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Manager, Supplier Quality Engineering

Verathon Inc.
life insurance, paid time off, paid holidays, 401(k)
United States, Washington, Bothell
20001 North Creek Parkway (Show on map)
Jan 09, 2026

Manager, Supplier Quality Engineering
Location

US-WA-Bothell
ID

2025-1671



Category
Quality Assurance/Regulatory Affairs

Position Type
Full Time

Work Model
Onsite



Company Overview

Verathon is a global medical device company focused on supporting customers by being their trusted partner, delivering high-quality products that endure over time and ensure clinical and economic utility. Two areas where Verathon has significantly impacted patient care, and become the market leader in each, are bladder volume measurement and airway management. The company's BladderScan portable ultrasound and GlideScope video laryngoscopy & bronchoscopy systems effectively address unmet needs for healthcare providers and meaningfully raise the standard of care for patients. Verathon, a subsidiary of Roper Technologies, is headquartered in Bothell, Washington, USA and has international subsidiaries in Canada, Europe and Asia Pacific. For more information, please visit www.verathon.com.



Overview

Verathon is looking for a Manager, Supplier Quality Engineering to become the newest member of our Quality Assurance Team located in Bothell, WA.
The Manager of Supplier Quality Engineering is responsible for managing, improving, and maintaining the Verathon Global Supplier Quality Program.



Responsibilities

* Set strategy for global Supplier Quality organization
* Provide leadership to Supplier Quality Engineers; manage performance through clear goal and expectation setting, accountability, and feedback; maximize the contributions of team members by proactively developing talent
* Manage team performance through KPIs/metrics that track team activities and deliverables
* Represent Verathon as the primary liaison with contract manufacturers and suppliers for all quality and compliance activities
* Develop and implement effective Quality Management System (QMS) processes in compliance with governing regulations and international standards: FDA Quality System Regulations (QSR, 21 CFR Part 820), Canadian Medical Device Regulations (CMDR, SOR 98-292), EU Medical Device Regulation (2017/745), ISO13485, and ISO14971
* Mitigate risks that may affect product quality or regulatory compliance
* In partnership with Supply Chain Management, improve and manage processes to select new suppliers
* Manage component qualification /Production Part Approval Process (PPAP) in alignment with New Product Development and Sustaining Engineering timelines; Ensure adequate process development and validation (IQ/OQ/PQ) occurs for suppliers' manufacturing processes
* Define and execute a risk-based Supplier Quality Audit program; Conduct audits of suppliers to assess the robustness of their Quality Systems, controls, and ability to deliver quality parts
* Manage supplier-caused non-conforming material (NCM) through Return to Vendor (RTV) and the Supplier Corrective Action Request (SCAR) processes
* Lead investigation and correction of product quality issues
* Ensure suppliers properly execute responsibilities under the Supplier Change Notification (SCN) process
* Manage tools and mechanisms for ensuring supplier performance (Supplier Quality Agreements and Supplier Scorecards)
* Lead continuous improvement in QMS and suppliers' manufacturing processes
* Leverage lean and six sigma methodologies.



Qualifications

* Bachelor's degree and 8+ years of Quality experience (including 4 years' experience in supplier quality roles) or master's degree and 6+ years of Quality experience
* 3+ years prior experience as a people leader
* Bachelor's degree required
* Mechanical, Electrical, or Biomedical Engineering or Business Management (Supply Chain) Degree is preferred
* Experience in Aerospace (AS9145 APQP/PPAP) or medical device (ISO 13485) industries is preferred
* Skill in analytical problem solving, root cause analysis, and driving corrective actions required
* Professional interpersonal and communication skills
* Ability to build relationships with key personnel in supplier organizations
* Ability to ask the hard questions while still maintaining collaborative relationships, particularly in the investigation and resolution of product quality issues
* Experience and aptitude as a Quality Management System Lead Auditor required
* ASQ Certification, such as Certified Manager of Quality/Organizational Excellence (CMQ/OE), Certified Quality Engineer (CQE), Certified Reliability Engineer (CRE), Certified Quality Auditor (CQA) is preferred
* Experience in product safety (IEC 60601 Standards) is preferred
* Experience in Lean Six Sigma is preferred
* Ability to work under time constraints to meet strategic objectives
* Ability to prioritize effectively and deliver results
* Ability to travel up to 25% with international travel required

Salary range - $116,508.00 - $158,899.00 (Compensation will vary based on skills, experience and location; it is not typical to be hired at or above the top of the salary range).

Full-time employees who are not on a commission plan are eligible for Verathon's annual bonus plan based on company and individual performance.

Verathon provides a competitive benefits package including medical, dental, vision, basic life insurance, paid holidays, paid time off and a 401(k) matching plan. For more information, please visit our complete Benefits Summary at https://www.verathon.com/US-HQ-Employee-Benefits-Summary.



EEO

Research shows that women and underrepresented groups tend to apply to jobs only when they check every box on a job posting. If you're currently reading this and hesitating to click "Apply" for that reason, we encourage you to go for it! Even if you are not a match for this role, we may have another opportunity that may be a great fit.

Verathon is an equal opportunity employer and strongly supports diversity in the workplace. We believe that diverse ideas, opinions and perspectives will build a strong foundation for success. In order to provide equal employment and advancement opportunities to all individuals, employment decisions at Verathon will be based on merit, qualifications, and abilities. Verathon does not discriminate in employment opportunities or practices on the basis of race, color, religion, sexual orientation, gender identity, national origin, age, disability, or any other characteristic protected by law.
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