5+ years of QC laboratory experience, ideally including microbiology workflows
Strong understanding of QC laboratory operations and analytical workflows
Hands-on expertise with laboratory automation, particularly OneLab
Experience with LabX and/or laboratory software administration is highly desirable
Strong knowledge of GxP, CSV, data integrity, and regulated computerized systems
Experience developing validation documentation and executing UAT
Experience managing multi-site laboratory system implementation projects
Knowledge of Power BI and dashboard/report development
Experience with ALM, JIRA, Confluence, or similar information/project management tools
Excellent stakeholder management and communication skills
Ability to work effectively with international teams and manage competing priorities
Strong analytical, problem-solving, and project management capabilities
Professional working proficiency in English
You'll play a key role in the digital transformation and automation of integral QC laboratories, helping to standardize processes, improve efficiency, strengthen data integrity, and ensure compliant laboratory operations.
📌 Qc Csv Consultant – Spain (Madrid)
🏢 Digital Links
📍 Madrid
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