Quality Technical Lead

Description

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. The incumbent will support the QC organization with technical issues, manage supplier quality, assist problem-solving with various tools, and uphold ISO 17025 compliance. This full‑time, on‑site role based in Glenwood, IL includes competitive salary, paid holidays, PTO, and medical/dental/vision coverage starting Day 1;

we value your whole self at FHS.

Internal:
Quality Assurance and Regulatory Affairs team, Health Physics Team, Operations team, Engineering team, Business Units, and other functional team members. External:
Industry peers, Regulatory agencies, Customers, Notified Body, Suppliers.

• Support QC team with technical concerns.
• Evaluate and monitor supplier performance and manage SCAR activities.
• Conduct supplier assessments aligned with ISO/IEC 17025 requirements and 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 key point of contact during audit activities.
• Conduct gap assessments and ensure readiness for external compliance evaluations.
• Apply strong problem‑solving skills (root cause analysis, 5 Whys, 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.
• Collaborate 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 projects on behalf of the QC organization as needed.

• BA/BS in Engineering, Physical Sciences, or Metrology Engineering background (preferred).
• 2–3 years of experience in a Quality/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 (strongly preferred).

• 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.

The salary range for this position (in local currency) is 70,600..

We Are an Equal Opportunity Employer. Fortive Corporation and all Fortive Companies are proud to be equal opportunity employers. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity or expression, or other characteristics protected by law. Fortive and all Fortive Companies are also committed to providing reasonable accommodations for applicants with disabilities.

Individuals who need a reasonable accommodation because of a disability for any part of the employment application process, please contact us at