Quality Engineer II
Core
Drive product compliance, root cause analysis, and quality assurance across manufacturing operations for medical technology, defense, and industrial automation products.
Role type
Quality Engineer II (Manufacturing)
Builds
Quality management systems, validation plans, and compliance documentation for complex industrial and medical products.
Domain
Manufacturing / Medical Technology / Defense / Industrial Automation
Required skills
Root cause analysis, CAPA management, QMS audit oversight, validation planning, inspection strategy design, process documentation, cross-functional leadership, structured problem-solving, experimental design
Preferred skills
Bachelor's degree, 2+ years quality/manufacturing experience, coaching and mentoring technicians
Technologies
QMS tools, Engineering Change Order (ECO) systems, Master Validation Plans
Responsibilities
Lead non-conformance resolution and customer complaint management; Support internal and external audits; Monitor operations and execute containment/purges; Train operators on compliance procedures; Design and control repeatable manufacturing processes.
Seniority
Mid-level, hands-on IC