Role - QC CSV Consultant
Duration - ASAP till end of the year with extensions
Location - 100% Remote in Europe
Roles & Responsibilities 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 One Lab 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 general QC laboratories, helping to standardize processes, improve efficiency, strengthen data integrity, and ensure compliant laboratory operations.

📌 Qc Csv Consultant – Spain (Málaga)
🏢 Digital Links
📍 Málaga