CareerPlan

Quality Systems Engineer III

Indianapolis US-IN, United States | N/AFull-time2026-08-05 → 2026-10-21
HybridNo visa sponsorship

Core

Develop, establish, and maintain quality engineering methodologies, systems, and practices to meet regulatory and customer requirements while supporting new product development and manufacturing operations.

Role type

Quality Systems Engineer

Builds

Quality systems, process controls, and compliance frameworks for medical device manufacturing

Domain

Medical Devices / Quality Engineering

Required skills

Quality engineering methodologies, regulatory compliance, process control systems, CAPA management, systematic problem-solving, data analysis, cross-functional collaboration

Responsibilities

Develop and maintain quality engineering methodologies and systems; Serve as quality representative to promote quality initiatives across teams; Identify and implement effective process control systems; Lead implementation of quality assurance activities and CAPA systems; Partner with cross-functional teams to support quality disciplines throughout the product life cycle; Apply systematic problem-solving methodologies to resolve quality issues; Support continuous improvement initiatives; Organize and present quality data to influence decision-making; Maintain compliance with quality policy and procedures.