GMP Lab Automation Specialist — CAPA & LIMS Expert

Talentmark; Leiden; Presencial; EUR 60 000 - 90 000; Tempo integral

Resumo da oferta

Talentmark in Leiden seeks an automation specialist for pharmaceutical QC labs. You will combine hands-on programming with non-conformance investigations to strengthen data integrity and ensure GMP and 21 CFR Part 11 compliance.

You will maintain laboratory systems, from analytical instruments to LIMS-connected platforms, document technical work, and collaborate on automation projects and audits across teams.

Qualificações

• Bachelor's degree or higher in Life Sciences or related field with GMP exposure.
• Experience with GxP environments and data integrity concepts is required.
• Experience in non-conformance investigations and CAPA processes is a plus.

Responsabilidades

• Lead non-conformance investigations, identify root causes and drive CAPA.
• Implement, maintain and troubleshoot laboratory automation systems and LIMS-connected platforms.
• Safeguard data integrity, maintain technical documentation and support GMP/21 CFR Part 11 compliance.
• Collaborate across teams on automation projects, continuous improvement and audit readiness.

Conhecimentos

Automation programming

Data integrity

Analytical mindset

Formação académica

BSc HBO Life Sciences

Ferramentas

Empower

LIMS

TrackWise

Descrição da oferta de emprego

Talentmark in Leiden seeks an automation specialist for pharmaceutical QC labs. You will combine hands-on programming with non-conformance investigations to strengthen data integrity and ensure GMP and 21 CFR Part 11 compliance.

You will maintain laboratory systems, from analytical instruments to LIMS-connected platforms, document technical work, and collaborate on automation projects and audits across teams.