QA Associate Manager
- Quality
- Denmark - Gentofte
Do you want responsibility for developing people and optimizing processes in a core part of Novo Nordisk’s QA organization? You will be leading a highly competent QA team of 8 employees responsible for the quality assurance of Biopharm Manufacturing Development. Since the team is newly established, we are now looking for a new colleague to lead the team.
About the department
“Biopharm QA QC & Support” consists of two teams, one responsible for quality assurance of QC analyses and the other responsible for quality assurance of development activities. Our key tasks are to review and approve GMP documentation such as validation reports, change requests and non-conformities in order to be able to insure delivery of high quality products in compliance.
The Job
As Associate Manager in Biopharm QA Support team you will be the leader of 8 highly skilled and motivated QA professionals, forming a new team since 1 November 2013. The team provides quality assurance for the manufacturing development activities in Biopharm and as associate manager you will be involved both as QA person handling cases and as a representative of the department manager. You set a good example and lead the way to ensure that your employees obtain the right behaviour and achieve the targets all to the benefit of our patients. You act as a competent sparring partner to your team you coach and empower your employees to deliver excellent results. You collaborate with the Manufacturing Development departments in a professional and amicable way and collaborate to overcome disagreements while never compromising on quality mindset and compliance.
Qualifications
You have a solid working experience from a QA organization which ideally is from a similar role in a pharmaceutical company and your experience is paired with a relevant Master of Science degree. You set and communicate a clear direction for your team. You display a high level of personal engagement, drive, persistence and integrity. Precise communication is essential and you must be capable of taking part in constructive cooperation concerning the various tasks and have the kind of impact that means that you can stand firm in favour of product and user safety, as well as compliance. Your language skills cover proficiency in both Danish and English.
Feel free to submit your job application in either English or Danish, whichever you prefer.
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 contact Ulla Thinggaard at +45 3075 2104.
Deadline
03 January 2014
- Quality
- Denmark - Gentofte
Do you want responsibility for developing people and optimizing processes in a core part of Novo Nordisk’s QA organization? You will be leading a highly competent QA team of 8 employees responsible for the quality assurance of Biopharm Manufacturing Development. Since the team is newly established, we are now looking for a new colleague to lead the team.
About the department
“Biopharm QA QC & Support” consists of two teams, one responsible for quality assurance of QC analyses and the other responsible for quality assurance of development activities. Our key tasks are to review and approve GMP documentation such as validation reports, change requests and non-conformities in order to be able to insure delivery of high quality products in compliance.
The Job
As Associate Manager in Biopharm QA Support team you will be the leader of 8 highly skilled and motivated QA professionals, forming a new team since 1 November 2013. The team provides quality assurance for the manufacturing development activities in Biopharm and as associate manager you will be involved both as QA person handling cases and as a representative of the department manager. You set a good example and lead the way to ensure that your employees obtain the right behaviour and achieve the targets all to the benefit of our patients. You act as a competent sparring partner to your team you coach and empower your employees to deliver excellent results. You collaborate with the Manufacturing Development departments in a professional and amicable way and collaborate to overcome disagreements while never compromising on quality mindset and compliance.
Qualifications
You have a solid working experience from a QA organization which ideally is from a similar role in a pharmaceutical company and your experience is paired with a relevant Master of Science degree. You set and communicate a clear direction for your team. You display a high level of personal engagement, drive, persistence and integrity. Precise communication is essential and you must be capable of taking part in constructive cooperation concerning the various tasks and have the kind of impact that means that you can stand firm in favour of product and user safety, as well as compliance. Your language skills cover proficiency in both Danish and English.
Feel free to submit your job application in either English or Danish, whichever you prefer.
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 contact Ulla Thinggaard at +45 3075 2104.
Deadline
03 January 2014