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MDR Scientist




I have a great new opportunity with a global company for a Medical Device Regulations Scientist.  I’m looking for someone with Medical Device experience and knowledge of Medical Device regulations, product registrations and Medical Device shelf-life.

My client is a major global pharmaceutical company.  They have a diverse business and product portfolio and an excellent reputation for the quality of their products, their employer brand and the ethics of their organisation.

The role’s responsibilities would include writing technical justifications for the stability programmes for Medical Device Regulations, writing protocols and reports for shelf-life aging studies and managing the set up of stability trials.


  • Science related degree
  • Experience in Medical Devices is essential
  • Knowledge of Medical Device stability requirements
  • Project management experience
  • Technical writing skills

To learn more about this role, please apply or contact James directly on

How to apply

If this position is of interest please send us your CV here, or you can call James Copley direct on to discuss this and other vacancies that may suit.

James Copley