Validation Specialist
Katalyst HealthCares & Life Sciences
Job Title
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
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
- Job-ID32495586Reference26-01079Remote50% RemoteResponsibilities:Lead validation activities for Labware LIMS 8 implementationAuthor and review IQ/OQ/PQ, RTM, and validation documentationEnsure compliance with GXP, CSV, and regulatory standardsSupport audits, inspections...Suggested
$29 - $49 per hour
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About Client: The client is a global technology, consulting, and digital solutions company with problem-solving abilities and an emphasis on developing ingenious solutions that allow its clients to remain competitive, profitable, and secure in an evolving business environment...$82k - $120k
Manufacturing Engineer Eaton's AER FED Fluid Electrical Distribution division is currently seeking a Manufacturing Engineer. This is a Full-Time role (Monday-Friday, Daylight) based at our manufacturing site in Camarillo, CA! The expected annual salary range for ...Permanent employmentFull timeWork at officeRelocation packageMonday to Friday- ...drive measurable improvements across the manufacturing floor. The Manufacturing Engineer is responsible for process development, validation, documentation, and sustaining engineering activities in support of existing and new products in a GMP medical device environment...Local area
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