LabVantage LIMS Admin

• Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
• We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

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.

All your information will be kept confidential according to EEO guidelines.