Research Scientist
- Research & Development
- Denmark - Gentofte
Would you like to work with formulation development in a team dedicated to developing the next generation of biopharmaceuticals – then we have the job for you!
A challenging position in team Biopharm Formulation Development II is available for a dynamic and skilful scientist within formulation development of biopharmaceuticals.
About the department
Biopharm Formulation Development is part of Injectable Protein Formulation in the R&D area CMC Supply. The department is responsible for formulation development of new biopharmaceutical drug products - primarily soluble and freeze-dried injectables of new therapeutic proteins and monoclonal antibodies. We are involved in development and research projects mainly within haemostasis and inflammation. We are located in Gentofte (Copenhagen, Denmark), and right now we are facing new exiting challenges due to our rapidly increasing project portfolio.
The job
In the team we are 8 Technicians, 6 Scientists/Specialists and a Team Leader. As formulation scientist in team Biopharm Formulation Development II you are responsible for development of stable protein formulations with optimal biopharmaceutical characteristics within our monoclonal antibody and growth hormone portfolio. You work in a team and you will design, interpret and report studies on drug product - hereby generating pharmaceutical documentation for internal and external use. You will interact with a wide variety of internal stakeholders, e.g. Analytical Development, Production Pilot Plant, Quality Assurance and Regulatory affairs.
Qualifications
You hold a Master of Science possibly combined with a PhD in Chemical Engineering, Pharmacy or another relevant scientific discipline. You have working experience within drug product development. It is an advantage if you have working knowledge of the documentation requirements for biopharmaceutical drug products across the development phases. As a person you are result-oriented and flexible. You enjoy working in a team with highly motivated people, dedicated to developing the next generation of biopharmaceuticals. You work systematically, have good collaborative skills and are used to adhering to strict documentation standards. You possess drive and a positive mindset, and you strive to be in a decision-making role. When cooperating you often take the leading role and you enjoy setting direction to others.
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 Anne Mette Beier at + 45 3079 8535.
Deadline
31 December 2013.
- Research & Development
- Denmark - Gentofte
Would you like to work with formulation development in a team dedicated to developing the next generation of biopharmaceuticals – then we have the job for you!
A challenging position in team Biopharm Formulation Development II is available for a dynamic and skilful scientist within formulation development of biopharmaceuticals.
About the department
Biopharm Formulation Development is part of Injectable Protein Formulation in the R&D area CMC Supply. The department is responsible for formulation development of new biopharmaceutical drug products - primarily soluble and freeze-dried injectables of new therapeutic proteins and monoclonal antibodies. We are involved in development and research projects mainly within haemostasis and inflammation. We are located in Gentofte (Copenhagen, Denmark), and right now we are facing new exiting challenges due to our rapidly increasing project portfolio.
The job
In the team we are 8 Technicians, 6 Scientists/Specialists and a Team Leader. As formulation scientist in team Biopharm Formulation Development II you are responsible for development of stable protein formulations with optimal biopharmaceutical characteristics within our monoclonal antibody and growth hormone portfolio. You work in a team and you will design, interpret and report studies on drug product - hereby generating pharmaceutical documentation for internal and external use. You will interact with a wide variety of internal stakeholders, e.g. Analytical Development, Production Pilot Plant, Quality Assurance and Regulatory affairs.
Qualifications
You hold a Master of Science possibly combined with a PhD in Chemical Engineering, Pharmacy or another relevant scientific discipline. You have working experience within drug product development. It is an advantage if you have working knowledge of the documentation requirements for biopharmaceutical drug products across the development phases. As a person you are result-oriented and flexible. You enjoy working in a team with highly motivated people, dedicated to developing the next generation of biopharmaceuticals. You work systematically, have good collaborative skills and are used to adhering to strict documentation standards. You possess drive and a positive mindset, and you strive to be in a decision-making role. When cooperating you often take the leading role and you enjoy setting direction to others.
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 Anne Mette Beier at + 45 3079 8535.
Deadline
31 December 2013.