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NL - Analyst 4, IT Business Rel Mgmt
Panda International B.V.
About the role
Paperless Lab – Subject Matter Expert
Responsible for supporting the deployment, maintenance, and harmonization of digital laboratory systems within a GMP-regulated Advanced Therapies QC environment. The role focuses on converting paper-based laboratory methods into digital workflows, creating and maintaining method execution templates in LIMS, supporting master data and validation activities, and ensuring alignment with digital lab standards across sites. Responsibilities include digital method implementation, LIMS configuration, change-control support, technical documentation, master data validation, operator training, troubleshooting, and supporting LIMS–instrument interfaces.
Start Date: ASAP
Contract Duration: 4 months (high possibility of extension)
Location: Leiden, Netherlands
Hours: 40 hours per week
Work Arrangement: Hybrid
Interested in discussing this opportunity or know someone who could be a great fit? Send your CV to [email protected].
What you'll bring
Bachelor's degree or equivalent in Chemical, Life Sciences, or another relevant technical discipline
5+ years of relevant experience in Quality Control, Quality Assurance, Analytical Testing, IT, or Laboratory Operations
Experience working in a pharmaceutical, biotechnology, Advanced Therapies, medical device, or other highly regulated environment
Proven experience working with digital laboratory systems and LIMS
Strong understanding of laboratory processes and digitalisation of laboratory workflows
Experience creating, updating, or managing digital laboratory methods or workflows
Experience with master data, method templates, or similar LIMS configuration activities
Strong communication and presentation skills
Fluent English (written and spoken)
Nice to have
Experience with LabVantage LIMS
Experience as a LIMS key user, business administrator, or SME
Experience connecting laboratory instruments with LIMS
Experience supporting LIMS–instrument interface setup and validation
Experience with method harmonization or standardization across sites
Experience with Change Control and validation activities in a GMP environment
Experience creating or maintaining technical documentation
Experience delivering training to laboratory operators
Experience participating in process improvement or digital transformation projects
Experience in Advanced Therapies or biologics
Master's degree or other advanced degree