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