Process Validation Engineer
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Contract: Full-time Contract
Duration: Initial 12 months (extension likely)
Start: ASAP
Location: Near Milan, Italy
Project 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 Responsibilities
* Execute Process Validation activities in line with GMP requirements
* Draft and review validation protocols and reports
* Support continued process verification (CPV) activities
* Coordinate with Production, Engineering, and Quality teams
* Monitor validation timelines and ensure documentation accuracy
* Support concurrent product validation projects
Requirements
* 3–5 years of experience in pharmaceutical xjrgpwk or regulated manufacturing environments
* Strong hands-on experience in Process Validation
* Proven experience writing and executing validation protocols
* Solid understanding of GMP regulations
* Execution-focused profile (not SME/strategy level)
* Strong on-site presence required
If this opportunity aligns with your background, please send your CV to and I will contact you to discuss next steps.