Job Title: Quality TechnicianJob Description We are seeking a dedicated Quality Technician to perform dimensional and visual inspections on critical medical device components or assemblies. This role involves using various measurement tools like calipers, micrometers, vision inspection equipment, and gauges to ensure components meet detailed specifications and tolerances. You will interpret engineering drawings, specifications, and work instructions, recording and maintaining accurate inspection data, including lot history and traceability records. Additionally, you will support lot release, material review, and root cause analysis for nonconforming parts, participate in audits, and provide complete, well-organized inspection documentation. You will assist in implementing corrective actions and reinforcing compliance with industry and FDA regulations, ensuring adherence to Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) requirements. Responsibilities + Perform dimensional and visual inspections on medical device components using measurement tools. + Conduct functional tests and verify conformance to specifications and tolerances. + Interpret engineering drawings, specifications, and work instructions. + Record and maintain accurate inspection data and traceability records. + Support lot release, material review, and root cause analysis for nonconforming parts. + Participate in audits and provide organized inspection documentation. + Assist in implementing corrective actions and reinforcing compliance with regulations. + Ensure adherence to GDP and GMP requirements. + Support nonconformance, CAPA, and Material Review Board activities. Essential Skills + Minimum 3–5 years of quality technical experience in the medical device industry. + Proven experience inspecting critical or high-precision components and devices. + Familiarity with Good Documentation Practices (GDP) and GMP. + Proficiency with inspection equipment and interpreting engineering drawings and GD&T. + Experience using Excel, electronic QMS platforms (e.g., Minitab, ETQ, Master Control), and document control systems. + Excellent attention to detail, organization, and communication skills. Additional Skills & Qualifications + CQI or CQT certification. + Experience with cleanroom manufacturing in a medical device setting. + Working knowledge of SPC and data analysis tools such as Minitab. + Familiarity with Failure Investigation techniques. Work Environment This position is based in a manufacturing environment within a very clean, modern facility. Pay and Benefits The pay range for this position is $52000.00 - $70000.00/yr. Health InsuranceDental InsuranceVision InsuranceDisability Insurance (likely includes both short- and long-term)401(k) Retirement PlanVariable Compensation Plan (performance-based bonuses or incentives) Workplace Type This is a fully onsite position in Cranston,RI. Application Deadline This position is anticipated to close on Aug 15, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.