Roles & responsibilities:Our client is looking for a Lab Vantage LIMS Admin.They are utilizing version 8.6 to support and maintain their laboratory informatics systems within a regulated GMP pharmaceutical environment.The ideal candidate will manage user support, and compliance activities to ensure reliable and efficient lab operations.They will act as the liaison between site QC and the global team.They will attend meetings at the site level and make sure they are aligned with global standards.It is a very structured job around keeping up the Elim's, keeping it up to date, working with QA if there are issues with compliance.They should have 3-5 years of GMP and understand ALCOA principles.They will administer and maintain Lab Vantage v8.6, including user roles, workflows, and master data.They will support laboratory users and troubleshoot system-related issues.This person will collaborate with QA, QC, and IT teams to ensure data integrity and GMP compliance.
