PERMANENT | FULL-TIME | HYBRID OR REMOTE OPTIONS AVAILABLE

Are you looking to take the lead in shaping quality and validation across a growing, international organization?
Do you bring a strong understanding of compliance and system validation in regulated environments?
Ready for your next leadership role where your expertise will drive consistency, improvement, and impact?
At Cerba Research, we are committed to finding the best talent to join our team. We have partnered with Vector Talent to manage the recruitment process for this role. If you’re interested in applying, please direct all applications and questions to Vector Talent.
Our QA team is hiring. We’re looking for a QA Computer System Validation (CSV) Manager to provide oversight and support for Cerba Research computerized systems to ensure compliance with regulatory expectations and company CSV, System Development Lifecycle (SDLC), Cybersecurity, and Data Integrity requirements.
This is a key position within a transforming QA function, as we integrate new companies and sites across the Cerba Research group. You’ll lead a small but highly experienced CSV QA team, with direct influence over validation strategy, lifecycle documentation, and system compliance across multiple GxP environments.

• Provide independent quality review and approval of system lifecycle validation documentation, such as plans, user requirements specifications, risk assessments, configuration documentation, protocols, and reports.
• Quality review and approval of IT and automation system changes and periodic review status.
• Ensure a consistent approach to qualification, change, and deviation management across systems.
• Assist in driving validation project completion in conjunction with relevant stakeholders ensuring timelines are met and deliverables achieved, ensuring when appropriate that quality by design principles are incorporated into all validation design activities.
• Support and approval of computerized systems investigations and deviations.
• Participate in audits (internal and external) where required as quality specialist and/or SME.
• Compliance with the Cerba Research Policies, Standard Operating Procedures, Work Instructions and other procedural documents relevant to the role