VALIDATION SPECIALIST Business unit Ingegneria e Servizi Tecnici; Quality Unit Sedi Italia/Lombardia/Varese 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 Punch Lists and managing validations. Collaborating on the drafting of technical and regulatory documents. Preparing quality documentation for projects. Monitoring project progress and addressing critical issues. Supervising external personnel and archiving documentation. 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. Result-oriented with strong attention to quality. Team-working and excellent communication skills. Customer-oriented approach with strong relationship management skills. Location: Varese (VA). Indietro Business unit Ingegneria e Servizi Tecnici; Quality Unit Sedi Italia/Lombardia/Varese