The Supplier Quality Engineer will be responsible for supplier related audits, evaluations, tooling, testing methods, PPAP design, and administration as it relates to the supplier by supporting current manufacturing and business growth and is proven to be vital to the success of our company.

Thorough knowledge of quality tools such as Statistical Process Control (SPC), Control Plans, Failure Mode Effects Analysis, MSA, Design of Experiments etc. Supports the suppliers on quality activities such as Control Plan, FMEA (failure mode & effects analysis), Process Capability Study, MSA (measurement system analysis), and Checklist, etc.

MANUFACTURING SUPPLIER QUALITY ENGINEER Columbus, OH PAY: $65K - $95K COMMENSURATE WITH EXPERIENCE VISA SPONSORSHIP: NO RELOCATION ASSISTANCE: YES REMOTE: NO Do you enjoy working in a fast-paced environment and being challenged.

Job DescriptionKey Responsibilities: Measurement system analysis (including but not limited to Gage R&R)Supplier ISIR (initial sample inspection report) and PPAP (production part approval process)Gage improvement projectsSupplier engagement for gage improvement and product capability improvementProblem investigation for root cause (include use of drawings, material specs, etc.

The Shelly Company, a CRH company, is a vertically integrated supplier of aggregates, asphalt, ready mix concrete and paving services throughout the state of Ohio. Our commitment to quality drives us to use the most modern, efficient and environmentally friendly technology in our industry.

Responsible for SQF readiness, Co-Packer, and Supplier quality communication. Develop and partner with Sr. QA Manager on the implementation of Safe Quality Food (SQF) programs – including HACCP, Food Safety, Food Quality and Food Defense plans.

The Supplier Quality Engineer will be responsible for executing various supplier quality engineering related activities such as Compliance, Process, and Product Audits, MRB, FAI Witnessing, Review and Sign off, Problem Solving, Corrective and Preventive Actions, Supplier Performance Reporting and other Quality Improvement Activities.

Develop, lead, direct, update, reassessment, verification and periodic validation of FSQA programs including HACCP Program, Sanitation Standard Operating Procedures, Pest Control, Good Manufacturing Practices, Approved Supplier Program, Foreign Material Control, Plant Sanitation, Chemical Control, Product Quality Assurance, FSQA Customer Complaints, Food Defense and Security.

Knowledge of security incident and event management, log analysis, network traffic analysis, malware investigation/remediation, SIEM correlation logic, and alert generation.

Supports the Supplier Quality Manager in new supplier component release/Supplier selection process for sustaining and new products. Ensures that the supplier-related risks - cost, quality, and delivery are controlled and mitigated.

Job ID: 498110 Preferred Materials - Concrete Division, part of CRH South Division, is a leading supplier of ready mix concrete, concrete block, rebar and building materials in the state of Florida, providing the highest product quality and service in the construction industry.

As The Supplier Quality Engineer, you will play a fundamental role in the scouting, benchmarking, and sourcing for suppliers that support CNH's future. NA Supplier Quality Engineer - Precision Technology.

Ensures required quality procedures are established including CAPA, Non-Conforming Product, Risk Management, Post-market-surveillance, Purchasing Controls, Management Review, Traceability, Employee Controls, Post market management, Change Control, Advisory Notifications, Supplier compliance and others as coordinated within the Quality team and with other cross-functional departments.

Previous experience working as Commodity Manager or Supplier Quality Engineer. Leveraging a nearly 75-year legacy of innovation, our ultra–high-purity products help enable high-quality processing and production for a wide range of applications in the semiconductor, photovoltaic, lighting, aerospace, water purification, pharmaceutical, consumer electronics and telecommunications industries.

This position indirectly supports ongoing manufacture of biological clinical trial materials by providing timely and compliant support for quality systems including Change Control administration, Calibration / Validation review, MasterControl system administration and workflow development, inspection management and hosting, internal auditing, supplier management, site Quality Council, quality metrics generation, and site-level compliance deliverables.