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Healthcare
› Medical Device QA
Medical Device QA
1,119 open positions
Senior Quality Assurance Engineer II
Merit
Pearland, TX, US
27d
Ensures product quality and compliance for medical devices through risk management, supplier audits, nonconformance analysis, and quality system maintenance.
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Engineer 2, Quality Engineering
Smithnephew
MYS - Penang, MY
27d
Ensures quality, reliability, and compliance of medical devices and manufacturing processes throughout the product lifecycle.
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Senior Quality Assurance Specialist
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Siemens Healthineers
Ottawa, ON, CA
$73k–$105k
27d
Leads CAPA activities, supports QMS and site Quality Operations, and drives quality governance and improvement in a regulated medical device/pharma environment.
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Assistenz / Assistent Qualitätsmanagement (w/m/d), Julius Zorn GmbH
Julius Zorn GmbH
Aichach an der Paar, BAYERN
27d
Supporting the maintenance and development of the Quality Management System (QMS) for a medical device manufacturer, ensuring compliance with ISO 13485 and regulatory requirements.
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Quality Engineer
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Qcs Staffing
Sligo, County Sligo, Ireland
27d
Coordinating Quality System elements, auditing systems, managing CAPA, and investigating customer complaints in a highly regulated manufacturing environment.
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Sr. Quality Director
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Flex
Guadalajara, Jalisco, Mexico
27d
Develop, implement, and coordinate product assurance programs to prevent or eliminate defects in new or existing products for manufacturing and design locations.
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Director de Aseguramiento de Calidad y Asuntos Regulatorios
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Kuehne+Nagel
Cuautitlán Izcalli, México, Mexico
27d
Define and lead the national Quality Assurance and Regulatory Affairs strategy to protect operating license, ensure legal/regulatory/corporate/contractual compliance, and ensure reliable services in Healthcare and Semiconductors.
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Vice President, Global Quality Assurance, Medical Devices & Surgery
Baxter
Deerfield, Illinois, US
$280k
27d
Lead global quality strategy, systems, and compliance for three medical device businesses from development through post-market use.
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Senior Associate II, Quality Audits
Biibhr
Research Triangle Park, NC, US
$93k
27d
Conduct risk-based internal and supplier audits to ensure compliance with ISO 13485 and GxP regulatory frameworks (FDA, EMA) for the Regional Americas.
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Quality Engineer
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Bvi Medical
Warwickshire, England, UK
27d
Execute customer complaint investigations, manage non-conformance (NC) and Corrective and Preventive Action (CAPA) processes, and support Engineering Change Orders (ECOs) to ensure regulatory compliance and product quality in a medical device environment.
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Quality Systems Specialist
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Essity
Reynosa, Tamaulipas, Mexico
27d
Create and administer technical documentation for manufactured products, manage QMS compliance, and act as the liaison for product change approvals between Reynosa and the US Legal Manufacturer.
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Quality Engineer
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Medline Industries
Mundelein, IL, US
$79k–$119k
27d
Manage post-market quality activities including complaint investigations, surveillance data analysis, and CAPA initiatives to ensure medical device compliance and safety.
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Mitarbeiter:in (m/w/d) im Qualitätsmanagement (Sachbearbeitung - in Teilzeit)
Holthaus Medical GmbH & Co.KG
Remscheid, NORDRHEIN_WESTFALEN
27d
Ensuring high quality standards for medical products and processes through documentation management, specification verification, and supplier compliance checks.
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Manufacturing Quality & Technical Manager
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Amcor
Commerce, CA, US
27d
Lead quality systems and technical compliance for a medical device manufacturing plant, ensuring product safety and regulatory adherence.
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Senior Quality Engineer
Abbott
United States - California - Pomona
$90k–$180k
27d
Senior Supplier Quality Engineer driving continuous process improvement, compliance, and risk management for IVD medical devices and diagnostics.
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Senior Quality Officer
Eurofins
Dublin 18, ie
28d
Maintain the Quality Management System (QMS) for a clinical diagnostic laboratory, ensuring compliance with ISO 15189 and ISO 9001 standards while supporting continuous improvement initiatives.
