R D Test Engineer - Medical Device #1379 Enhanced Compliance Inc. - 3.6 Waltham, MA Job Details 17 hours ago Qualifications Developing medical devices Laboratory safety GLP Content creation for technical audiences Defect resolution root cause analysis Quality control product testing Medical device testing Technical documentation 5 years Spreadsheets Defect analysis Regulatory compliance Equipment troubleshooting Mid-level Patient safety High school diploma or GED Collaboration with product development teams Analysis skills Laboratory reports Presentation skills Continuous improvement System validation Laboratory quality control Quality control problem-solving Engineering product development Technical troubleshooting support Data collection Root cause analysis Functional quality evaluation testing Technical writing experience within technology Full Job Description About ECI ECI's mission is to be the global leader of professional consulting services for the life sciences industry. Our clients lean on our diverse perspectives and decades of expertise to tackle their toughest challenges, and we take pride in providing them transformative solutions with distinctive, sustainable and long-term value. ECI boasts a proven track record of providing full product life cycle consulting on a variety of challenging and exciting projects. Our collaborative culture, welcoming team and flexible employment & benefit options allow us to maintain strong relationships with the most talented individuals in the life sciences industry. The R D Test Engineer supports the design and development of cutting-edge medical devices by collaborating closely with the Systems Engineering team. This role plays a key part in product testing, verification, and documentation, ensuring innovation aligns with design requirements. The ideal candidate is proactive, detail-oriented, and thrives in a collaborative R D environment focused on continuous improvement and technical excellence. What You'll Do Assist in the development, validation, and execution of test methods to support product and system verification activities. Perform product characterization and analysis on new and incoming products to ensure quality and functionality. Support troubleshooting of new products and processes related to design, materials, or manufacturing, identifying root causes and implementing lasting solutions. Maintain laboratory organization, equipment readiness, and compliance with safety and quality protocols. Prepare and maintain clear, detailed technical documentation and standardized reports to communicate results effectively within the technical and engineering teams. Demonstrate a strong commitment to patient safety and product quality by adhering to the company's Quality Policy, procedures, and regulatory requirements. What We Look For High School Diploma with 5+ years of experience in medical device development. Proven ability to work independently on complex technical tasks requiring critical thinking, problem-solving, and initiative. Skilled in identifying, defining, and resolving technical issues using a structured, analytical approach. Strong written and verbal communication skills for documenting and presenting technical data. Experience with laboratory testing, instrumentation, or product verification in a regulated industry (medical device experience preferred). Working knowledge of Good Laboratory Practices (GLP), validation protocols, and quality systems. Proficiency with data collection and analysis, including Microsoft Excel and similar programs ECI is an equal opportunity employer. All qualified applicants will receive consideration for employment at ECI without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law.