Manufacturing Technologist

Verathon is a global medical device company committed to being a trusted partner to our customers and advancing patient care through innovative Airway Management and Urology solutions. For more than 40 years, we have worked alongside healthcare professionals to understand their needs and deliver high-quality technologies that provide lasting clinical and economic value.

Our portfolio includes leading Glide Scope®video laryngoscopy and BFlex™ bronchoscopy solutions, Bladder Scan®bladder volume measurement, and a growing range of single-use Urology solutions. Behind our innovations is a diverse, global team united by a commitment to our customers, collaboration, and improving patient care.

Verathon, a business unit of Roper Technologies, is headquartered in Bothell, Washington, with international subsidiaries in Canada, Europe, and Asia Pacific.

The swing shift Manufacturing Technologist is responsible for troubleshooting hardware & system issues in support of our sustaining medical devices and products as well as supporting new product introduction. The Manufacturing Technologist is expected to work cross functionally to reduce defects, scrap, cycle time, and increase yields. This position is on the swing shift Monday through Friday 3:30pm to 12:00am.

Verathon believes that People are the Source of our Strength! Employees that consistently demonstrate skill, loyalty, initiative, innovation, enthusiasm and team spirit are what make the VMCA team the best in the industry! The Manufacturing Technologist works closely with the Manufacturing Engineering Team and is responsible for providing technical support to the Production, Quality Assurance and Product Development Engineering teams. This position requires close communication and coordinated activities between all three departments, providing feedback to improve the product design and manufacturing processes to reduce quality defects and costs.

• Working hours are swing shift Monday through Friday 3:30pm to 12:00am
• Manage manufacturing processes and improvements in an Electro-Mechanical factory
• Work effectively with production team, product development engineering team and quality team to provide support and resolve process and technical issues
• Execute verification and validation (IQ, OQ, PQ, FMEA), of product equipment, processes, designs review and update work instructions, ATP's, travelers and other internal documentation
• Maintain automated or semi-automated processes
• Maintain production tooling, jigs, dies and test equipment
• Track, document, investigate and analyze rejects and failures in production or customer returns and report design and process issues
• Participate in product Failure Investigations and other CAPA related activities
• Preventative Maintenance of production equipment
• Ensure consistent professional communications with all VMCA team members
• Support VMCA's Quality Management System that establishes and maintains effective quality assurance processes and compliance to the International Standards: ISO
  13485, Canadian Medical Device Regulations (CMDR, SOR 98-292), FDA Quality System Regulations (QSR, 21 CFR Part 820) and the Medical Device Directive (MDD
  93/42/EEC).

• Understanding of electrical and mechanical design procedures and testing methodologies
• Analytical approach to problem solving
• Experience and aptitude in Design of Experiments, ability to find root cause and correct problems effectively
• The ability to read and interpret procedures and drawings
• Strong technical, analytical, interpersonal and organizational skills
• Ability to work well in cross-functional teams
• The ability to be dynamic and creative in identifying issues, their resolutions and implementing resolutions
• The ability to…