Job ID: JOB_ID_1193
Role Overview: R&D Test Engineer (Medical Device)
We are seeking a highly skilled and detail-oriented R&D Test Engineer to join our innovative team in Irvine, CA. This is a long-term contract position focused on the development and optimization of testing methodologies for cutting-edge medical devices. The successful candidate will play a critical role in ensuring the safety, reliability, and performance of high-density multi-electrode components and other advanced medical technologies. This role requires a deep understanding of the medical device domain, specifically adhering to the rigorous standards set by federal, state, and corporate guidelines, including those of Johnson & Johnson.
Key Responsibilities and Duties
- Test Method Development & Automation: You will be responsible for developing and optimizing sophisticated test methods to support the characterization and verification of medical device components. A primary focus will be on automating simulated use test setups to reduce manual intervention, increase throughput, and enable extended continuous testing cycles.
- Scripting and Hardware Integration: Build robust test scripts, instrument control logic, and hardware automation solutions to streamline complex testing workflows.
- Prototyping & Fixture Design: Design, prototype, and refine 3D-printed test fixtures. These fixtures are essential for evaluating early-stage prototypes and meeting pre-clinical testing requirements.
- Component Assembly: Construct and assemble sample components to support device performance testing, characterization, and feasibility studies.
- Process & Equipment Evaluation: Evaluate and optimize settings on new manufacturing printers, including high-precision additive manufacturing systems, to determine suitable parameters for producing high-density components.
- Experimental Documentation: Conduct experiments and document configurations that improve electrode impedance and signal-to-noise ratio (SNR).
- Cross-Functional Collaboration: Collaborate closely with manufacturing engineers to ensure that test findings translate effectively into scalable production processes.
- Data Analysis & Reporting: Analyze complex test data, summarize findings, and communicate insights to cross-functional R&D, quality, and manufacturing teams. Maintain clear, accurate engineering documentation, test protocols, and technical reports.
Required Qualifications and Skills
- Experience: Minimum of 5 years of professional experience specifically within the Medical Device Domain.
- Technical Proficiency: Proven ability to develop and optimize testing, automate test setups, and build test scripts.
- 3D Printing: Hands-on experience in designing and refining 3D-printed fixtures for engineering applications.
- Communication: Exceptional oral and written communication skills in English are mandatory.
- Soft Skills: Ability to multitask, prioritize responsibilities, and provide immediate responses in a fast-paced environment. Must be able to follow complex written procedures and function effectively within a team-oriented environment.
Work Environment and Compliance
This position operates under limited supervision and requires strict adherence to all applicable federal, state, and local laws and regulations. Candidates must be prepared to work onsite in Irvine, CA, and contribute to a culture of excellence and safety. The role involves significant interaction with R&D and Quality departments to ensure all device performance testing meets the highest industry standards.
Special Requirements
Minimum 5 years experience in Medical Device Domain. Long-term contract. Onsite requirement in Irvine, CA.
Compensation & Location
Salary: $115,000 – $165,000 per year (Estimated)
Location: Irvine, CA
Recruiter / Company – Contact Information
Recruiter / Employer: Valzo Soft Solutions
Email: prince@valzosoft.com
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