Actalent
Quality Technician
Actalent - Providence, Rhode Island, United States, 02912
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Overview
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Overview
Quality Inspector
Perform dimensional and visual inspections on critical medical device components or assemblies using various measurement tools like calipers, micrometers, vision inspection equipment, gauges, etc. Conduct functional tests and verify conformance to detailed specifications and tolerances Interpret engineering drawings, specifications, and work instructions Record and maintain accurate inspection data, including lot history and traceability records Support lot release, material review, and root cause analysis for nonconforming parts Participate in audits and provide complete, well-organized inspection documentation Assist in implementing corrective actions and reinforcing compliance with ISO 13485 and FDA regulations Ensuring adherence to GDP (Good Documentation Practices) and GMP (Good Manufacturing Practices) requirements Nonconformance, CAPA, and Material Review Board Support Minimum 35 years of quality technical experience in the medical device industry required. Proven experience inspecting critical or high-precision components and/or devices. Familiarity with ISO 13485, and Good Documentation Practices (GDP). 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. 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) This is a fully onsite position in Providence,RI. This position is anticipated to close on Aug 11, 2025.
Perform dimensional and visual inspections on critical medical device components or assemblies using various measurement tools like calipers, micrometers, vision inspection equipment, gauges, etc. Conduct functional tests and verify conformance to detailed specifications and tolerances Interpret engineering drawings, specifications, and work instructions Record and maintain accurate inspection data, including lot history and traceability records Support lot release, material review, and root cause analysis for nonconforming parts Participate in audits and provide complete, well-organized inspection documentation Assist in implementing corrective actions and reinforcing compliance with ISO 13485 and FDA regulations Ensuring adherence to GDP (Good Documentation Practices) and GMP (Good Manufacturing Practices) requirements Nonconformance, CAPA, and Material Review Board Support Minimum 35 years of quality technical experience in the medical device industry required. Proven experience inspecting critical or high-precision components and/or devices. Familiarity with ISO 13485, and Good Documentation Practices (GDP). 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. 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) This is a fully onsite position in Providence,RI. This position is anticipated to close on Aug 11, 2025.