Computer System Validation (CSV) Lead 18582

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