Excellent opportunity to work for a global life sciences company within new product development and project management.

The main responsibilities of the role will be the activities required for the development of new and novel IVD devices for use in cancer detection. They will include management of clinical trials, liaison with external evaluation sites, preparation of detailed project plans and timelines, interpretation of FDA guidelines relating to development of CLASS III IVD reagents.

Technical responsibilities will center on antibody optimization (antibody titration curves, selection of appropriate pre treatment conditions) in situ hybridization, use of automated immunostaining platforms, microscopic slide examination, data analysis, and report writing.

It is highly desirable that candidates are educated to MSc degree in molecular biology, histology or related subject. Experience of working in a research laboratory in academic and/or industry environment is essential.

A strong knowledge of regulations and standards affecting IVDs and Biologics is required.

The ideal candidate will be highly motivated, possess a strong commitment to detail, and have the capacity to remain focused throughout a complex multistage process.