Quality Engineer, High-Reliability Medical + Defense Manufacturing (ISO 9001, PPAP, Full QMS Scope)

Job Description

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This equipment powers medical devices, robotics, and defense systems. The customer list is why the quality bar is high, and why this seat carries real weight.

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Pave Talent is hiring on behalf of our client, a growing US manufacturer of high-reliability power and energy products for medical, robotics, industrial, and defense applications. Their US production site is newer and expanding, and quality is scaling with it.

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- Quality engineers who want the whole toolkit, from launch documentation to supplier corrective actions, not one narrow lane

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- People who like the production floor: training operators, auditing lines, chasing root cause where the work happens

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- Organized self-starters who keep their footing when priorities shift daily

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If you prefer a specialized lane inside a large quality department, this is not your role.

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You'll report to the Quality Manager and work side by side with the production team as the hands-on quality engineer for the site. The breadth is the draw: one role touching new product launches, supplier quality, investigations, audits, and nonconforming material decisions. That range builds a senior quality engineer's resume faster than a specialized seat.

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- Write and maintain work instructions, standard operating procedures (SOPs), control plans, and process failure mode and effects analyses (PFMEAs), and train production teams on them

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- Drive the production part approval process (PPAP) for new product introductions, from documentation through validation and approval

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- Lead root cause investigations using 8D, fishbone diagrams, 5 Whys, and Pareto analysis, and close out corrective actions

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- Manage supplier quality through supplier corrective action requests (SCARs): detailed defect reports, root cause follow-through, and verification

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- Develop and run incoming inspection, calibration, line validations, and process audits against International Organization for Standardization (ISO) 9001

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- Lead material review board (MRB) review and disposition of nonconforming product

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- Turn quality data into clear metrics and recommendations for management, primarily in Excel with pivot tables and charts

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- 2 to 4 years of quality experience in a manufacturing environment

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- Hands-on measurement and visual inspection skills

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- Statistical data analysis in Excel, including pivot tables and charts

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- Working knowledge of ISO 9001 standards and practices

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- Organized, detail-driven, and steady under deadlines

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- Validation knowledge for installation, operational, and performance qualification (IQ, OQ, PQ)

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- ISO 9001 auditing experience or auditor certification

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- Background in battery or energy storage manufacturing

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: $90,000 to $100,000, placed by experience

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: Full-time, on-site

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: Full details shared on our first call

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Interested? Apply via LinkedIn and we'll be in touch. Confidential search; your application is fully private.

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