Experienced Scientists for Injectable Formulation Development in R&D

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Måløv

  • Research
  • Måløv

Are you eager to join a department linking research and production with focus on the development and documentation of formulations and processes for new injectable products? If yes, we have currently two exciting vacancies, one in early phase development and one in late phase development.

About the department

Injectable Formulation Development is part of CMC (Chemical, Manufacturing and Control) Development in the Research & Development organization. We are responsible for developing formulations and production processes for liquid and freeze-dried injectables comprising e.g. GLP-1 products, insulins, haemophilia products, monoclonal antibodies and growth hormones, and you will have ample opportunities to be part of an innovative and interesting future. The department has approximately 65 employees in total and is located in Måløv (Denmark).

In Injectable Formulation Development we develop drug product candidates for non-clinical studies and phase 1-3 clinical trials. We develop and formulate all new protein and peptide processes coming out of our research units, ensuring that we bring best-in-class treatments to the market. Working in CMC Development, you’ll be part of a team of the best and brightest in your field, where scientific integrity is standard and shared responsibility is taken for granted.

The job

As a Scientist within Injectable Formulation Development, you get to play a key role in developing the process and documentation of drug products for next generation of innovative injectables and securing optimal pharmaceutical characteristics and stability. The position in early phase development is primarily focused on drug product activities supporting non-clinical studies and phase 1 and 2 clinical trials, whereas the position in late phase development is directed towards phase 3 activities and documentation related to marked authorization applications.

You work in close collaboration with a project team and you are responsible for product and process development of new injectable drugs. In particular you:

  • design, interpret and report studies on drug products.
  • play a leading role in solving scientific and technical challenges.
  • write reports for internal and external use including clinical trial applications and marketing authorisation applications.
  • contribute to the on-going optimisation of processes and systems with LEAN as the guiding principle especially in late phase development.

This position offers you a high level of independence and flexibility within the research project work and you get the opportunity to interact with a wide variety of internal stakeholders, e.g. Global Research, Production (Product Supply), Regulatory affairs, API Development, Quality Assurance, Analytical Development, Production Pilot Plant and Clinical Supply.

Qualifications

You hold a PhD or a M.Sc. within Pharmacy, Chemistry, Biophysics, Engineering or related field of study. Ideally, you have minimum 3-5 years of experience within drug product development e.g. within formulation and/or process development, documentation, regulatory and quality aspects of drug development projects. Alternatively, you have gained relevant experience via a PhD or post-doc within pharmaceutical development or similar.

As a person, you enjoy working in a dynamic environment, where teamwork and cross-functional collaboration is on the top of the agenda. You value knowledge-sharing and you are keen to inspire your colleagues with your positive and can-do attitude. You also enjoy taking responsibility to drive your own tasks and taking initiatives to contribute to continuous improvements. Lastly, you master both verbal and written English and it is an advantage if you also master Danish or another Scandinavian language.

Contact

For further information, please contact Mette Willer at +45 3075 1662 or Anne Mette Beier at +45 3079 8535.

Deadline

12th of February 2020. Applications will be reviewed on an ongoing basis.

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 24.1.2020, men kan have været deaktiveret og genaktiveret igen.

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Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Forsker
  • Måløv
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