Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With rapid expansion across all our locations, we continue to push the boundaries of technology while fostering a dynamic, employee-centered culture. Our commitment to excellence and continuous improvement makes Resonetics an exciting place for professionals passionate about shaping the future of micro-manufacturing and being part of something bigger 

The principal responsibility of this position is to develop and maintain manufacturing processes to meet acceptable standards of manufacturability and compliance to the Resonetics Quality System. Manufacturing processes may include but are not limited to stamping, forming, shearing, machining (Wire EDM, Machining centers, etc.), laser welding, cleaning, automation and/or measurement. This position will work as part of a value stream team to concentrate on establishing and improving efficiencies in the manufacturing of medical devices. Additional areas of focus may include but are not limited to cost (scrap/labor/setup) reduction, statistical process control/variation reduction, work cell design/optimization, operator training/work instructions and tool/machine design selection or improvements.

Other responsibilities will include procedure generation, participation in production readiness/product validation activities for customers, developing and deploying continuous improvement plans for production products. An important aspect of this position is the hands-on nature of this role. As improvements are identified, it will very likely be the responsibility of this individual to implement and re-qualify changes.

Join Resonetics and be part of a team that’s redefining medical device manufacturing. If you’re passionate about innovation and thrive in a fast-paced environment, we’d love to hear from you. 

• Take ownership of specific manufacturing processes as they pass through the final stages of production readiness and process validation to ensure that quality awareness and product integrity are maintained.
• Lead or contribute to project teams responsible for implementing process improvements and new technologies.
• Determine job cost baselines and initiate cost reduction activities.
• Analyze and evaluate existing processes, manufacturing practices and systems to identify inefficiencies, bottlenecks, and areas for improvement.
• Develop or assist in design, costing, training for continuous improvement activities.
• Review existing process procedures for compliance to the designed process intent. Modify procedures as necessary and obtain approval from the originating process engineer.
• Set up and maintain Enterprise Resource Planning (ERP) for part numbers, including methods of manufacture, resource groups, part standards, etc.
• Provide technical support for process validation activities to ensure a smooth transition into the production environment.
• Perform Design of Experiments (DOE’s) where process optimization assessment is required.
• Develop process documentation and training where applicable (manufacturing process, tool/machine setup, preventive maintenance etc.).
• Periodic customer liaison for quality or continuation engineering related issues. May assume project manager role for specific customer applications.
• Daily/weekly/monthly of performance metrics.

• BS degree in engineering (mechanical, industrial or manufacturing disciplines) or 2-year technical degree with relevant manufacturing experience.
• Strong oral communication skills and demonstrated technical writing skills: able to perform data analysis, write detailed reports, comprehensive manufacturing procedures and assist Quality Engineering with validation protocols.
• Working knowledge of MS Office.

• Engineers with 2+ years’ experience or Technician with 4+ years’ experience in a manufacturing environment.
• New graduates with relevant intern/co-op work experience.
• Prior experience with any of the following manufacturing processes: stamping, forming, shearing, machining (Wire EDM, Machining centers, etc.), laser welding, cleaning, automation and/or measurement.
• Lean training, certification and experience.
• Working knowledge of statistical software and/or Minitab.
• Knowledge of SPC or other process capability analysis for determination of production readiness.
• Working knowledge of SolidWorks and/or AutoCAD.
• Working knowledge of Epicor/equivalent ERP
• Project management and leadership skills.
• Prior experience working in an engineering role within the medical device industry (ISO 13485) or other regulated industry.

• Ability to work in both an office and production/cleanroom environment.

The compensation for this role is competitive and will be based on experience and qualifications. The anticipated range is $60,000 -$91,000