HPLC QC Chemist with extensive GMP experience
- Quality
- Denmark - Gentofte
Do you want to be a part of a team in growth? Are you customer orientated and do you want to ensure the right quality of analysis in Biopharm? Then you might be our new colleague for a two year temporary position.
About the department
Biopharm QC Chemistry performs chemical and biological analysis on finished products, API, and handles stability studies and customer complaints, covering several biopharmaceutical products.
The department consists of about 80 dedicated employees divided into four teams. We have a busy and stimulating working environment with lots of opportunities to develop both your professional and personal competencies. The position is placed in one of our two HPLC teams. Today the HPLC team consists of 10 laboratory technicians, 5 chemists and 1 Associate Manager. The main responsibilities for the team are HPLC and GC analysis on Norditropin and Glucagon.
The Job
As a QC Chemist you will be one of the key players in securing compliance and you will be a part of the daily operation from analysis to result release on product. You have to be able to evaluate and solve challenges via your scientific skills and your solid knowledge within GMP compliance. It is important that you can handle several tasks at ones and be able to finish them timely. Typical daily tasks could be release of analytical results, handling of non-conformities, laboratory investigations and change requests as well as many different types of compliance projects.
Qualifications
You have an academic degree (Cand. Pharm, chemical engineer, biochemist, or other equivalent level of education) and you have several years of experience with GMP and the requirements of the authorities in the pharmaceutical industry.
You have experience working with HPLC and you are familiar with qualification of equipment and validation. You are experienced with Lean and one of your strengths is your analytic ability to perform systematic troubleshooting. You are fluent in Danish and English both spoken and written and you have flair for preparing documentation. You possess good communication skills and will be able to present documentation at inspections.
Contact
You have a strong quality mind-set. You are open minded and engaged and you are capable of motivating and inspiring your colleagues. You keep a sense of perspective and high spirits in a busy working environment. You work in a structured and systematic way and are used to deliver according to targets.
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 Anders W. Nielsen on +45 3075 9440.
Deadline
05 January 2014.
- Quality
- Denmark - Gentofte
Do you want to be a part of a team in growth? Are you customer orientated and do you want to ensure the right quality of analysis in Biopharm? Then you might be our new colleague for a two year temporary position.
About the department
Biopharm QC Chemistry performs chemical and biological analysis on finished products, API, and handles stability studies and customer complaints, covering several biopharmaceutical products.
The department consists of about 80 dedicated employees divided into four teams. We have a busy and stimulating working environment with lots of opportunities to develop both your professional and personal competencies. The position is placed in one of our two HPLC teams. Today the HPLC team consists of 10 laboratory technicians, 5 chemists and 1 Associate Manager. The main responsibilities for the team are HPLC and GC analysis on Norditropin and Glucagon.
The Job
As a QC Chemist you will be one of the key players in securing compliance and you will be a part of the daily operation from analysis to result release on product. You have to be able to evaluate and solve challenges via your scientific skills and your solid knowledge within GMP compliance. It is important that you can handle several tasks at ones and be able to finish them timely. Typical daily tasks could be release of analytical results, handling of non-conformities, laboratory investigations and change requests as well as many different types of compliance projects.
Qualifications
You have an academic degree (Cand. Pharm, chemical engineer, biochemist, or other equivalent level of education) and you have several years of experience with GMP and the requirements of the authorities in the pharmaceutical industry.
You have experience working with HPLC and you are familiar with qualification of equipment and validation. You are experienced with Lean and one of your strengths is your analytic ability to perform systematic troubleshooting. You are fluent in Danish and English both spoken and written and you have flair for preparing documentation. You possess good communication skills and will be able to present documentation at inspections.
Contact
You have a strong quality mind-set. You are open minded and engaged and you are capable of motivating and inspiring your colleagues. You keep a sense of perspective and high spirits in a busy working environment. You work in a structured and systematic way and are used to deliver according to targets.
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 Anders W. Nielsen on +45 3075 9440.
Deadline
05 January 2014.