Pharma Point, on behalf of a leading multinational company in the pharmaceutical equipment solutions sector, is looking for a Validation Specialist.

The role will be responsible for managing and supporting validation and qualification activities for pharmaceutical products, both in-house and at client sites, ensuring compliance with regulations and company policies.

Main Responsibilities:
Drafting and executing validation tests (FAT, SAT, IQ, OQ).
Compiling validation protocols for critical pharmaceutical machinery.
Supporting the resolution of deviations/investigations.
Preparing quality documentation for projects.
Monitoring project progress and addressing critical issues.

Requirements:
Knowledge of GMP, GAMP5, and Quality Risk Management regulations.
Experience in validation and testing processes (FAT, SAT, IQ/OQ).
Minimum B2 level English proficiency.
Flexibility and availability for travel.

Location: Varese (VA).