Quality Technical Lead

As a Quality Technical Lead on our Fluke Health Solutions Quality Assurance team, you will be responsible for ensuring compliance with established ISO 17025 and other applicable regulatory standards and requirements. We are seeking a dedicated and detail‑oriented Quality Technical Lead to join our team. The Technical Lead will support the QC organization with any technical related issues, manage supplier quality, assist with problem‑solving using various tools, and ensure ISO 17025 compliance. Primary Contacts Internal: Quality Assurance and Regulatory Affairs team, Health Physics Team, Operations team, Engineering team, Business Units, and all other functional team members. External: Industry peers, Regulatory agencies, Customers, Notified Body, and Suppliers. Responsibilities Support QC team with any technical related concerns. Evaluate and monitor supplier performance and manage SCAR activities. Conduct supplier assessments aligned with ISO/IEC 17025 requirements and applicable regulatory expectations. Ensure compliance with ISO/IEC 17025 requirements, including calibration, traceability, and measurement practices. Support external audits and accreditation assessments (e.g., ISO/IEC 17025, NVLAP, regulatory audits) and serve as a key point of contact during audit activities. Conduct gap assessments and ensure readiness for external compliance evaluations. Apply strong problem‑solving skills, including root cause analysis (RCA), 5 Whys, and other quality tools to resolve nonconformances and drive corrective actions. Lead and execute independent QC‑related improvement projects, utilizing quality tools (Lean, Six Sigma, Kaizen) to enhance processes, reduce defects, and improve efficiency. Work in close collaboration with cross‑functional teams (Health Physics, Engineering, Operations, Regulatory, and Suppliers) to address quality issues and implement sustainable improvements. Support activities related to radiation measurement, dosimetry systems, and Health Physics practices, as applicable. Support NPI project on behalf of QC organization as needed. Qualifications BA/BS in Engineering, Physical Sciences, or Metrology Engineering background is preferred. 2-3 years of experience in a Quality or Health Physics role within manufacturing or laboratory environments. Strong knowledge of ISO/IEC 17025 requirements. Experience in calibration, testing laboratories, or measurement systems preferred. Health Physics experience or familiarity with radiation safety, dosimetry, or related regulatory frameworks is strongly preferred. Proven Experience Root cause analysis and structured problem‑solving methodologies. Leading independent improvement projects using quality tools. Cross‑functional collaboration to drive quality improvements. Strong communication, organization, and attention to detail. Benefits and Compensation Full‑time, onsite role based in Glenwood, IL. Competitive salary with a pay range of 70,600.00 - 117,900.00. Benefits include paid time off, paid holidays, and medical/dental/vision coverage starting on Day 1. Equal Opportunity Employer We Are an Equal Opportunity Employer. Fortive Corporation and all Fortive Companies are proud to be equal opportunity employers and are committed to providing reasonable accommodations for applicants with disabilities. #J-18808-Ljbffr Fortive Corporation