Enthusiastic GMP Supporter
- Quality, senior position
- Denmark - Gentofte
Are you ready to take up the challenge to be the one securing and enhancing the quality and compliance level of a production environment? We are looking for a GMP Supporter with the skills, knowledge and overview to secure the department’s GMP and compliance level, making it ready for inspection at all times.
About the department
You will join a high-tech filling factory in Gentofte, where we produce NovoSeven®, GlucaGen® and other Biopharm products. Our responsibilities include: wash and sterilisation of equipment, formulation, sterile filtration, sterile filling, freeze drying and visual inspection.As a GMP Supporter you will join the management team consisting of two 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.
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 join the support function, 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
Besides your relevant education as engineer, pharmacist, cand. scient or similar, it is important that you have a strong sense of quality and experience working with GMP. You have experience working with LEAN tools, preferable in relation to non-conformity investigations.As a person you are a problem solver and you thrive in a dynamic work environment. You are able to make decisions in complex situations. Because quality and precision is essential for the pharmaceutical industry, it is important that you have a high sense of quality. You are able to communicate and be accurate in writing and speaking in both Danish and English. At last but not at least you are out going and enjoy building relations with stakeholders across functional areas and at any organisational level.
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.
Contact
For further information, please Contact Søren Karmdal on + 45 3079 1257.
Deadline
21 November 2013.
- Quality, senior position
- Denmark - Gentofte
Are you ready to take up the challenge to be the one securing and enhancing the quality and compliance level of a production environment? We are looking for a GMP Supporter with the skills, knowledge and overview to secure the department’s GMP and compliance level, making it ready for inspection at all times.
About the department
You will join a high-tech filling factory in Gentofte, where we produce NovoSeven®, GlucaGen® and other Biopharm products. Our responsibilities include: wash and sterilisation of equipment, formulation, sterile filtration, sterile filling, freeze drying and visual inspection.As a GMP Supporter you will join the management team consisting of two 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.
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 join the support function, 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
Besides your relevant education as engineer, pharmacist, cand. scient or similar, it is important that you have a strong sense of quality and experience working with GMP. You have experience working with LEAN tools, preferable in relation to non-conformity investigations.As a person you are a problem solver and you thrive in a dynamic work environment. You are able to make decisions in complex situations. Because quality and precision is essential for the pharmaceutical industry, it is important that you have a high sense of quality. You are able to communicate and be accurate in writing and speaking in both Danish and English. At last but not at least you are out going and enjoy building relations with stakeholders across functional areas and at any organisational level.
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.
Contact
For further information, please Contact Søren Karmdal on + 45 3079 1257.
Deadline
21 November 2013.