamic Quality Consultant for manufacturing
- Quality, senior position
- Denmark - Gentofte
We seek a Quality Consultant to ensure that our work is compliant with GMP and in line with Novo Nordisk QMS and to ensure that our aseptic production is in compliance with regulatory requirements.
About the department
Our department covers the complete API manufacturing process, from fermentation and recovery to liquid purification and freeze drying. We are organized in four teams, where two teams cover production (fermentation and purification) and two support teams.As a GMP Consultant you will join the management team consisting of four team leaders, two specialists and the department manager to whom you will report directly. You will be the primary responsible for the ensuring the compliance level which will be one of the primary focus areas in the department in the coming years.You will become part of a team which have a high level of self-governance. The working relations are informal and the team value professional sparring and good humour highly.
The Job
Together with the Management team you will be responsible for ensuring that we comply with Novo Nordisk’s quality system. As such, you participate in determining the quality objectives, and through planning and follow-up on quality activity plans and conduction of quality management reviews you ensure that the standards are met. In this respect, you will cooperate across the entire area and have close interaction with Quality Assurance. In this way, you provide sparring and consulting on quality and compliance inquires, as well as you interpret processes and come up with quality enhancing initiatives on the problems and improvements that you face in your everyday.In addition, you will drive and coordinate the quality work and secure continuous improvements of audits and inspections, as well as you coordinate and conduct training within GMP.
Qualifications
You hold an academic degree (e.g. engineer, chemist or pharmacist), and you have more than 2-3 years of practical experience with GMP and ISO9001 in pharmaceutical production or QA. You might even have experience with line management and/or project management, and are capable of working in all levels of the organisation. You take pride in reaching you targets on time, and are able to do so with limited guidance from your superior.
As a person you have an infectious energy and a drive for creating results in close cooperation with others. You have daily contact with many different types of employees, and the ability to communicate and create strong relations is therefore a necessity in order to be successful in the position as GMP consultant.
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.
Feel free to submit your job application in either English or Danish, whichever you prefer. Applications are reviewed on a rolling basis so please apply as soon as possible.
Contact
For further information, please Contact Søren Jensen on + 45 3079 1257.
Deadline
26 November 2013.
- Quality, senior position
- Denmark - Gentofte
We seek a Quality Consultant to ensure that our work is compliant with GMP and in line with Novo Nordisk QMS and to ensure that our aseptic production is in compliance with regulatory requirements.
About the department
Our department covers the complete API manufacturing process, from fermentation and recovery to liquid purification and freeze drying. We are organized in four teams, where two teams cover production (fermentation and purification) and two support teams.As a GMP Consultant you will join the management team consisting of four team leaders, two specialists and the department manager to whom you will report directly. You will be the primary responsible for the ensuring the compliance level which will be one of the primary focus areas in the department in the coming years.You will become part of a team which have a high level of self-governance. The working relations are informal and the team value professional sparring and good humour highly.
The Job
Together with the Management team you will be responsible for ensuring that we comply with Novo Nordisk’s quality system. As such, you participate in determining the quality objectives, and through planning and follow-up on quality activity plans and conduction of quality management reviews you ensure that the standards are met. In this respect, you will cooperate across the entire area and have close interaction with Quality Assurance. In this way, you provide sparring and consulting on quality and compliance inquires, as well as you interpret processes and come up with quality enhancing initiatives on the problems and improvements that you face in your everyday.In addition, you will drive and coordinate the quality work and secure continuous improvements of audits and inspections, as well as you coordinate and conduct training within GMP.
Qualifications
You hold an academic degree (e.g. engineer, chemist or pharmacist), and you have more than 2-3 years of practical experience with GMP and ISO9001 in pharmaceutical production or QA. You might even have experience with line management and/or project management, and are capable of working in all levels of the organisation. You take pride in reaching you targets on time, and are able to do so with limited guidance from your superior.
As a person you have an infectious energy and a drive for creating results in close cooperation with others. You have daily contact with many different types of employees, and the ability to communicate and create strong relations is therefore a necessity in order to be successful in the position as GMP consultant.
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.
Feel free to submit your job application in either English or Danish, whichever you prefer. Applications are reviewed on a rolling basis so please apply as soon as possible.
Contact
For further information, please Contact Søren Jensen on + 45 3079 1257.
Deadline
26 November 2013.