"I have always found them to be a very professional, reliable and trustworthy organization"
Contractor, Senior Quality Associate III, Biogen
Newly built Biopharmaceutical manufacturing facility has a contract requirement for an experienced Lab Validation Engineer to generate, review & approve the IOPQ protocols and validation documents
Republic of Ireland
QA Validation Consultant Technical Writer Ireland is a hive of activity for the Life Sciences Industry at present with no shortage of major expansion/ new build facilities. We have an exciting
QAV Specialist required for a world Leading bio tech organisation who are at a peak phase in establishing an innovative and industry leading manufacturing facility in Dublin, Ireland, just 20 minutes
Do you relish the opportunity to work with a leading UK based Biologics manufacturer? If yes, then this is the assignment for you! Our biotech client with manufacturing facilities just outside
Lead CSA Engineer - France - 12-month contract initially I am currently recruiting for a Lead CSA Engineer to work for our client based in the Paris area on their Cell and Gene Therapy project