3 Days Left Manufacturing Engineer II
4 days ago
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
The Manufacturing Engineer 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 Engineer is expected to work cross functionally to reduce defects, scrap, cycle time, and increase yields.
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 Engineer 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 coordinates activities between all three departments, providing feedback to improve the product design and manufacturing processes to reduce quality defects and costs.
Responsibilities
1. Manage manufacturing processes and improvements in an Electro-Mechanical factory.
2. Work effectively with the production team, product development engineering team and quality team to provide support and resolve process and technical issues.
3. Create and execute verification and validation (IQ, OQ, PQ, FMEA), of product equipment, processes, and designs.
4. Review and update work instructions, ATP's, travelers and other internal documentation.
5. Analyze layout of equipment, workflow, assembly methods, and work force utilization to maximize efficiency.
6. Develop automated or semi-automated processes to improve efficiency and reliability.
7. Design, manufacture, and implement production tooling, jigs, dies and test equipment.
8. Review existing product designs and recommend changes to optimize product quality, minimize cost and ensure designs conform to production capabilities.
9. Coordinate production of prototypes, engineering builds, and process & product validations.
10. Track, document, investigate and analyze rejects and failures in production or customer returns and report design and process issues.
11. Participate in Failure Investigations and other CAPA related activities.
12. Perform tolerance analysis on mechanical and electrical assemblies.
13. Meet annual productivity improvement goals.
14. Ensure consistent professional communications with all VMCA team members.
15. Support VMCA's Quality Management System that establishes and maintains effective quality assurance processes and compliance to the International Standards: ISO13485, Canadian Medical Device Regulations (CMDR, SOR 98-292), FDA Quality System Regulations (QSR, 21 CFR Part 820) and the Medical Device Directive (MDD93/42/EEC).
Qualifications
1. Bachelor's Degree in Mechanical, Electrical, or Manufacturing Engineering.
2. P.Eng Eligible with EGBC.
3. 3+ years' experience.
4. Experience with medical device, aerospace and/or automotive design (or related field) in manufacturing environments.
5. Understanding of Lean and 6 Sigma Manufacturing principles.
6. Knowledge and understanding of manufacturing methods and processes.
7. Some experience with automation, robotics and PLC programming.
8. Understanding of electrical and mechanical design procedures and testing methodologies.
9. Analytical approach to problem solving.
10. Ability to find root cause and correct problems effectively.
11. Excellent analytical and judgment skills.
12. Hands-on laboratory or experimental experience.
13. The ability to read and interpret procedures and drawings.
14. Strong technical, analytical, interpersonal and organizational skills.
15. Ability to work well in cross-functional teams.
16. The ability to be dynamic and creative in identifying issues, their resolutions and in the execution of the resolutions.
17. The ability to remain open to new ideas and to maintain a positive attitude with a focus on quality.
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 - $66,509 - $88,230. (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.
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