Start: ASAP
Project Type: Pharmaceutical / Consumer Healthcare Manufacturing
We are currently supporting a large manufacturing site near Milan experiencing increased activity driven by new product introductions and ongoing validation requirements.
As part of the site’s expansion and validation workload, we are seeking experienced Cleaning Validation Engineers to support hands‑on execution activities.
The validation systems and SMEs are already established. This role is focused on protocol writing, execution on the shop floor, and documentation support across multiple active projects.
Multiple hires are planned, with further validation projects expected throughout the year.
Key Responsibilities
* Execute Cleaning Validation activities in line with GMP requirements
* Draft and review cleaning validation protocols and reports
* Perform risk assessments and define sampling strategies
* Support swab and rinse sampling activities
* Coordinate with Production, Quality, and Engineering teams
* Ensure compliance with regulatory standards and internal procedures
Requirements
* 3–5 years of experience within pharmaceutical or regulated manufacturing environments
* Strong hands‑on experience in Cleaning Validation
* Proven experience writing and executing validation protocols
* Solid understanding of GMP requirements
* Execution-focused mindset (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.
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