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Supplier Quality Engineer II

Job in Aurora, Kane County, Illinois, 60505, USA
Listing for: DiaSorin
Full Time position
Listed on 2026-07-19
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 69000 - 117000 USD Yearly USD 69000.00 117000.00 YEAR
Job Description & How to Apply Below

Supplier Quality Engineer II Obsessed by Science. Entrepreneurial by Nature. United by Purpose.

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide. For more than 50 years, we have combined scientific rigor with an entrepreneurial mindset, operating with a strong commitment to innovation, accountability, and results to deliver trusted diagnostic solutions.

As the Diagnostics Specialist, Diasorin continuously invests in research, technology, and people. Guided by our values of operational excellence, customer focus, and teamwork, we empower teams to think boldly, act decisively, and transform ideas into meaningful impact across one of the industry’s broadest specialty diagnostic portfolios.

When you join Diasorin, you are not just filling a role. You are helping build what comes next.

Why Join Diasorin
  • Build What Matters. Take ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide.
  • Innovate with Agility at a Global Scale. Work in an entrepreneurial environment that enables speed, collaboration, and global impact.
  • Grow in a People-Centered Culture. Thrive in a culture that values accountability, inclusion, and continuous development.
Job Scope

Supporting Instrument, Cassette and Reagent Manufacturing, in addition to, interfacing with Sourcing to develop and maintain the supplier quality improvement program.

Functioning as the Manufacturing interface with Engineering, Sourcing and Quality Assurance for supplier sourcing and supplier performance and participates or leads in Quality Control processes associated with setting appropriate raw material specification, test method development, product development, product sustaining engineering, automated inspection methods (CMM experience preferred), equipment and method validations, document development, and document and engineering change control. Participate in Material Review Board, Supplier Review Board and Supplier audits.

Frequent interaction with suppliers, intra-department interaction as well as, frequent inter-department interfaces with Purchasing, Quality Assurance, Instrument Manufacturing, Production Planning, Manufacturing Engineering, Research and Development (HW, SW, & Reagent), Cassette Manufacturing, Reagent Manufacturing, Reagent Quality Control and Document Control.

Duties and Responsibilities
  • Monitor and Measure supplier performance through measurement of production line statistics, Field data, company inspections, and audits.
  • Establish and report supplier quality metrics as required.
  • Utilize quality engineering principles and problem solving skills to develop and optimize supplier performance.
  • Assists in supplier selection & qualification process for new products and sourcing activities. Assess supplier production control and quality programs, identify shortfalls to expectation.
  • Participate in or lead the coordination of supplier conference meetings, site visits and audits.
  • Establish meetings with low scoring suppliers to communicate quality issues, discuss root cause and drive corrective actions.
  • Perform spec. reviews and correlate inspection methods between Luminex and its’ suppliers.
  • Act as the technical liaison between the suppliers and the manufacturing plants.
  • Work with critical suppliers to drive development and modification of purchased product’s test methods, test plans, and test fixtures.
  • Escalate Supplier problems and potential issues through management channels as necessary.
  • Drive continuous improvement projects with suppliers.
  • Assist with establishing annual CAPP objectives; fulfill individual CAPP objectives.
  • Participate in combined department operations as required.
  • Conduct or participate in applicable departmental and interdepartmental training.
  • Monitor procedural and engineering change releases; assess departmental impact.
  • Drive departmental document change control, manufacturer change control and engineering change control activities.
  • Lead or assist in specification development for raw materials, products, acceptance, etc.
  • Participate in product planning and product realization processes.
  • Participate…
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