Analytical Scientist for Drug Product Development in R&D
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Måløv
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- Måløv
Do you have the expertise 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 scientific skills and stakeholder management? If so, you may be our new analytical scientist.
About the department
The Department CMC Analytical Development is part of Chemical Manufacturing Control (CMC) Drug Product (DP) development in R&D Novo Nordisk A/S. The department is organised in 3 highly skilled analytical teams with a total of 57 employees. Two teams analyse all drug product and drug substance samples including all GMP activities and one team is responsible for development and operates in a GSP environment. The department is responsible for developing analytical methods, including validation and documentation, and delivering analytical results for new drug substance and drug product – thereby 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.
The Job
As analytical scientist in the development team, you will be joining a great team of dedicated and experienced colleagues, both scientists and laboratory technicians. Your responsibility covers analytical development and optimization of analytical methods within drug substance and injectable products with a special focus on chromatographic methods (HPLC/UPLC).
You will plan and coordinate experiments for method development and you will be the responsible analytical person in the projects. This will involve a close collaboration with scientists and technicians in- and outside the department.
On an ongoing basis, you will also take responsibility for ensuring that the equipment is functioning for the purpose. Troubleshooting of analytical equipment and methods, including driving optimization of both processes and systems will therefore be a key part of your responsibility.
Qualifications
You hold a Master’s degree within Life Sciences (Pharmacy, Engineering or other relevant discipline) together with a PhD or similar experience. You have several years’ experience within HPLC/UPLC and LC-MS analytical development within the pharmaceutical industry and a keen interest in understanding and optimizing equipment. You have good knowledge of general protein chemistry and a natural flair for thinking in new solutions. Furthermore, it is essential that stakeholder management is part of your DNA as this is very important to succeed in the job.
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. Finally, you are a team player and contribute to reach our team goals.
Contact
For further information, please contact Anders Bach Nielsen +45 3075 3889
Deadline
6th of February 2020
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 16.1.2020, 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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