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Senior QA Specialist (Grand Rapids, MI)

Grand Rapids, MI, us💼 Full-time🗓 2026-04-30 → 2026-07-31

Core

Ensuring quality assurance compliance for pharmaceutical manufacturing from raw material inspection through final product shipment, while driving quality projects and process optimization.

Role type

Senior QA Specialist (Project Management & Compliance)

Builds

Quality projects, process improvements, and compliance initiatives for pharmaceutical manufacturing.

Domain

Pharmaceutical manufacturing / Quality Assurance

Deliverable

client delivery

Required skills

Project Management, Scheduling, Inventory Control, Data Analysis, Risk Assessment, Regulatory Compliance (GMP/GLP), Visual Management, Metrics Reporting

Preferred skills

Statistics knowledge

Technologies

Excel, Word, PowerPoint

Responsibilities

Develop and execute quality projects across multiple site QA areas; Coordinate with site QA planners and centralized functions; Analyze and maintain data to optimize QA processes; Lead development of Project Charters and define project objectives; Support Regulatory inspections for new market introduction; Lead Compliance and Performance improvement projects; Report metrics and project status to site management.

Seniority

Senior, hands-on IC

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