Temporary Research Scientist
- Research & Development
- Denmark - Måløv
Do you have the knowledge and experience it takes to break new land and develop the diabetes products of the future? If so, you have the opportunity to play a key role in CMC Diabetes Formulation Development in Måløv, Copenhagen. As the link between the research unit and the production we are responsible for developing subcutaneous injection formulations and processes all the way from early development to phase III clinical trials and registration.
About the department
We are organised in two formulation teams with a total number of 30 persons. You will be part of the team that is responsible for formulation development/support of non clinical material and product development including stability and clinical trial documentation.
The job
The job is a temporary position with the duration of 12 months. In this job you will be the driver of cross organisational project deliverables such as nonclinical formulation development/support and stability of both non clinical and clinical drug product, which includes writing filing and clinical trial documentation. Beside this you will also be responsible for general tasks such as ongoing optimisation of processes and systems with LEAN as the guiding light. You will work in a series of multidisciplinary project groups closely allied with Research, Nonclinical, Analytical, Regulatory, Quality and GMP production departments. When working cross organisationally, you will represent the protein formulation field. The goal is clear: to develop the next generation of products for diabetes treatment.
Qualifications
You have a Master or PhD within Pharmacy, Engineering or related field of study. This is backed by some years of practical experience within pharmaceutical R&D work, including experience with regulatory and quality aspects of R&D projects. You have good knowledge of protein/peptide formulations and process development and work independently. Working cross organisationally and multidisciplinary, you must possess a proper understanding of the pharmaceutical development process. As person you have a positive and objective mindset enabling you to build fruitful relations to colleagues and partners. As part of this, you thrive on being the inspirer to your colleagues.
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 Thomas Falck at +45 3075 7650 or Rozana Sten at +45 3075 2472.
Deadline
12 August 2013.
- Research & Development
- Denmark - Måløv
Do you have the knowledge and experience it takes to break new land and develop the diabetes products of the future? If so, you have the opportunity to play a key role in CMC Diabetes Formulation Development in Måløv, Copenhagen. As the link between the research unit and the production we are responsible for developing subcutaneous injection formulations and processes all the way from early development to phase III clinical trials and registration.
About the department
We are organised in two formulation teams with a total number of 30 persons. You will be part of the team that is responsible for formulation development/support of non clinical material and product development including stability and clinical trial documentation.
The job
The job is a temporary position with the duration of 12 months. In this job you will be the driver of cross organisational project deliverables such as nonclinical formulation development/support and stability of both non clinical and clinical drug product, which includes writing filing and clinical trial documentation. Beside this you will also be responsible for general tasks such as ongoing optimisation of processes and systems with LEAN as the guiding light. You will work in a series of multidisciplinary project groups closely allied with Research, Nonclinical, Analytical, Regulatory, Quality and GMP production departments. When working cross organisationally, you will represent the protein formulation field. The goal is clear: to develop the next generation of products for diabetes treatment.
Qualifications
You have a Master or PhD within Pharmacy, Engineering or related field of study. This is backed by some years of practical experience within pharmaceutical R&D work, including experience with regulatory and quality aspects of R&D projects. You have good knowledge of protein/peptide formulations and process development and work independently. Working cross organisationally and multidisciplinary, you must possess a proper understanding of the pharmaceutical development process. As person you have a positive and objective mindset enabling you to build fruitful relations to colleagues and partners. As part of this, you thrive on being the inspirer to your colleagues.
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 Thomas Falck at +45 3075 7650 or Rozana Sten at +45 3075 2472.
Deadline
12 August 2013.