Analytical Scientist in R&D
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Måløv
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- Måløv
Do you have the knowledge to contribute to the development and documentation of analytical methods for future diabetes, bleeding disorders and obesity products? And do you enjoy working in an open, dynamic and social atmosphere with a strong focus on technical and scientific skills? If so, you may be our new analytical scientist.
About the department
The Department CMC Analytical Development is part of CMC DP development in R&D Novo Nordisk A/S. The department is organised in 3 highly skilled analytical teams with a total of 60 employees. The 3 teams are divided in two teams that analyse all drug product and drug substance samples including all GMP and one development team that operates in a GSP environment. The department is responsible for developing analytical methods, validation, documentation and delivering analytical results for new drug substance and drug product - acting as the link between the research unit and the production, all the way from early development to phase 3 clinical trials and registration. The analytical platform is primarily based on HPLC/UPLC and LC-MS but also include iCIEF, CE-SDS, pH and appearance.
The Job
You will be part of the Analytical Development team and the focus will be to document and optimise analytical methods within drug substance and injectable products. Together with our skilled technicians you will be responsible for planning and coordinating experiments for method development and you will be the responsible analytical person in the projects. Therefore, you will naturally have a close collaboration with many scientists and technicians in- and outside the department. You will also be responsible for troubleshooting of analytical equipment and methods. Finally, together with your colleagues you will contribute to the on-going optimization and digitalisation of processes and systems.
Qualifications
You hold a Master’s degree within Life Sciences (Pharmacy, Engineering or other relevant discipline) and a PhD or similar experience. You have practical experience within HPLC/UPLC and LC-MS analytical development preferably within the pharmaceutical industry and knowledge of iCIEF and CE-SDS is an advantage. You have good knowledge of general protein chemistry and a natural flair for thinking in new solutions and automation. Furthermore, programming and mathematic modelling skills are preferred.
As a person you have a positive and flexible mind-set, which is helpful in an ever-changing project environment. You have excellent interpersonal skills that allow you to build fruitful relations to both colleagues and stakeholders. You are a team player and contribute to reaching team goals, and you have excellent oral and written communication skills. You master both English and a Scandinavian language (Swedish, Danish or Norwegian).
Contact
For further information, please contact Anders Bach Nielsen +45 3075 3889
We review applications and invite for interviews on a continuous basis.
Deadline
4th of August 2019.
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
Information og data
Denne ledige stilling har jobtypen "Forsker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 25.6.2019, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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