R&D Systems Engineering Technician

R&D Systems Engineering Technician

Job Summary:

Talent Software Services is searching for an R&D Systems Engineering Technician for a contract position in Waltham, MA. The opportunity is for six months with a strong chance for a long‑term extension.

Position Summary:

We are seeking a talented and hands‑on R&D Systems Engineering Technician to join our Systems Engineering team in the development of next‑generation medical devices. In this critical role, you will support the design, testing, and verification of innovative electrophysiology catheter systems. You will work closely with engineers to execute complex product testing, ensure robust documentation, and help bring cutting‑edge technologies from concept to reality.

The ideal candidate is proactive, technically skilled, detail‑oriented, and thrives in a fast‑paced, collaborative R&D environment where continuous improvement and technical excellence are valued.

• 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.

• 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.
• Proven ability to work independently on complex technical tasks, demonstrating strong critical thinking, problem‑solving skills, and initiative.
• Skilled at identifying, troubleshooting, and resolving technical issues using a structured and analytical approach.
• Excellent written and verbal communication skills, with the 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.