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Digital Quality & GxP Manager
Careaccess
Remote
$110k
28d
Manage compliance risk and provide practical guidance on GxP quality across the software product lifecycle, including internal and external software products, systems, and AI products.
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Specjalista / Specjalistka ds. zapewnienia jakości
Grafton
Warszawa, mazowieckie
28d
Developing, verifying, and evaluating procedures and documentation for an Integrated Quality Management System within a healthcare organization.
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Quality Engineer I or II
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Smc
Santa Rosa, CA, US
$75k
28d
Support SMC's quality system by leading new product launches, managing inspection methods, troubleshooting quality issues, and driving continuous improvement in a medical device manufacturing environment.
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Principal Quality Systems Engineer - Cardiac Rhythm Management & Diagnostics (CRMDx)
Bostonscientific
Arden Hills US-MN, United States | N/A
28d
Design Control representative leading awareness, visibility, and communication of quality initiatives in support of global and CRM quality goals, ensuring compliance of the CRM Design Control to BSC Global Quality System and applicable regulatory requirements.
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Sr Software QA Engineer
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Dexcom
KA, IN
28d
Sr Software QA Engineer providing technical guidance on software design assurance, compliance with medical device regulations, and risk management for continuous glucose monitoring (CGM) products.
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Quality Engineer
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Zavation Medical Products
Flowood, MS, US
28d
Support manufacturing and quality departments to ensure compliance with industry and regulatory standards, including GMP, ISO, and FDA requirements.
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Project Quality Manager (m/w/d)
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Gerresheimer
Bünde, NW, DE
28d
Coordinate quality activities across the entire product development lifecycle and support international production sites in achieving successful series production.
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Software QA Engineer 1
Dexcom
Bengaluru, India
28d
Ensure conformance to software development processes and safety/quality regulations (IEC 62304, ISO 13485) for medical device software.
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Senior Quality Engineer
Tempus
Chicago, US
$90k
28d
Lead verification, validation, and maintenance of host systems supporting Tempus Medical Devices and AI applications to ensure regulatory compliance and clinical safety.
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Senior Design Quality Engineer - Cardiac Rhythm Management & Diagnostics (CRMDx)
Bostonscientific
Arden Hills US-MN, United States | N/A
28d
Senior Design Quality Engineer supporting active implantable medical devices, ensuring product safety, quality, and regulatory compliance throughout the lifecycle.
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Group Manager Quality
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Raysearch Laboratories
Stockholm, Stockholm County, Sweden
28d
Lead the Quality function and a team of three to evolve the QMS into a lean, scalable system for a medical device company, focusing on AI/ML compliance and regulatory standards.
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Senior Quality Systems Engineer
Bostonscientific
Arden Hills US-MN, United States | US-MN-Arden Hills, US-MN-Maple Grove, US-MA-Marlborough
28d
Senior Quality Systems Engineer leading material controls processes, supplier quality, and regulatory compliance for medical devices.
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Quality Engineer
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Bihler of America
Phillipsburg, NJ, US
28d
Supports the effective implementation and maintenance of the Quality Management System for the design, development, manufacture, and distribution of medical devices.
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Quality Engineer
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Charter Medical, LLC
Winston-Salem, NC, US
28d
Ensures the successful performance of the company's Quality Management System in support of FDA 21 CFR Parts 210, 211, 820 and ISO 13485:2016.
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Quality Engineer
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Hero Recruitment
Athlone, Ireland
28d
Maintain and continuously improve the Quality Management System (QMS) for FDA-regulated medical device manufacturing, ensuring compliance with ISO 13485 and supporting cross-functional teams.
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Quality Compliance Engineer
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Rhythmlink International, LLC
Columbia, SC, US
28d
Maintain and improve the Quality Management System (QMS) and ensure compliance with regulatory requirements while owning the Supplier Management program.
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Quality Engineer II
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Fresenius Medical Care
Bogotá, CUN, CO
28d
Responsible for quality planning, internal audits, data collection, specification development, design review, qualification, and risk management to ensure compliant medical devices.
