Process Validation Engineer
Contract: Full-time ContractDuration: Initial 12 months (extension likely)Start: ASAPLocation: Near Milan, ItalyProject Type: Pharmaceutical / Consumer Healthcare Manufacturing
We are currently supporting a large manufacturing site near Milan undergoing significant product expansion and increased validation activity.Due to a strong pipeline of new product launches, there is an immediate need for experienced Process Validation Engineers to support ongoing validation execution on site.The validation framework and SMEs are already established. This role is focused on hands-on execution, protocol development, and documentation support across multiple active projects.Several hires are planned, with further project demand expected throughout the year.
Key ResponsibilitiesExecute Process Validation activities in line with GMP requirementsDraft and review validation protocols and reportsSupport continued process verification (CPV) activitiesCoordinate with Production, Engineering, and Quality teamsMonitor validation timelines and ensure documentation accuracySupport concurrent product validation projects
Requirements3–5 years of experience in pharmaceutical or regulated manufacturing environmentsStrong hands-on experience in Process ValidationProven experience writing and executing validation protocolsSolid understanding of GMP regulationsExecution-focused profile (not SME/strategy level)Strong on-site presence required
If this opportunity aligns with your background, please send your CV to ngiselle@optimussearch.com and I will contact you to discuss next steps.