Job Description
Small molecules. In vitro assays, in vivo assays. Internally. Support whole of the clients portfolio. Small, large molecules and peptides. Into areas of proteomics.
Training in large molecules.
Hands on experience in proteins.
Very small and very flexible team.
Will interact with the team in Belgium.
Stakeholders across the organisation in one building and working with the chemists and pharmacology, all the wider team.
Requirements
Experience:
significant exp 3 years minimum ideally in small and large molecules in bioanalysis, hires mass spectrometry.
Small molecules is a must.
Lab automation.
Reporting software. MS office based.
Essential Skills: bioanalytical experience is key in vitro or in vivo.
Desirable skills: large molecules and peptides can be trained
Education requirements: Ba plus experience, very practical role so must have hands on industry experience
Requirements
Qualifications • 3+ years’ experience in the regulated pharmaceutical industry, with 1-2 years in QA or manufacturing. • Strong knowledge and experience with US/EU GMPs, ICH and other applicable international regulations • Experience with the production and testing of pharmaceuticals (biologic or small molecules) • Experience working with contract givers preferred • Excellent communication skills and proven ability to work well with internal and external teams • Experience with electronic documentation management systems preferred • Ability to prioritize work and handle multiple assignments, while maintaining a high level of quality • Fluency in English is a must • thorough understanding of local compliance, as well as a sound ethical approach to business Education • Minimum of Bachelor’s degree in a scientific discipline (Chemistry, Biology, etc.)