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Sr. Quality Director
Flextronics
Mexico, Guadalajara
28d
Develop, implement, and coordinate product assurance programs to prevent or eliminate defects in new or existing products for manufacturing and design locations across the Americas, Europe, and Asia.
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Senior Associate Specialist,Quality
Gehc
IND19-01-Bengaluru-EPIP 122 (Phase II), IN
28d
Develop and maintain systems, rules, and processes to ensure fulfillment of internal and external requirements and meet specified standards for products and projects.
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Quality Engineer
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American Orthodontics
Sheboygan, WI, US
28d
Lead investigations of quality issues, manage Corrective and Preventative Action (CAPA) activities, and analyze quality data to drive product and process improvements.
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Quality Engineering Specialist (On SIte)
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Myant Shared Service Corp.
Mississauga, ON, CA
28d
Hands-on quality engineering specialist ensuring compliance and process control in medical device manufacturing, from design transfer through production and supplier quality.
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Praktikant (m/w/d) Quality Management & Regulatory Affairs
Adeor
DE-83626 Valley
29d
Support Quality Management and Regulatory Affairs teams with a focus on ERP system development and digital transformation processes.
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Ingénieur Qualité Expérimenté - Design Control F/H (CDD 6 mois)
Corwave
Clichy, Nanterre
29d
Ensure regulatory compliance of Verification & Validation (V&V) activities for medical devices throughout the product lifecycle.
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Responsable/Coordinateur Qualité Série F/H
EMI SAS - ETUDE MOULE INJECTION
Braud-et-Saint-Louis, L'Estuaire
29d
Managing the series quality team and ensuring product conformity in manufacturing workshops.
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Senior Specialist Kwaliteit & Risicobeheersing
Levanto Groep
Sittard, Sittard-Geleen
€55k–€71k
29d
Developing and anchoring the quality management system (ISO 9001) and integral control framework, linking quality with risk management and compliance in mental health care.
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Mitarbeiter für Etikettendruck (m/w/d) Vollzeit
Eurofins
Birkenfeld, BW, de
29d
Ensuring label quality, documentation, and production coordination for medical device labeling.
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Quality Validation Specialist
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Advanced Medical Solutions
Plymouth, England, UK
29d
Own the site-level validation process and ensure quality engineering tasks are completed to support medical device manufacturing and regulatory compliance.
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Tijuana - Engineer II - Applications*
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Integer
Tijuana, BCN, MX
29d
Engineer II responsible for evaluating, selecting, and applying engineering techniques to develop, document, and implement new product and process technologies of moderate complexity, while ensuring adherence to Quality Management Systems (QMS) and FDA…
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Senior/Quality Engineer (Medical Device Manufacturing) / East
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Recruitpedia Pte. Ltd.
Singapore, S00, SG
29d
Support quality activities across manufacturing processes, products, and daily operations in a medical device manufacturing environment.
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Tijuana - Engineer II - Applications*
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Integer
Tijuana, BCN, MX
29d
Engineer II responsible for evaluating, selecting, and applying engineering techniques to develop, document, and implement new product and process technologies of moderate complexity, while ensuring adherence to Quality Management Systems (QMS) and…
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Sr. Quality Engineer
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Warsaw, IN, US
29d
Sr. Quality Engineer leading manufacturing inspection plans, validation, NPI transfers, CAPA investigations, and supplier quality management to ensure product compliance and reliability.
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Sr. Quality Engineer
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Maverick Tech
Warsaw, IN, US
29d
Lead quality engineering in manufacturing to ensure product compliance, drive continuous improvement, and manage risk across the product lifecycle.
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Sr Engineer Quality
Medline
Chicago, Illinois, US
$101k
29d
Setting quality standards, managing process control and validation, and leading supplier quality programs for medical device manufacturing.
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Quality Engineer - Capital Equipment & Furnishings
Medline
Chicago, Illinois, US
$79k
29d
Set quality standards, validate processes, and manage supplier quality for medical device capital equipment and furnishings.
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