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Job Requirements of R&D Systems Engineering Technician:
-
Employment Type:
Contractor
-
Location:
Waltham, MA (Onsite)
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R&D Systems Engineering Technician
Careers Integrated Resources Inc
Waltham, MA (Onsite)
Contractor
Job Title: R&D Systems Engineering Technician
Location: Waltham, MA, 02452
Duration: 6 Months+ (Possible Extension)
Pay Range: $35 to $44.00/hr. on W2
Shift Time: 08:00 AM - 04:30 PM
Job Overview
- We are seeking a talented, hands-on R&D Systems Engineering Technician to join the Systems Engineering team in the development of nextgeneration 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 cuttingedge technologies from concept to reality.
- The ideal candidate is proactive, detailoriented, technically strong, and thrives in a fastpaced, 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 systemlevel testing, including intricate physical setups involving catheter manipulation, fixture assembly, and precise electromechanical alignment.
- Operate computercontrolled test platforms by configuring test parameters, executing semiautomated test sequences, and extracting/analyzing data using commandline scripts in Linuxbased 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 crossfunctional 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, problemsolving 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.
- Handson experience with laboratory testing, instrumentation, and product verification in regulated environments.
- Strong practical experience with electromechanical medical devices, including setup, operation, and troubleshooting of integrated hardware systems and precision assemblies.
- Experience working with computerbased test systems and data acquisition tools, including Linux operating systems and commandline interfaces.
- Working knowledge of Good Laboratory Practices (GLP), validation protocols, and quality management systems.
- Postsecondary education in a technical field such as Engineering Technology, Electronics, or Mechatronics.
- Prior medical device industry experience.
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