What are the responsibilities and job description for the Research And Development Technician position at Integrated Resources, Inc ( IRI )?
Job Title: R&D Systems Engineering Technician
Location: Onsite, Waltham, MA 02452
Duration: 6-month W2 contract with high possibility of extension based on performacne and business needs
Job Overview
We are seeking a talented, hands-on R&D Systems Engineering Technician to join the 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 collaborate closely with engineers to execute complex product testing, maintain robust documentation, and help transition cutting‐edge technologies from concept to reality. The ideal candidate is proactive, detail‐oriented, technically strong, and thrives in a fast‐paced, collaborative R&D environment focused on continuous improvement and technical excellence.
Key Responsibilities:
- 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 electro‐mechanical alignment.
- Operate computer‐controlled test platforms by configuring test parameters, executing semi‐automated test sequences, and extracting/analyzing 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 clean, 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 communicate results to engineering and cross‐functional teams.
- Uphold the highest standards of patient safety and product quality by complying with the company Quality Policy, procedures, and applicable regulatory requirements.
Qualifications & Skills
Required
- High School Diploma (or equivalent) with 5 years of relevant experience in medical device development or another highly regulated industry.
- Ability to work independently on complex technical tasks with strong critical thinking, problem‐solving skills, and initiative.
- Demonstrated experience identifying, troubleshooting, and resolving technical issues using structured and analytical approaches.
- 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 regulated environments.
- Strong practical experience with electro‐mechanical medical devices, including setup, operation, and troubleshooting of integrated hardware systems and precision assemblies.
- Experience working with computer‐based test systems and data acquisition tools, including Linux operating systems and command‐line interfaces.
- Working knowledge of Good Laboratory Practices (GLP), validation protocols, and quality management systems.
Preferred
- Post‐secondary education in a technical field such as Engineering Technology, Electronics, or Mechatronics.
- Prior medical device industry experience.