Medical Device QA
731 open positions
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Compliance and Quality Specialist (CAPA) PhilipsTaguig, PH 10d Lead analysis of defects and non-conformances, manage dispositions, and facilitate Corrective and Preventive Actions (CAPA) to ensure regulatory compliance and patient safety.
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Quality Engineer II FreseniusmedicalcareReynosa, TAMPS, MEX 10d Ensuring product quality, regulatory compliance, and continuous improvement in a regulated medical device manufacturing environment.
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Quality Assurance Specialist TempusChicago $55k–$55k10d Ensuring compliance with FDA QSR, ISO 13485, and CLIA/CAP regulations by managing incidents, deviations, nonconformances, and corrective/preventive actions (CAPA) in clinical molecular testing laboratories.
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Compliance Manager (all genders) Avelios-MedicalMunich 10d Manage compliance activities, risk, and quality management to ensure regulatory adherence and patient safety in a healthcare software platform.
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Senior Manager QA (Medtech) DanaherBangalore, Karnataka, India 10d Lead QA Design Control and Supplier Quality initiatives to ensure safe, compliant, and innovative medical devices during new product development and maintenance.
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Quality Engineer II↗ Bd SingaporeTuas, S00, SG 10d Ensure compliance with ISO 13485, FDA 21 CFR Part 820, and international regulatory requirements while supporting design control, risk management, and continuous quality improvement in a regulated medical device environment.
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Customer Experience Engineer AbbottUnited States - Minnesota - Plymouth 10d Critical link between customers, clinicians, and internal product teams to ensure medical device quality, safety, and performance through complaint investigations and root cause analysis.
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Sr. Clinical Quality Manager MedtronicLafayette, Colorado, United States of America $162k–$162k10d Provide strategic leadership for clinical quality systems, compliance, and operational excellence across the Surgical CMAH organization to protect patients and ensure regulatory integrity.
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Quality System Manager (Temporary contract)↗ EcolabBarcelona, CT, ES 10d Manage Quality Management Systems compliance for Ecolab's Healthcare Europe operations, ensuring adherence to MDR and ISO 13485 standards while driving continuous improvement.
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Engineer II, NPD- Quality EdwardsUSA - California – Irvine $87k–$123k10d Develop experiments and tests to validate and improve medical device manufacturing processes and products, ensuring compliance with regulatory requirements and quality systems.
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Quality Assurance Technician II (Fixed-Term) MeritSouth Jordan, UT 10d Support Post Market Surveillance and Recall/Field Action personnel with quality system documentation, product tracking, inspection support, and administrative execution of quality activities in a regulated medical device environment.
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Senior Quality Engineer↗ StrykerKalamazoo, MI, US $78k–$78k10d Develop and implement quality methods, process control, inspection, and testing to ensure medical device products meet regulatory and design standards.
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Quality Engineer II↗ Zimmer BiometBogotá, CUN, CO 10d Formulates procedures, specifications, and standards for Zimmer products and processes; develops corrective/preventative action plans; collects and analyzes data for gauge and product evaluation.
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INGENYX - Quality Engineer 3↗ TeleflexTrenton, GA, US 10d Lead Quality Engineering activities for manufacturing operations, focusing on nonconformance resolution, customer complaint investigations, and process validations.
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Quality Engineer - Multiport Da Vinci IntuitiveSunnyvale, CA, us 11d Owns product, process, and complaint investigations for the Endoluminal product family; serves as escalation owner for quality risks; leads risk assessments and continuous improvement projects.
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Senior Quality Assurance Engineer EnvistaSWE - Karlskoga - Nobel Biocare AB 11d Ensuring quality management and assurance processes for medical device manufacturing at a production site, supporting compliance with ISO13485 and FDA QMSR regulations.
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Manager, Quality, PPC - Surgery GehcSalt Lake City, US 11d Ensures quality and regulatory compliance for a large medical device facility while driving process efficiency and leading supply chain quality activities.
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Quality Assurance Manager, Medical Device & Combination Products↗ PfizerKalamazoo, MI, US $89k–$89k11d Ensure medical devices and combination products are developed and maintained in compliance with design control requirements and regulatory standards (21 CFR 820, ISO 13485, ISO 14971) across the product lifecycle.
