This is a hands-on commissioning, qualification and validation role with high growth potential. You will work alongside our CQV Lead on facility, utility and equipment qualification programs for pharmaceutical and biotechnology clients — writing and executing protocols, working in the field, and building toward owning systems independently. We are looking for someone with real GMP experience who wants to move further into validation than their current role allows. Author and execute commissioning and qualification protocols — IQ, OQ and PQ — for utilities, equipment and facilities. Perform field verification and walkdowns against P&IDs, and log discrepancies for resolution. Execute qualification sampling programs and maintain complete, accurate records — sample logs, chain of custody and executed protocols. Write deviation reports and summary reports, and support investigations. Support risk assessments and FMEAs, and the sampling plans that follow from them. Support change control, and help close out qualification packages. Work with client engineering and quality teams on site, representing Eurofins professionally. As you grow: take ownership of systems end to end, mentor newer engineers, and lead your own qualification workstreams. 
