Digital Lab Systems Specialist (LIMS, GMP) – Hybrid

Panda International; Leiden; Hybrid; EUR 70,000 - 90,000; Full time

Benefits offered by this job

Hybrid work environment

Job summary

Panda International is seeking a Senior Digital Lab IT specialist to support deployment, maintenance, and harmonization of digital laboratory systems in a GMP-regulated Advanced Therapies QC environment. You will convert paper-based lab methods into digital workflows, create and maintain method templates in LIMS, and ensure cross-site alignment with digital lab standards.

The role requires 5+ years in Quality Control/Quality Assurance, IT, or Laboratory Operations, plus strong communication and

Qualifications

• Bachelor's degree in a chemical, life sciences or relevant technical discipline.
• 5+ years of experience in QC/QA, analytical testing, IT, or laboratory operations.
• Experience in highly regulated pharmaceutical/biotech environments.
• Proven experience with digital laboratory systems and LIMS.
• Strong understanding of lab processes and digitalisation of workflows.
• Experience creating or managing digital lab methods and templates.
• Experience with master data and LIMS configuration activities.
• Strong communication and presentation skills
• Fluent English (written and spoken)

Responsibilities

• Digital method implementation and LIMS configuration across sites.
• Change-control support and technical documentation upkeep.
• Master data validation and method template maintenance.
• Operator training and troubleshooting for digital workflows.
• Support LIMS–instrument interfaces and data integrity

Skills

Quality control

Quality assurance

Analytical testing

IT

Laboratory operations

Digital lab workflows

Communication skills

Fluent English

Education

Bachelor's degree in Chemical/Life Sciences or relevant

Master's degree or advanced degree

Tools

LIMS

LabVantage LIMS

Job description

Panda International is seeking a Senior Digital Lab IT specialist to support deployment, maintenance, and harmonization of digital laboratory systems in a GMP-regulated Advanced Therapies QC environment. You will convert paper-based lab methods into digital workflows, create and maintain method templates in LIMS, and ensure cross-site alignment with digital lab standards.

The role requires 5+ years in Quality Control/Quality Assurance, IT, or Laboratory Operations, plus strong communication and