Title:

Senior Supplier Quality Engineer Location:

El Paso, TX Description:

Must Have Technical/Functional Skills Senior Supplier Quality Engineer will support key projects and activities with Critical suppliers in commodities such as Injection Molding, Subassemblies, plastic and other mechanical and electronic components, these activities may include set up acceptance activities, supplier audits, process validations, quality agreements negotiations, Supplier CAPAs as well as Supplier Change Requests (SCR) evaluations and dispositions Strong hands on experience in supplier qualification, approval, and lifecycle management. Proven capability to create, manage, and maintain Approved Supplier Lists (ASL). Experience conducting supplier quality system audits (on site / remote / desktop). Hands on experience leading or reviewing PPAP submissions for medical device components. Working knowledge of process validation requirements (IQ / OQ / PQ) for supplier processes. Strong understanding of risk based decision making aligned with

ISO 14971

principles. Strong skills in root cause analysis and problem solving methodologies Familiarity with electronic

QMS / PLM

systems (e.g., TrackWise, Agile, Windchill, SAP). Ability to work effectively with Procurement, Engineering, Manufacturing, QA, and Regulatory Affairs. Strong supplier communication skills (technical discussions, expectations, escalation). Ability to manage multiple suppliers and PPAPs simultaneously in a regulated environment. Ensures that suppliers deliver quality parts, materials, and services. Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur through the Supplier CAPA process. Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation. Some individuals may have responsibilities that include Pre-Market Supplier Quality and duties may include: Provides Pre-Market Quality Engineering support to New Product Development (NPD) working in partnership with the Component Engineering, Post-Market Supplier Quality and Distribution Teams, to deliver quality parts, materials, and services, prevent defects, and allow MiniMed to provide customers with the highest quality and reliable products. Define Receiving Inspection requirements as required and associated test method validation Roles & Responsibilities Main tain and update the Approved Supplier List (ASL), including supplier addition, re approval, suspension, or disqualification. Conduct supplier evaluations including quality system assessments, technical capability reviews, and regulatory compliance checks. Ensure compliance with

ISO 13485, FDA 21 CFR

Part 820, and Supplier Quality requirements. Collaborate with Procurement and Operations to ensure only ASL approved suppliers are used for sourcing and production. Define PPAP scope and level based on component risk, regulatory impact, and supplier maturity. Act as the PPAP focal point for suppliers, ensuring timely and complete submission of PPAP packages. Ensure process validations (IQ/OQ/PQ) are completed when applicable for critical or special processes. Evaluate Supplier Change Requests (SCRs) for quality, regulatory, and risk impact Participate in root cause analysis, CAPA activities, and continuous improvement initiatives as required. Support readiness for internal, customer, and regulatory audits. Collaborate with Manufacturing, Engineering, and Supplier Quality teams to resolve quality issues in a timely manner

Thanks, Saikamal Email: