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Research Scientist to Injectable Formulation & Process Development

Do you have the knowledge and experience it takes to break new land and develop diabetes and biopharm products of the future? As the link between our research unit and our production we are responsible for developing formulation and processes for new injectable products all the way from early development to phase III clinical trials and registration. So if you find this exciting please keep reading!

About the department
Injectable Formulation & Process Development is part of Chemistry, Manufacturing and Control (CMC) Development and we are organised in R&D. We are responsible for developing formulations and production processes for soluble and freeze dried injectables of new diabetes as well as biopharm products. The department has approximately 60 employees in total and is located in Måløv.

The position
We offer you a temporary position, where you will join our projects with responsibility for product and process development to secure optimal pharmaceutical characteristics and stability. The development projects in the department include all injectables comprising GLP-1 products, insulins, haemophilia products, monoclonal antibodies and growth hormones.

Your daily work will be in close collaboration with a project team and you will for example design, interpret and report studies on drug product, write reports for internal and external use including clinical trial documentation and marketing authorisation applications. You will interact with a wide variety of internal stakeholders, e.g. Production (Product Supply), Regulatory affairs, Quality Assurance, Analytical Development, Production Pilot Plant and Discovery. Together with your colleagues you contribute to the on-going optimisation of processes and systems with LEAN as the guiding light.

You hold a Master of Science possibly combined with a PhD in Chemical Engineering, Pharmacy or another relevant scientific discipline. It is an advantage if you have working experience within drug product development, but it is not a requirement. You have strong communication skills both verbally and written in English and it is an advantage if you are able to handle spoken and written Danish.

As a person you possess drive and a positive mind-set, you enjoy working in a team with highly motivated people dedicated to developing the next generation of pharmaceuticals.

You have excellent collaborative skills and you act flexible in cooperation within the department and with stakeholders. Furthermore you work systematically and are capable of adhering to strict documentation and quality standards. Finally it is an advantage if you have leadership or project management skills.

Working at Novo Nordisk
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management and growth hormone therapy, we offer our employees opportunities for continuous growth.

For further information, please contact Ken Flemming Hansen at +45 3079 8240.

30 April 2018.

Applications will be reviewed on a rolling basis.

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