Quality Engineer II

Job Purpose:

Support and maintain compliance of the medical device Quality Management System (QMS), strategic quality initiatives, and cross-functional quality projects. Drive continuous improvement in product quality, regulatory compliance, and risk management across the product lifecycle. Maintain a strong working knowledge of core QMS elements, applicable standards, customer requirements, and global regulatory expectations.

• Assist or lead large‑scale or cross‑functional quality projects involving product lifecycle management, validation, CAPA, audit readiness, risk management, or supplier quality improvement.
• Serve as the Quality lead for assigned customer accounts and product groups, including support for customer complaints, nonconformances, CAPAs, customer communications, external audits, and related quality activities.
• Responsible for supporting sterilization and environmental monitoring systems, including routine sterilization validations, dose audits, and related documentation.
• Act as a quality engineering representative on new product development or design transfer projects, ensuring compliance with design control and risk management requirements.
• Develop and implement risk management strategies in accordance with ISO 14971 and maintain risk files throughout product lifecycle.
• Provide input on process validation and sterilization validation strategies, including complex or novel technologies.
• Perform, schedule, and support internal, supplier, customer, and regulatory audits, and actively support external audits, including FDA, ISO, MDSAP.
• Drive standardization and continuous improvement in QMS elements such as CAPA, complaint handling, supplier management, metrology, calibration and document control.
• Use statistical tools (SPC, DOE, MSA, QC Calc) and Lean Six Sigma methodologies to identify trends, reduce defects and improve product quality and process stability.
• Prepare, review, and approve technical documentation, including engineering change orders, validation protocols and reports, inspection plans, risk assessments, investigation reports, and other quality records as required.
• Actively participate in Value Stream Teams as a functional Quality representative, supporting first‑pass yield improvement, scrap reduction, customer complaint reduction, process improvement and overall product quality performance.
• Support customer complaint and nonconformance investigations, including data collection, root cause analysis, corrective and preventive action planning, implementation, effectiveness verification and timely closure.
• Support quality engineering activities, including Measurement System Analysis, Test Method Validation, process validation, IQ/OQ/PQ execution, inspection method development and cross‑functional project deliverables.
• Program, operate, and support vision‑based measurement systems such as Micro Vu, Keyence, or equivalent systems to establish accurate, efficient and repeatable measurement processes.
• Maintain a strong understanding of assigned customer product lines, manufacturing processes, inspection requirements and quality risks to help minimize scrap, defects and customer complaints.
• Stay abreast of changes in regulatory requirements and lead implementation of necessary updates to the QMS.
• Perform all other duties as assigned.
• Uphold SPG and Dupont vision and core values.

• Regulatory & Industry Leadership – Good understanding and knowledge of FDA, ISO, EU MDR, and MDSAP requirements. Acts as an internal authority and resource.
• Strategic Problem Solving – Leads complex problem‑solving initiatives using advanced tools (8D, DMAIC, FMEA, DOE).
• Systems Thinking – Understands how individual QMS elements connect; capable of driving systemic improvements across the organization.
• Cross‑functional Influence – Demonstrated ability to influence without authority and lead diverse teams toward quality goals.
• Mentorship & Coaching – Provides technical and professional development to less experienced engineers and team members.
• Audit Readiness & Response – Leads internal audits and prepares organization for external audits (FDA, Notified Body, customers).
• Innovation & Continuous Improvement – Drives proactive improvements to products, processes, and systems using Lean and Six Sigma methodologies.
• Risk‑Based Decision Making – Makes quality decisions by weighing compliance, business impact and patient safety.