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Validation Analyst I

Kansas City, MO, US💼 Full-time🗓 2026-09-24 → 2026-09-25

Core

Support validation and qualification programs across manufacturing and laboratory disciplines to ensure compliance with guidelines and regulatory requirements.

Role type

Validation Analyst I

Builds

Validation deliverables for site-level technology rollouts, equipment/instrumentation qualification, and laboratory software/instrument implementation.

Domain

Pharmaceutical manufacturing and analytical laboratory testing

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

validation program management, GMP compliance, regulatory standards knowledge (FDA, MHRA), project management, technical writing, Microsoft Office proficiency, Six Sigma principles, change management, deviation handling, SOP development

Preferred skills

current GMP environment experience

Responsibilities

Execute validation protocols for equipment and instrumentation; collaborate with vendors and internal teams on validation deliverables; apply project management skills for software and instrument implementation; assist in developing validation policies and procedures; participate in continuous improvement initiatives.

Seniority

Mid-level, hands-on IC

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