- Location
- Nashua, NH, US
- Type
- Full-time
- Department
- Engineering
- Education
- High School
- Visa
- Not sponsored
- Closing date
- Today
- Source
- iCIMS
Description
Overview
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.
Primarily responsible for assembling complex medical devices for projects in Phase 3 (Design Verification). Assist Design and Development Engineers and Technicians in meeting quality specifications on Design and Development projects. Assist in transitioning Design and Development projects to production in a small team and collaborative environment.
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.
Responsibilities
- Efficiently, effectively, and consistently assemble and package complex medical devices
- Accurately and promptly fill out quality assurance records
- Conduct incoming, in process and final inspection of components, assemblies and finished goods
- Assist in inventory management
- Other duties as assigned
Required Qualifications
- High School diploma or Equivalent
- Ability to adapt quickly and positively to changing priorities and processes
- Ability to work under minimal supervision
- Ability to effectively use basic measurement tools including but not limited to rulers, calipers, micrometers, and pin gauges
Preferred Qualifications
- Experience with laser welding processes and techniques
- Experience with catheter processing equipment including hot boxes, laminators, split die bonders and tipping machines
- Experience working in a Controlled Environment Room (CER)
- Familiarity with ISO Quality Systems particularly in medical device development and manufacturing
- Ability to read, comprehend and perform processes documented in MPIs
- Ability to read and understand engineering drawings
- Ability to create job related records for quality purposes
Physical Demands
- Standing and walking for short periods of time.
- Ability to use a microscope, including manipulating small object under a microscope for long periods of time.
Compensation
- The compensation for this role is competitive and will be based on experience and qualifications. The anticipated range is $44.8K-$58K
- Our company policy is that we are unable to provide visa sponsorship. Candidates must already be legally authorized to work in the United States without the need for sponsorship now or in the future.