Administrative Skills, Artificial Intelligence (AI), Biotech and Pharmaceutical, Business Analysis, Communication Skills, Cross-Functional, Environmental Communications, GMP (Good Manufacturing Practices), Laboratory Equipment, Laboratory Information Management System (LIMS), Laboratory Operations, Labware, Materials Testing, Product Testing, Project/Program Management, Regulations, Requirements Validation/Verification, Test Lab, Time Management, Traceability
LabWare 8 LIMS Configuration & Integration Specialist
CONTRACT THRU MARCH 2027, with possible extensionLOCATION: Thousand Oaks , CA - Onsite (So under 50 miles or local only)
No H1b and CPT.
Client name will not be disclosed until after a qualified candidate resume is presented.
Note :
Two recent work references will be required from candidates UPON SUBMISSION. Resumes will be screened by an AI tool and blatant AI generated resumes will be rejected.
Update from the Hiring Manager- Strong hands-on experience with LabWare 8 configuration or technical development
- Experience in configuring Raw Material Workflows in Labware or Instrument/Equipment integration (Empower/LabX to Labware) preferred
- Experience with previous LabWare versions is not acceptable, as they differ from LabWare 8
- Not seeking candidates whose experience is limited to Business Analyst, Project Management, Administration, or Support roles
Requirements for the role:- MUST HAVE hands on experience configuring LabWare 8 LIMS
- Completed on time LabWare LIMS configurations for raw materials, commercial products, and equipment integration.
- Strong experience with Labware within GMP laboratory operations, particularly Raw materials testing, Commercial product testing and Laboratory equipment workflows
- Demonstrated ability to translate regulatory and quality requirements into compliant LIMS configurations.
- Experience supporting LIMS validation with full requirements to configuration to validation traceability.
- Experience integrating LabWare with Instrument systems (e.g., Empower, LabX)
- Experience executing stable & compliant configured workflows in operations.
- Experience working in biopharmaceutical or pharmaceutical GMP environments preferred.
- Strong cross functional communication skills in regulated environments
- Experience supporting inspection readiness activities related to LIMS
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Shiftcode Analytics, Inc