Lead implementation kick off activities for multiple QC laboratory systems within a GMP regulated environment
Coordinate and oversee end to end system integrations across laboratory instruments, software applications, and enterprise platforms
Manage project execution against agreed scope, timeline, budget, and quality objectives
Drive alignment between laboratory operations, IT, vendors, QA, and validation stakeholders
Monitor implementation progress, identify risks, and proactively resolve integration issues
Support data migration and system consolidation activities across legacy and target platforms
Ensure proper documentation and compliance with internal CSV / CSA and GxP requirements
Support QA and validation teams during IQ / OQ / PQ execution
Review validation deliverables, test evidence, deviations, and remediation actions
Prepare systems for compliant go live and handover to operational support teams

Strong experience in QC laboratory systems integration within GMP regulated environments
Proven track record in implementation of laboratory instruments and associated software platforms
Solid understanding of computer system validation, data integrity, and GxP compliance
Experience supporting IQ / OQ / PQ activities in collaboration with QA
Strong stakeholder management across laboratory, IT, quality, and vendor organizations
Ability to manage multiple parallel workstreams in a complex program environment
Excellent communication and coordination skills in cross functional teams
Experience in pharmaceutical, biotech, or life sciences environments (preferred)
Strong familiarity with QC laboratory workflows and analytical instruments (preferred)
Knowledge of regulated migration and system consolidation programs (preferred)

QC Systems Integration Consultant – GMP Laboratory Systems

Key skills