The Leader in Advanced Engineering, Prototyping, Automation, and Micro Manufacturing for MedTech Markets Globally
Nashua, New Hampshire
Resonetics is a pioneer in advanced engineering and manufacturing solutions for the life sciences industry. Core capabilities include laser ablating, cutting, drilling and welding; nitinol shape setting and electropolishing, centerless grinding and photochemical machining, fiber optic sensing and thin wall tube fabrication. With Lightspeed Application Development Labs located strategically to serve MedTech companies around the world, Resonetics is built on a foundation of quality, speed and innovation to deliver best-in-class value with a customer centric approach. For over 30 years, Resonetics has been a pioneer in micro manufacturing. Founded in 1987, Resonetics has continuously invested in leading edge technology to solve medical device manufacturing challenges and developing experts who innovate tomorrow’s medical devices. We have deployed over 500 laser workstations that cover a wide spectrum of laser types and wavelengths – femtosecond, picosecond, excimer, DPSS, and CO2. Combining state-of-the-art laser systems with a top technical team allows Resonetics to partner with customers and provide winning solutions that meet technical as well as economic requirements. Resonetics has 14 manufacturing facilities located in the United States, Canada, Costa Rica, Israel and Switzerland with ISO-13485:2003 certified quality system and lean six-sigma practices.
On-site · Montréal
The QA Inspector is responsible for inspecting incoming materials and performing final testing on medical devices in a cleanroom environment. They ensure all operations comply with ISO 13485, FDA, and GMP standards while documenting results and managing nonconformities.
On-site
Overview Reporting to the Senior Manager, Production, this member of the Production team is responsible for assembling medical devices components for Agile MV Technologies Inc (A Resonetics Company) products. Ensuring the smooth running of all operations activities in line with ISO 13485, FDA, GMPs, CE mark such as the following tasks. Responsibilities Assemble small components with a microscope, equipment, and tools. Ability to follow the work instruction and execute them effectively. Follow procedures according to the ISO 13485 Quality Management System. Maintain a clean and orderly worksta…
On-site · Montréal
Assist in the product development process from concept to final design review for mechanical components of medical devices. Ensure all operations comply with ISO 13485, FDA, and GMP standards while refining manufacturing processes.
