R&D Systems Technician

Job Description

Job Title: R&D Systems Engineering Technician

Duration: 6+ Months (Possible extension)

Location:
Waltham, MA 02452

Onsite Role

Responsibilities:

• Support the design, testing, and verification of innovative electrophysiology catheter systems.
• Will work closely with engineers to execute complex product testing, ensure robust documentation, and help bring cutting-edge technologies from concept to reality.
• Support the development, validation, and execution of test methods for product and system verification activities.
• Perform complex benchtop and system-level testing, including intricate physical setups involving catheter manipulation, fixture assembly, and precise alignment of electro-mechanical components.
• Operate computer-controlled test platforms, configure test parameters, execute semi-automated test sequences, and extract/analyze data using command-line scripts in Linux-based environments.
• Conduct product characterization and detailed analysis on new and incoming devices to verify quality, performance, and functionality.
• Maintain a well-organized laboratory environment, ensure equipment readiness, and strictly adhere to safety and quality protocols.
• Prepare clear, accurate, and detailed technical documentation and standardized test reports to effectively communicate results to engineering and cross-functional teams.
• Uphold the highest standards of patient safety and product quality by following the company’s Quality Policy, procedures, and all applicable regulatory requirements.

Education/Experience:

• High School Diploma (or equivalent) with 5+ years of relevant experience in medical device development or a highly regulated industry.
• Post-secondary education in a technical field (e.g., engineering technology, electronics, or mechatronics) is strongly preferred.
• Skilled at identifying, troubleshooting, and resolving technical issues using a structured and analytical approach.
• Ability to clearly document and present technical data.
• Hands-on experience with laboratory testing, instrumentation, and product verification in a regulated industry (medical device experience is highly preferred).
• Strong practical experience with electro-mechanical medical devices, including setup, operation, and troubleshooting of integrated hardware systems and precision assemblies.
• Experience interfacing with computer-based test systems and data acquisition tools, including Linux operating systems and command-line interfaces for data extraction and processing.
• Working knowledge of Good Laboratory Practices (GLP), validation protocols, and quality management systems.