QA-CSV & Digitalization Site Key User (F/M/X)

MANTU GROUP SA; Beerse; Remote; EUR 70,000 - 100,000; Full time

Benefits offered by this job

Health insurance

Remote work option

Meal vouchers

Time savings account

Referral bonus

Job summary

Mantu Group SA seeks a QA-CSV Professional to provide independent oversight in a GxP environment. You will validate execution systems and act as site lead for Checklyst Manager, driving digital transformation and data integrity across the site.

The role requires 4–7 years in CSV/validation, strong documentation discipline, and ability to coordinate across multiple teams. Fluent English is required; Dutch is a plus. Hybrid work and competitive benefits are offered.

Qualifications

• Experience in CSV, validation, quality assurance, digital systems within a GxP-regulated environment (4–7 years).
• Lifecycle documentation, testing, change control, deviation management, and maintenance of the validated state.
• Experience supporting system users, coordinating stakeholders, or acting in a key-user or system-governance role.
• Knowledge of CSV, SDLC, EU GMP Annex 11, US FDA 21 CFR Part 11, GAMP 5, and data integrity expectations.

Responsibilities

• Provide QA-CSV oversight for PLC/SCADA-based automation and visualization systems.
• Review and approve validation deliverables and traceability documentation.
• Assess changes, incidents, deviations, and CAPAs for impact on quality and data integrity.
• Coordinate creation, testing, and documentation of new digital checklists in Checklyst Manager.
• Onboard new areas and ensure readiness for adoption; govern user access and provisioning.

Skills

QA-CSV

Validation

GxP

Data integrity

Digital systems

Stakeholder coordination

English fluency

Dutch language

Education

Bachelor or Master in Engineering/Automation/CS/Life Sciences

Tools

Checklyst Manager

SIMATIC Logon

Active Directory

Job description

Join our team and start a new adventure in an international and dynamic environment, where you will be able to fulfil your career expectations in a fast-growing organization.

In this combined role, you will support two complementary areas within a GxP manufacturing environment. You will provide independent QA-CSV oversight and practical validation support for execution systems, while also acting as the Site Key User for Checklyst Manager, a core digitalization system supporting the transition from paper to controlled digital checklists. This position is critical to ensuring robust quality assurance, data integrity, and digital transformation across the site.

Your missions

• Provide QA-CSV support for PLC and SCADA-based automation and visualization systems, particle and environmental monitoring systems, and automation network shared services (including Active Directory, access and policy management, backup and restore, patching, antivirus, and infrastructure monitoring).
• Review and approve validation deliverables, including assessments, 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 validated state.
• Apply a pragmatic, risk-based approach focused on critical functions, data, interfaces, and controls.
• Assess controls for access management, audit trails, electronic records and signatures, time synchronization, backup, restore, retention, and data transfer.
• Support data-flow mapping, inspection readiness, periodic reviews, and elevate material quality risks as needed.
• Coordinate and oversee the creation, configuration, testing, and documentation of new digital checklists in Checklyst Manager.
• Ensure new or changed checklists are reviewed, tested, approved, and released before operational use.
• Onboard new areas and teams, align on intended use, responsibilities, training, and readiness for adoption.
• Govern user access, support timely provisioning, modification, and removal of access, and periodically review roles and responsibilities within the system.
• Provide first-line functional guidance to users, authors, reviewers, and area representatives, and coordinate escalation of system issues.
• Run and review system and process metrics, identify overdue or non-compliant records, and coordinate follow-up actions.
• Ensure records are controlled, monitored, and closed within acceptable timelines, escalating delays as necessary.
• Support continuous improvement, standardization, and site governance.

Your profile

• Experience in CSV, validation, quality assurance, digital systems, 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 supporting system users, coordinating stakeholders, or acting in a key-user, application-support, or system-governance role
• 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 computerized-system documentation
• Experience with PLC/SCADA, industrial automation networks, particle monitoring or shared automation services
• Experience with Active Directory, SIMATIC Logon, backup and restore, data transfer or infrastructure monitoring
• Experience with digital checklist, workflow, electronic form or calculation-management solutions
• Experience with data-flow mapping, data integrity risk assessments, access governance, metrics or inspection support
• Academic background: Bachelor or Master degree in Engineering, Automation, Computer Science, Life Sciences, or a comparable technical or scientific discipline
• English fluent; Dutch is a strong plus
• You demonstrate the ability to translate business processes and paper-based activities into clear, controlled digital workflows and checklists, and to coordinate onboarding, testing, documentation, access governance, metrics, and timely record closure across multiple teams

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. Average age: 36. Here, trust comes before experience and merit drives progression — not seniority. Functional (4 areas of expertise) and geographic (60+ countries) mobility are actively encouraged.

Innovation, in practice 291 AI agents built in-house, 250+ training modules, Microsoft certifications fully funded. At Mantu, AI stands for Artificial Intelligence — and Augmented Impact.

CSR with real targets SBTi carbon reduction roadmap, 32% women in management (target: 34.3% by 2029), social engagement through We Care Together.

Health insurance, remote work, meal vouchers, time savings account, referral bonus… We’ll talk about our full benefits package during our interviews.

Mantu is proud to be an equal opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.