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Job description
Lead validation activities for Labware LIMS 8 implementation
Author and review IQ/OQ/PQ, RTM, and validation documentation
Ensure compliance with GXP, CSV, and regulatory standards
Support audits, inspections, and validation testing activities.
Responsibilities
Lead validation activities for Labware LIMS 8 implementation
Author and review IQ/OQ/PQ, RTM, and validation documentation
Ensure compliance with GXP, CSV, and regulatory standards
Support audits, inspections, and validation testing activities.
Required Skills:
Labware LIMS (Labware 8 Preferred)
Computer System Validation (CSV)
GXP / GMP Environment
GAMP 5 & Regulatory Compliance
IQ / OQ / PQ Documentation
Requirements Traceability Matrix (RTM)
Validation Strategy & Execution
Audit Readiness & Inspection Support
Deviation, CAPA & Change Control Management
Laboratory Systems & Enterprise GMP Systems Validation.
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Worksite address
thousand oaks, CA, 91362, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.