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QE Complaints BdxUSA NE - Columbus (West) 12d Lead quality engineering functions to analyze, resolve, and eliminate customer complaints in medical device manufacturing.
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Sr. 供应商质量管理SQE（医疗） JabilShenzhen 12d Lead supplier quality system building and continuous improvement for medical injection molding and finished product suppliers to ensure product quality and compliance.
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Quality Manager – Medical Devices | Product Quality & Regulatory↗ Clarity MedicalCH, IN $800k–$800k12d Lead Product Quality, Quality Assurance, and QMS activities for medical electronic products including ECG, EMG, and Patient Monitoring Systems to ensure safety, reliability, and regulatory compliance.
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Quality Assurance and Regulatory Affairs Manager↗ Eli HealthRemote 12d Own the end-to-end Quality Management System (QMS) for a novel diagnostic device (Hormometer) to ensure FDA 21 CFR Part 820 compliance and support market launch.
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Quality Engineer (Manufacturing)↗ W. L. Gore & AssociatesFlagstaff, AZ, US 12d Provide technical support for commercialized medical device manufacturing, ensuring product quality, compliance, and process improvements.
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CSV/ MES Quality Validation↗ Thermo Fisher ScientificSt. Louis, MO, US 12d Ensure quality excellence and regulatory compliance across manufacturing operations by maintaining quality management systems, leading investigations, and driving continuous improvement.
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Reliability Engineer ResmedSingapore, Singapore 12d Improving reliability, availability, maintainability, and performance of manufacturing equipment, processes, and products for medical devices.
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Quality Assurance and Regulatory Affairs Manager EliRemote 12d Own the end-to-end Quality Management System (QMS) for a novel diagnostic device, ensuring FDA 21 CFR Part 820 compliance and supporting manufacturing and regulatory teams.
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Quality Manager - Private Label↗ L&r DistributorsRemote $110k–$110k13d Lead end-to-end quality system for private label beauty products ensuring consumer safety, regulatory compliance, and brand standards across cosmetics and OTC categories.
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Director of Quality Proton IntelligenceClayton, Victoria 14d Build, implement, and lead an ISO 13485-compliant quality management system for continuous potassium monitoring products advancing through clinical development and commercialization.
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Project Quality Engineer↗ AmbuCiudad Juárez, CHH, MX 15d Provide quality engineering support throughout the product lifecycle, ensuring compliance with quality, safety, and regulatory requirements for medical devices.
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Senior Quality Engineer - Product Development (m/f/d)↗ Hilo By AktiiaRemote 15d Senior Quality Engineer providing Design Assurance expertise and leadership in Design Controls, Risk Management, and Quality Systems for medical device product development.
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Quality Engineer I↗ Cirtec MedicalLowell, MA, US $80k–$85k15d Monitor and audit quality of manufactured medical devices, identify defect causes, and develop solutions.
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Quality Analyst↗ SterisMinneapolis, MN, US $76k–$76k15d Administer quality management systems to ensure adherence to ISO 9001, ISO 13485, FDA 21 CFR, EU GMPs, and other regulatory standards for medical device manufacturing.
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Intern - Quality Engineer - Oncology LabcorpBaltimore MD $37k–$37k15d Intern supporting the maintenance and improvement of risk management files, engineering change controls, and post-market surveillance data analysis for next-generation sequencing (NGS) medical devices.
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Quality Engineer I - Defined Term - 18 Months↗ Boston ScientificArden Hills, MN, US $72k–$72k15d Monitor, identify, investigate, and escalate product performance signals for urology capital equipment to improve patient outcomes.
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BD Quality Engineering Development Program Associate↗ BdFranklin Lakes, NJ, US 15d Rotational program for recent graduates to gain experience in Quality Engineering across New Product Development, Manufacturing Quality, and Post Market Quality over three years.
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Quality Systems Engineer↗ Katalyst Healthcares & Life SciencesIrvine, CA, US 15d Manage and execute CAPA and Nonconformance (NC) investigations, root-cause analysis, and corrective actions within a regulated medical-device environment.
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