QbD Group · Posted 9mo ago
Data Integrity & Validation Consultant (GxP)
- Location
- 🇳🇱 Breda, Netherlands
- Contract
- Full-time
- Role
- Other data roles
- Source
- Employer’s own job board (Teamtailor)
The posting
🔍 Data Integrity & Validation Consultant (GxP)
📍 Location : Hybrid 🕓 Type : Full-time
Are you passionate about automation, analytical equipment, and data integrity in a regulated (GxP) environment ? Do you enjoy working where quality, compliance, and technology meet — and making sure systems and processes are not only working, but audit-ready and future-proof ?
We are looking for an Data Integrity & Validation Consultant (GxP) who’s ready to support life sciences companies in building strong, compliant, and reliable processes across QC and production environments. In this role, you’ll apply ALCOA+ principles , strengthen data integrity governance , and support clients during implementations, validations, audits, and inspections .
This position is ideal for someone who takes ownership, enjoys working across teams, and gets energy from solving complex quality and compliance challenges — while helping others grow along the way. If you’re ready to make an impact in the Life Sciences industry (and grow while doing it), we’d love to hear from you
💡 What’s in it for you?
Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices
Grow within a community of experts: Benefit from knowledge-sharing, mentoring, and exposure to diverse assignments that broaden your expertise in automation, data integrity, and compliance.
Build a meaningful career: As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.
A fair, competitive package: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued.
💪 What you bring
• Act as a Data Integrity (DI) specialist , monitoring and supporting compliance across QC and operational environments
• Ensure data integrity compliance during implementation of analytical equipment and automated systems
• Apply and embed ALCOA+ principles across processes, systems, and ways of working
• Bring advanced expertise on data integrity expectations, standards, and best practices within regulated environments
• Identify DI risks and issues, create and own Quality Risk Assessments , and ensure they lead to clear actions
• Review outcomes of quality audits and inspections and support the development and execution of corrective and preventive action plans (CAPA)
• Support or lead deviation management related to data integrity and compliance topics
• Consult on new testing procedures and procedural changes , ensuring DI is built in from the start
• Provide DI support during equipment validations (e.g., audit trail reviews/validation, system integrity checks)
• Support DI guidance during change control , ensuring validated and compliant status is maintained
• Deploy and own DI Gemba walks and translate observations into sustainable improvements
• Lead or support data integrity governance processes and help strengthen standard ways of working
• Support inspection readiness and collaborate in internal and external audits
• Coach, train, and guide colleagues and stakeholders to raise awareness and maturity around DI
• Work according to compliance best practices, EHSS requirements and lean principles
• Perform other work-related activities assigned by your supervisor
🫵 Who you are
Our culture is driven by values If this sounds like you, you’ll fit right in:
• You’re resilient and tackle challenges with a positive mindset
• You’re curious and always up for learning something new
• You have a no non-sense approach honest, clear, respectful
• You’re innovative and bring ideas, not just opinions
• And above all, you’re serious about your work, but not too serious about yourself
✨ About us
We support life sciences companies from idea to patient — offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and pharma.
We believe in JPEG : Joy. Partnership. Going the Extra Mile. Getting Things Done.
You won’t just be taking a job — you’ll be joining a community where people grow, laugh, build, and contribute to something bigger.
📩 Interested? Let’s talk. Send us your CV and motivation letter. You could be the next one to join the QbD family.