We're looking for a Validation specialist for our existing consulting company specialising in engineering and validation services for the pharmaceutical and biotechnology sectors is seeking an experienced Validation Specialist to support client projects across Italy. This role requires an onsite presence and offers the opportunity to work on complex, high value projects within regulated GMP environments.ResponsibilitiesDraft and execute qualification and validation protocols including IQ, OQ and PQPerform instrument calibration and verification activitiesPrepare and review technical documentation such as URS, VMP, Risk Assessments, GAP Analysis and P and IDLead and support qualification of HVAC systems and cleanroom environmentsExecute validation activities for critical utilities including Purified Water, Water for Injection and Clean SteamConduct qualification of process equipment including RABS, isolators, autoclaves and freeze dryersCoordinate with clients, suppliers and multidisciplinary project teams to ensure successful project deliveryMaintain compliance with GMP standards and regulatory requirementsRequirementsDemonstrated experience as a Validation Specialist within the pharmaceutical or biotechnology industryStrong knowledge of GMP regulations, ideally with exposure to EU GMP and or FDA guidelinesHands on experience with equipment, utilities and process validationAbility to manage documentation in a structured and compliant mannerStrong communication skills with the ability to work effectively across teams and stakeholdersFluent English is required. Italian would be advantageousOfferOpportunity to join a well established consultancy delivering projects across the pharma and biotech sectorOnsite work with leading clients in regulated environmentsExposure to international and technically challenging projectsCompetitive salary and benefits package based on experience#J-18808-Ljbffr