Medical Device R&D Technicians
Pay $35.00 - $40.00
6 month+ assignment
Onsite in Campbell, CA
participate in developing surgical hardware that will utilize your skills in mechanical assembly, electrical cable routing, soldering mounting of circuit boards, and debugging. Your work will directly contribute to improving access to care that gives stroke patients a better chance to survive and thrive.
Demonstrated history of working on complex mechanical and electrical systems.
• HS diploma and a minimum of 8 years related experience; AA degree and a minimum of 5 years experience preferred.
• Strong understanding of assembly and calibration methods.
• A proven ability to work well in a team environment
• Must be capable of working independently and in a team while being flexible and self-motivated.
• Previous experience assembling Medical Devices in an FDA-regulated environment is preferred.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Assemble complex mechanical systems that encompass hundreds of unique parts. Your expertise with precision tools will ensure the accurate placement of linear guides, rotary bearings, actuators, motors, and drive systems.
• Construct electrical cables to power drive systems and sensor architecture. This involves creating cable assembly prints, attaching electrical connectors, and troubleshooting using voltmeters and oscilloscopes. You will take a leadership role in developing optimal cable routing, documenting it through technical drawings and pictures.
• Perform electrical board bring-up, soldering of simple components or circuits, and characterization testing of electrical subsystems. Thoroughly document test results.
• Collaborate closely with engineers to develop work instructions, maintain inventory for development builds, and ensure a clean and organized build environment.
• Maintain and calibrate tools, replenish stock fasteners, and ensure organization in the development and build areas.
• Conduct long-term verification tests like mechanical life test or thermal cycling.
• Actively promote and support the Quality Management System, Quality Objectives, and Quality Policy.
• Assure that you and functional subordinates (if applicable) are trained on all applicable procedures and processes according to Good Manufacturing Practices, and applicable FDA and Regulatory requirements.
• Actively promote and support the company’s Management Review process.
• Inform responsible personnel of concerns involving product quality.
Benefits (employee contribution):
All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act
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