Operator IVResonetics 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 Operator IV role will be responsible for conducting complex NPI build/assembly operations, technical support for R&D programs, testing of product, and product development activities. 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:- Work with project team, Line Lead, or Supervisor to ensure customer demand and the production schedules are met
- Read work orders, follow production drawings and sample assemblies, receive verbal instructions regarding duties to be performed, and complete necessary SWO's or work orders as required
- Report problems or concerns with quality, processes, engineering, equipment, materials, or labor the supporting engineer, project team, lead, or supervisor
- Accurately complete all essential documents (i.e., Lab Notebooks, Device Master Records (DMR's), Lot History Records (LHR's), Inspection Records and Validation DocumentationProvide training to new team members and provide cross-training for current team members
- Record observations of both assembly processes and assembly (or component) performance
- Identify opportunities for productivity and quality improvements
- Ensure equipment is maintained and calibrated within defined timelines, when possible, in order to minimize interruption to production lines
- Adjusts and trims materials from components to achieve specified medical or dimensional characteristics
- Maintain a clean, safe, and organized work environment
Support company finance, accounting, human resources, quality, regulatory, and clinical departments as necessary to ensure compliance with requirements.
Required Qualifications:- High school graduate or GED equivalent 10+ years of assembly and/or manufacturing experience with increasing complexity
- Demonstrated ability to read and understand measurement equipment (e.g., caliper, ruler, micrometer, microscope)
- Working knowledge of Good Manufacturing Practices (GMP)
- Ability to work independently with little oversight and apply critical reasoning skills
- Accurately read work orders, following production drawings, and receive instruction
- Accurately complete all essential documents (Lab Notebooks, Device Master Records, Lot History Records, Inspection Records, and Validation Documentation)
- Experience ausing a microscope in assembly, working with different types of catheter materials, or other similar medical devices with small parts
- Ability to handle and be trusted with confidential and/or sensitive
to work in a fast-paced, constantly changing environment.
Ability to be flexible and to handle multiple projects in an organized, timely manner.
Able to problem-solve, work under pressure, and to effectively manage stress.
Ability to work overtime as needed
Physical Demands
Prolonged periods of sitting at a desk and working on a computer and/or microscope
Prolonged periods of standing and/or walking
Must be able to lift up to 25 pounds at times
Manual dexterity in order to assemble products or machines as directed
Excellent hand-eye coordination
Ability to differentiate between colored wires, tabs, and electronic components
Must wear gown, gloves, and ear protection when applicable
Must be willing to work in lab and clean room environments to support project work
CompensationThe compensation for this role is competitive and will be based on experience and qualifications. The anticipated range is $24.00–$31.00/hr.
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.
