Job description

You will join our team as a QA-CSV Specialist, providing independent quality oversight and practical CSV support for execution systems used in GxP manufacturing. In this role, you will collaborate with Execution Systems, Automation, Engineering, IT, system owners, and business representatives to ensure that validation activities and lifecycle decisions remain risk-based, traceable, and inspection-ready.

Your missions

• Provide QA-CSV support throughout the system lifecycle, including projects, changes, operation, periodic review, and retirement
• Review and approve validation deliverables such as impact and compliance assessments, validation plans, requirements, risk assessments, specifications, test documentation, traceability, and summary reports
• Assess changes, incidents, deviations, defects, and CAPAs for impact on product quality, patient safety, data integrity, and the validated state
• Apply and promote a pragmatic, risk-based validation approach focused on critical functions, data, interfaces, and controls
• Assess data integrity controls for access management, audit trails, electronic records and signatures, time synchronization, backup, restore, retention, and data transfer
• Support data-flow mapping and clarify system boundaries, interfaces, critical records, metadata, and control ownership
• Support periodic reviews, inspection readiness, and audit or inspection questions for assigned systems
• Communicate quality risks clearly, challenge constructively, and escalate material compliance concerns when required

Your profile

• Experience in CSV, validation, quality assurance, automation, or computerized systems within a GxP-regulated environment (typically 4-7 years)
• Practical experience with lifecycle documentation, testing, change control, deviation management, and maintenance of the validated state
• Experience with manufacturing, monitoring, automation, or infrastructure-related computerized systems
• Good working knowledge of CSV, SDLC, EU GMP Annex 11, US FDA 21 CFR Part 11, GAMP 5, and recognized data integrity expectations, including PIC/S guidance
• Understanding of risk-based validation, electronic records and signatures, access controls, audit trails, backup and restore, interfaces, and supplier documentation
• Ability to understand technical system architecture and translate it into clear validation and quality decisions
• Effective communication, collaboration, and organization skills, with the confidence to challenge while maintaining a solution-oriented approach
• English and Dutch fluent.

Preferred experience

• PLC/SCADA, industrial automation networks, shop-floor systems, or particle monitoring solutions
• Active Directory, group policies, SIMATIC Logon, patching, antivirus, backup and restore, monitoring, or file-transfer services
• Data-flow mapping, data integrity risk assessments, periodic reviews, or inspection support

What we offer

Joining Amaris isn’t about joining a company where you simply wait patiently for a vacancy to arise. It’s about becoming part of an environment where your performance directly drives your career progression.

In practical terms, here’s what this means for you on a daily basis:

🎯 Projects worth your time 18+ months on average, with major accounts (Orange, Sanofi, SNCF, CMA-CGM…) and the support of our internal Centers of Excellence. You get the depth, not just the breadth.

🤝 Real management support 1 manager for up to 18 consultants, structured project check-ins, and a direct line to HR every month through Express Yourself. Our teams average 3.3 years of tenure — proof that we build something that lasts.

🚀 A career that actually moves 70% of our managers started at entry level. A