Chemist
- Quality
- Denmark - Bagsværd
Do you want to manage and improve a variety of material analyses in a highly professional QC laboratory? In that case you should apply for the new position as Chemist in QC Raw Materials. If you are as ambitious as we are, you can look forward to an exciting job in an environment where we seek to be best in class in everything we do.
About the department
Your new department, QC Raw Materials, consists of 59 employees who are located in Bagsværd and Kalundborg. You will join the analytical team in Bagsværd, which is responsible for the chemical control of raw materials for the production across Novo Nordisk. We cooperate with a variety of functions, including purchase, storage and QA.
The Job
You will work closely with the chemists and laboratory technicians in your team to approve the raw materials and thereby enable a continuously high pace in the production. You will be responsible for several analytical methods and for securing that the analytical flow is aligned with our customers’ expectations along with regulatory compliance. Your primary focus will be chromatographic analyses (HPLC and GC-MS) however a broad understanding of analytical methods is an advantage. You will among other things be responsible of method development and validation, pharmacopeial monitoring and updates, handling of change requests, non-conformities and OOS. A high GMP and compliance mind-set is thus required. In general, the assignments carried out by the department are diverse as we deliver to various parts of Novo Nordisk. This gives a variety of analytical challenges and strong collaboration with your colleagues is therefore an essential key to success.
You will further support the laboratory technicians in their daily operations to ensure that the analytical performance and equipment live up to the industry standard.
Qualifications
You hold an MSc in Pharmacy, Engineering or another relevant field within the natural sciences. Your degree is supplemented with several years of experience from a similar job in which you have gained in-depth knowledge of working with GMP in a laboratory environment. Strong practical and theoretical experience within chromatographic analyses will be required. You have a high level of energy to drive yourself and your colleagues forward. You are result-oriented and take pride in delivering on your milestones, and you motivate your colleagues with a positive, forthcoming attitude. You work well independently, although it also motivates you to cooperate with colleagues and stakeholders across functions and departments. Lastly, you must have fluency in written and spoken Danish and English.
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 Jacob Kirkegaard Jensen at +45 3075 6914.
Deadline
1 December 2013
- Quality
- Denmark - Bagsværd
Do you want to manage and improve a variety of material analyses in a highly professional QC laboratory? In that case you should apply for the new position as Chemist in QC Raw Materials. If you are as ambitious as we are, you can look forward to an exciting job in an environment where we seek to be best in class in everything we do.
About the department
Your new department, QC Raw Materials, consists of 59 employees who are located in Bagsværd and Kalundborg. You will join the analytical team in Bagsværd, which is responsible for the chemical control of raw materials for the production across Novo Nordisk. We cooperate with a variety of functions, including purchase, storage and QA.
The Job
You will work closely with the chemists and laboratory technicians in your team to approve the raw materials and thereby enable a continuously high pace in the production. You will be responsible for several analytical methods and for securing that the analytical flow is aligned with our customers’ expectations along with regulatory compliance. Your primary focus will be chromatographic analyses (HPLC and GC-MS) however a broad understanding of analytical methods is an advantage. You will among other things be responsible of method development and validation, pharmacopeial monitoring and updates, handling of change requests, non-conformities and OOS. A high GMP and compliance mind-set is thus required. In general, the assignments carried out by the department are diverse as we deliver to various parts of Novo Nordisk. This gives a variety of analytical challenges and strong collaboration with your colleagues is therefore an essential key to success.
You will further support the laboratory technicians in their daily operations to ensure that the analytical performance and equipment live up to the industry standard.
Qualifications
You hold an MSc in Pharmacy, Engineering or another relevant field within the natural sciences. Your degree is supplemented with several years of experience from a similar job in which you have gained in-depth knowledge of working with GMP in a laboratory environment. Strong practical and theoretical experience within chromatographic analyses will be required. You have a high level of energy to drive yourself and your colleagues forward. You are result-oriented and take pride in delivering on your milestones, and you motivate your colleagues with a positive, forthcoming attitude. You work well independently, although it also motivates you to cooperate with colleagues and stakeholders across functions and departments. Lastly, you must have fluency in written and spoken Danish and English.
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 Jacob Kirkegaard Jensen at +45 3075 6914.
Deadline
1 December 2013