This position is open exclusively to people who are eligible to work in USA

Overview

Seeking a Quality Engineer within the medical device industry to support quality assurance activities, compliance, and continuous improvement initiatives in a regulated environment.

Required Experience

• 3+ years of experience in Quality Engineering within medical device or regulated industry
• Strong knowledge of FDA regulations (21 CFR Part 820) and ISO 13485
• Experience with CAPA, NCR, and Root Cause Analysis
• Hands‑on experience in validation (IQ/OQ/PQ) and process improvements
• Familiarity with risk management (FMEA) and documentation control

Key Responsibilities

• Support quality systems to ensure compliance with regulatory and company standards
• Lead and participate in CAPA investigations and root cause analysis