KMC Systems, an Elbit Systems of America company, offers an ecosystem of engineering and innovation to develop the most advanced clinical and operational solutions for leading medical device customers across a diverse range of market segments. KMC was established in Merrimack, NH, in 1980, conveying almost half a century of innovation, R&D of next generation devices, and the agility to evolve to meet changing market dynamics. This has kept KMC at the forefront of technological advancements and as the premier choice for leading global medical device and healthcare companies. KMC is a full-suite provider with services in: Engineering Design, Manufacturing, Product Ideation, Product Lifecycle Management, and Sustaining Engineering.

We are looking for extraordinary people to join #OneTeamOneMission to create and deliver innovative solutions that protect and save lives

This is an onsite position in our Merrimack, NH facility 

The Principal Supplier Quality Engineer works on behalf of Elbit Systems of America Operations (KMC) to provide direction and oversight of KMC suppliers. Work in a team environment with suppliers to develop and implement best practices that emphasize defect prevention, reduction in variation and waste and provide for continuous improvements in meeting all customer requirements. Collect root cause analysis and provide corrective feedback to prevent line stops due to supply issues. Manage the customer-specific requirements and offer technical support to suppliers. Responsible for ensuring that the products produced meet quality standards required to minimize quality costs and maximize customer satisfaction whilst ensuring that procedures and processes are adhered to. Maintain the robustness of product builds following new product introductions to ensure continuity and improvement in supplier capability. Manage the customer-specific requirements and offer technical support. Work on multiple phases or sub-tasks of projects or entire projects of high complexity, with results impacting on project completion. He/she must demonstrate attention to detail, strong Lean Principles, analytical skills, documentation, processes, and excellent verbal / written communication.

Responsibilities 

• Perform Supplier evaluation audits, supplier support and supplier advanced quality planning (AQP).
• Manage supplier performance by monitoring of quality, delivery, and cost metrics and developing corrective action plans when appropriate.
• Review potential suppliers for acceptability to ASL
• Support the evaluation/classification of suppliers
• Work with the supplier directly to support business requirements: Non-Conforming Material Reports (NCMR’s) and Supplier Corrective Actions (SCAR’s).
• Facilitate root cause analysis and corrective actions of supplier quality issues, Identify and recommends processes, procedures, and equipment.
• Audit suppliers for root cause analysis and verification of correction actions of supplier quality issues.
• Interact with Supplier to ensure timely Non-Conforming Material Reports (NCMR’s) and Supplier Corrective Actions (SCAR’s), including effectiveness and verification.
• Work with Design and Manufacturing Engineering teams to define process parameters and criteria to ensure supplier process capability is effective to meet product and process requirements.
• Supporting complete and accurate documentation of inspection results as defined by regulations, product specifications or Control Plans, Part Approval Process or product warrant submission.
• Review supplier manufacturing processes, collaborate with suppliers on process improvement and value enhancement opportunities.
• Promote the use of preferred techniques for continuous improvement such as Lean, Poka-Yoke, Measurement System Analysis, and Process Failure Mode and Effects Analysis (PFMEA)
• Provide leadership to identification and development of suppliers with respect to technology, performance, quality, cost, logistics, and delivery through the application of professionally accepted techniques, practices and procedures 

 Competencies:

• Supplier Audit
• Quality Systems, Standards, and Methodology
• Continuous Improvement: Lean principals, 5S plus 1, P/FMEA, Visual Factory
• Problem Analysis & Solving
• Product Design & Development
• Statistical Process Control (SPC)
• Human Factors, Ergonomics and Safety
• Enterprise-wide Systems Integration (PLM, MRP, MES, ERP, etc.)
• Failure Analysis
• Engineering specifications - Schematics, Layouts, prints

• Bachelor’s Degree in an Engineering (Electrical, Mechanical) and 8 years of related experience in a manufacturing environment.
• Proficient in the above competencies and or an equivalent combination of education and experience
• Strong organizational, interpersonal, analytical, communication and presentation skills
• Lead Auditor Certification ISO 9001 and 13485
• Lean Green belt
• Innovative & Creative
• Medical Device Industry experience
• Proficient with Windows operating systems and Microsoft Office programs
• Experience with Mini-tab application plus
• Experience working with suppliers of PCBAs and other electrical components is highly preferred
• Requires daily onsite presence

#LI-SW1

#LI-ONSITE

This position will be focused on suppliers of electrical components such as PCBA's.  Previous experience and expertise working with such suppliers is needed.  

All your information will be kept confidential according to EEO guidelines.

No sponsorship will be offered for this role.