Computer System Validation

Veritaz AB

Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry. Assignment Description We are looking for an experienced Validation Lead What You Will Work On Define and lead the overall validation strategy for the project Develop verification and qualification approaches for technical systems and equipment Lead validation activities across project phases Perform and coordinate risk assessments related to validation Ensure full compliance with GMP and GxP regulations Lead Computerized System Validation (CSV) activities Validate computerized systems, manufacturing processes, and technical equipment Support validation of DeltaV or similar automation platforms Develop and maintain traceability matrices Coordinate qualification activities including IQ, OQ, and related verification processes Manage validation documentation and compliance deliverables Lead deviation investigations, CAPA activities, and corrective actions Collaborate with automation, process, commissioning, engineering, and quality teams Coordinate validation activities across multiple stakeholders Ensure successful delivery of validation objectives within project timelines What You Bring Several years of validation experience within the pharmaceutical industry Strong knowledge of GMP and GxP regulatory requirements Extensive experience with Computerized System Validation (CSV) Experience validating computerized systems, manufacturing processes, and technical equipment Practical experience with DeltaV or similar automation platforms in regulated environments Experience developing validation strategies and verification approaches Experience conducting risk assessments and qualification planning Experience with traceability matrices and requirements management Experience handling deviations, CAPA, and validation documentation Strong leadership, coordination, and stakeholder management skills Excellent communication and technical documentation skills