Chemist HPLC-2
- Production
- Denmark - Gentofte
Are you our new scientific colleague in the dynamic HPLC team at Novo Nordisk in Gentofte? We are in rapid growth, working with the quality control of Biopharm’s broad portfolio of haemophilia products, and therefore we urgently need your solid HPLC and GMP insight.
About the department
The department validates the analytical methods for the new haemophilia products and the release testing of clinical phase 3 batches. In addition we support the three chemical site QC laboratories in Biopharm using our technical skills combined with systematic problem solving.
We work in an unpretentious and good atmosphere with knowledge share across teams and professional groups.
The job
You and your 16 colleagues share the responsibility for the day-to-day running of our HPLC methods and ensure that the analytical results comply with the current GMP standards. You will approve the analytical results and troubleshoot on the methods of analyses, and at the same time prepare instructions, non-conformity reports and change requests. Another part of your responsibility covers standardisation and optimisation of HPLC methods. You will participate in cross-organisational meetings and as such be in close dialogue with the development laboratories. In case of deviations, it is your job to go into dialogue with our colleagues in the production. Together you examine the cause and analyse the problem further, before you make your suggestion for solution of the incident. As such you will have a challenging and innovative job that requires your energetic, dynamic and flexible mindset.
Qualifications
You hold a Master of Pharmacy, Cand Scient or similar and have a solid HPLC background from several years in a GMP-controlled environment. Here you have been part of another busy environment, and you thrive in an unpredictable workday where you solve heavy challenges and adjust tiny details. You have extensive experience in validation and standardisation of HPLC analyses and you are able to create a crystal clear overview and prioritise your tasks – even when deadlines are closing in. You never compromise on quality, however, you are able to round off and finish your tasks on time in order to proceed to the next assignment with enthusiasm and energy. Besides being open-minded and committed, you know how to motivate and inspire your colleagues to perform even better. You use your LEAN knowledge to renew our work processes, and you follow a systematic and analytic practice in order to meet the many deadlines. Lastly, you speak and write Danish and English fluently.
In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
We will interview candidates continually as we receive the applications. Deadline for application is 1 September
Contact
For further information, please contact Christina Alsted Frandsen at +45 3075 6552.
Deadline
1 September 2013.
- Production
- Denmark - Gentofte
Are you our new scientific colleague in the dynamic HPLC team at Novo Nordisk in Gentofte? We are in rapid growth, working with the quality control of Biopharm’s broad portfolio of haemophilia products, and therefore we urgently need your solid HPLC and GMP insight.
About the department
The department validates the analytical methods for the new haemophilia products and the release testing of clinical phase 3 batches. In addition we support the three chemical site QC laboratories in Biopharm using our technical skills combined with systematic problem solving.
We work in an unpretentious and good atmosphere with knowledge share across teams and professional groups.
The job
You and your 16 colleagues share the responsibility for the day-to-day running of our HPLC methods and ensure that the analytical results comply with the current GMP standards. You will approve the analytical results and troubleshoot on the methods of analyses, and at the same time prepare instructions, non-conformity reports and change requests. Another part of your responsibility covers standardisation and optimisation of HPLC methods. You will participate in cross-organisational meetings and as such be in close dialogue with the development laboratories. In case of deviations, it is your job to go into dialogue with our colleagues in the production. Together you examine the cause and analyse the problem further, before you make your suggestion for solution of the incident. As such you will have a challenging and innovative job that requires your energetic, dynamic and flexible mindset.
Qualifications
You hold a Master of Pharmacy, Cand Scient or similar and have a solid HPLC background from several years in a GMP-controlled environment. Here you have been part of another busy environment, and you thrive in an unpredictable workday where you solve heavy challenges and adjust tiny details. You have extensive experience in validation and standardisation of HPLC analyses and you are able to create a crystal clear overview and prioritise your tasks – even when deadlines are closing in. You never compromise on quality, however, you are able to round off and finish your tasks on time in order to proceed to the next assignment with enthusiasm and energy. Besides being open-minded and committed, you know how to motivate and inspire your colleagues to perform even better. You use your LEAN knowledge to renew our work processes, and you follow a systematic and analytic practice in order to meet the many deadlines. Lastly, you speak and write Danish and English fluently.
In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
We will interview candidates continually as we receive the applications. Deadline for application is 1 September
Contact
For further information, please contact Christina Alsted Frandsen at +45 3075 6552.
Deadline
1 September 2013.