Analytical Research Scientist
- Research & Development
- Denmark - Måløv
A challenging and varied position in CMC Analytical Development is available for a dynamic and skilful scientist within a R&D analytical support laboratory.
About the department
Department Diabetes Analytical Development is a part of CMC Injectable Protein Formulation in R&D. The department are organised in two analytical teams with a total number of 29 persons. The open position is in team Diabetes Analytical Support, which consists of 2 scientists and 11 technicians. Acting as link between Research Unit and Production the department is responsible for developing and supporting analytical methods for new diabetes products – all the way from early development until phase 3. The team is responsible for app. 50 different analytical methods, on a platform mainly of chromatographic methods within HPLC and UPLC.
The job
As Research Scientist you hold the analytical responsibility of a number of analytical methods. We continuously improve our processes and have a structured approach to problem solving through cLEAN. Trouble-shooting, interaction and daily supervision of the technicians are some of the exciting daily challenges. Therefore, an interest in leadership is an advantage. Furthermore you will interact with a wide variety of internal stakeholders, e.g. API Process Development, Analytical Formulation Development and Quality Assurance.
Qualifications
You hold a Master’s degree within Life Sciences (Pharmacy, Engineering or other relevant discipline). You have a minimum of 2 years of practical experience within HPLC/UPLC analytical development in the pharmaceutical industry. You have a good knowledge of general protein chemistry, and HPLC/UPLC. Knowledge of GMP/GLP regulatory requirements is an asset.
As person you have a positive and flexible mind-set, which is helpful in an ever changing project environment and enabling you to build fruitful relations to colleagues and stakeholders. You are a team player and contribute to reaching team goals. You have excellent oral and written communication skills. Preferably you have a growing intest for leadership, planning and coordination.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Karoline Benktander at +45 3075 8013.
Deadline
18 August 2013.
- Research & Development
- Denmark - Måløv
A challenging and varied position in CMC Analytical Development is available for a dynamic and skilful scientist within a R&D analytical support laboratory.
About the department
Department Diabetes Analytical Development is a part of CMC Injectable Protein Formulation in R&D. The department are organised in two analytical teams with a total number of 29 persons. The open position is in team Diabetes Analytical Support, which consists of 2 scientists and 11 technicians. Acting as link between Research Unit and Production the department is responsible for developing and supporting analytical methods for new diabetes products – all the way from early development until phase 3. The team is responsible for app. 50 different analytical methods, on a platform mainly of chromatographic methods within HPLC and UPLC.
The job
As Research Scientist you hold the analytical responsibility of a number of analytical methods. We continuously improve our processes and have a structured approach to problem solving through cLEAN. Trouble-shooting, interaction and daily supervision of the technicians are some of the exciting daily challenges. Therefore, an interest in leadership is an advantage. Furthermore you will interact with a wide variety of internal stakeholders, e.g. API Process Development, Analytical Formulation Development and Quality Assurance.
Qualifications
You hold a Master’s degree within Life Sciences (Pharmacy, Engineering or other relevant discipline). You have a minimum of 2 years of practical experience within HPLC/UPLC analytical development in the pharmaceutical industry. You have a good knowledge of general protein chemistry, and HPLC/UPLC. Knowledge of GMP/GLP regulatory requirements is an asset.
As person you have a positive and flexible mind-set, which is helpful in an ever changing project environment and enabling you to build fruitful relations to colleagues and stakeholders. You are a team player and contribute to reaching team goals. You have excellent oral and written communication skills. Preferably you have a growing intest for leadership, planning and coordination.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Karoline Benktander at +45 3075 8013.
Deadline
18 August 2013.