Sr Quality Engineer – Medical Device

Sr Quality Engineer – Medical Device

Location: Tempe, AZ | Fully Onsite

Type: W2 contract | Duration: 12 months.

We are seeking a Senior Quality Engineer to support process development, manufacturing quality, and compliance for implantable cardiac and neuromodulation medical devices. This role focuses on inspection optimization, process and test method validation, and continuous improvement within a regulated medical device manufacturing environment.

• Lead Inspection Optimization projects (manual, automated, and semi-automated inspection)
• Support equipment development, IQ/OQ/PQ, process characterization, and validation
• Develop and execute Test Method Validation (TMV), including Gage R&R / MSA
• Ensure compliance with FDA, ISO, and GMP quality requirements
• Support CAPA, nonconformance investigations, change control, and risk management (pFMEA/dFMEA)
• Drive quality metrics, scorecards, and continuous improvement initiatives
• Collaborate cross‑functionally with manufacturing, process, and design teams.

• Bachelor’s degree in Engineering with 4+ years’ experience (or Master’s with 2+ years)
• Strong experience in medical device manufacturing quality
• Hands‑on knowledge of IQ/OQ/PQ, TMV, DOE, SPC, and statistical analysis
• Expertise in structured problem solving (DMAIC, 8D, Ishikawa)
• Excellent technical documentation and communication skills
• Proficiency with Microsoft Office tools.

• Experience in microelectronics/electronics manufacturing (SMT, wafer, IC assembly)
• Experience supporting FDA, MDSAP, or TUV audits.

Seniority level: Mid‑Senior level

Employment type: Contract

Job function: Engineering, Manufacturing, and Education

Industries: Medical Equipment Manufacturing, Medical Practices, and Engineering Services