Quality Engineer

Position Summary

Phillips‑Medisize, a Molex company, is seeking a Quality Engineer at our Magnesium Molding Facility located in Eau Claire, Wisconsin. This role will champion manufacturing excellence through robust quality systems, continuous improvement, and compliance with customer and regulatory standards. This role requires strong analytical skills, cross‑functional collaboration, and a proactive mindset to integrate quality throughout product development and manufacturing.

• Interpret and negotiate customer requirements to ensure compliance with applicable standards.
• Monitor and analyze quality performance indicators; implement corrective actions to meet targets.
• Investigate daily process issues to reduce scrap and improve production yield.
• Evaluate and disposition non‑conforming parts from manufacturing, inspection, customer feedback, and returns.
• Manage supplier quality, ensuring compliance with incoming material standards and Molex supplier management policies.
• Lead customer complaint resolution using a structured approach, including root cause analysis, corrective and preventive actions, and completion of 8D and medical reporting requirements.
• Apply Advanced Quality Planning (AQP) during early product development or production transfer phases to ensure robust quality integration.
• Develop and execute validation plans (IQ/OQ/PQ) for new product introduction projects covering process, equipment, and product.
• Ensure effective implementation and management of quality control plans and manufacturing process controls, including the creation, review, and maintenance of essential quality documentation such as work instructions, inspection plans, and control plans.
• Support change management, deviations, and nonconformance handling to maintain compliance with the quality management system and customer requirements.
• Initiate and contribute to Continuous Improvement Projects aligned with plant KPIs.
• Perform other duties as assigned.

• B.S. degree in engineering or related field, or 2+ years in quality or regulatory work.
• Advanced knowledge of quality tools such as SPC, DOE, FMEA, CAPA, and root cause analysis.
• Thorough knowledge of GD&T, technical drawings and metrology.
• Corrective Actions with systemic 8D and/or medical standard approach.

• Advanced decision making and prioritization skills.
• Data analysis and project management skills.
• Effective and professional written, verbal and interpersonal communication skills.
• Extended travel to other facilities or customer locations may be required to support business needs, with travel potentially reaching up to 10 %.

Our goal is for each employee, and their families, to live fulfilling and healthy lives. We provide essential resources and support to build and maintain physical, financial, and emotional strength – focusing on overall wellbeing so you can focus on what matters most. Our benefits plan includes medical, dental, vision, flexible spending and health savings accounts, life insurance, AD&D, disability, retirement, paid vacation/time off, educational assistance, and may also include infertility assistance, paid parental leave and adoption assistance.

Specific eligibility criteria is set by the applicable Summary Plan Description, policy or guideline and benefits may vary by geographic region.

Equal Opportunity Employer, including disability and protected veteran status. Except where prohibited by state law, all offers of employment are conditioned upon successfully passing a drug test. This employer uses E‑Verify.