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 Elims 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.
Additional Information :
All your information will be kept confidential according to EEO guidelines.
Remote Work :
No
Employment Type :
Contract