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.

The Quality Technician III is responsible for supporting the Quality activities within the Operations area. Primary responsibilities include application of Quality tools in investigating issues and compiles corresponding reports. Collaborates with functional teams (Manufacturing Engineering, R&D) and supports daily operation's needs. Proficient in use of databases, manufacturing processes, operation processes. Supports quality with process data, support of non-conforming product processes, and investigations into production related quality issues.

• Support Verathon’s Global Quality Management System.
• Support with part/product failure investigations, root cause and other CAPA related activities, with hands-on operational support, including the design and use of jigs and fixtures to optimize new equipment functionality.
• Review statistical rationale to analyze, and interpret daily operations defect data, to seek out opportunities for improvement.  
• Control non-conforming parts and products to prevent unintended use, including maintenance of records, disposition, and verification.
• Identify, control, and document potential product, process, and/or quality system nonconformances, and escalate issues as needed to ensure resolution.
• Collaborate with Manufacturing Engineering in managing and processing non-conforming materials.
• Write, update, collaborate with other functional teams, launch quality documentation in accordance with Verathon’s Change Control process.
• Maintain accurate and organized quality records in alignment with established procedures and regulatory requirements.
• Assist in the planning and execution of quality audits to ensure compliance with internal and external standards.
• Support the resolution of internal audit findings by assisting in investigations, collaborating with cross-functional teams to gather necessary information, helping identify root causes, and ensuring findings are documented and addressed within set deadlines.
• Provide support for Inspections and engineering changes as required.
• Analyze quality data to identify trends, troubleshooting issues, and recommend improvements to enhance product quality.
• Assist QA/Manufacturing Engineering team in writing and executing process validation protocols, support manufacturing for pFMEA, validation activities, including upkeep of MVP (Master Validation Plan).
• Provide ongoing Quality Assurance support to production lines, the service department, and subsidiaries to ensure quality standards are maintained.
• Support the Ship Holds process to ensure timely and accurate resolution of any quality-related shipping issues. 
• Provide back up on other QA functions as required.
• Follow all company policy and procedures.
• Other duties as assigned by supervisor or manager.

• 2-3 years of experience in a quality function is required; Within the medical device, pharmaceutical, or aerospace industry preferred.
• A diploma in Engineering Technology (Electrical, Mechanical, Biomedical) or a Bachelor of Science degree, with preference given to candidates holding a degree.
• Preferred eligibility for EIT (Engineer In Training) registration with EGBC. 
• Detail-oriented individual capable of performing daily tasks with limited supervision.
• Ability to read and interpret procedures and basic technical drawings.
• Ability to accurately use basic measuring devices, including experience with Optical Measuring Machine (OMM).  
• Familiarity with ISO 13485 and FDA cGMP regulations desirable
• Proficient with MS Office Software
• Experience with an ERP system
• Ability to follow strict safety requirements
• Self-starter who demonstrates an aptitude for organization
• Ability to handle multiple projects and meet strict deadlines
• Ability to lift-up to 40 lbs

Why Join Us?

• Be part of an innovative team that is dedicated to improving patient outcomes.
• Engage in meaningful work that makes a difference in the healthcare industry.
• Competitive salary and comprehensive benefits package.
  • Salary range - $55,005 – $75,450 (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 a generous HCSA, paid holidays, paid time off and a retirement matching plan.