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Healthcare
› Medical Device QA
Medical Device QA
1,115 open positions
Sr Design Quality Engineer
Bdx
USA GA - Covington BMD
16d
Senior Quality Engineer responsible for Design Control, Quality Assurance, and Document Control within a medical technology product line.
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Quality Engineer – Medical Devices
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Beecruit Pte Ltd
Singapore, Singapore
$42k–$60k
16d
Support daily quality and engineering activities for medical device manufacturing, including product/process investigations, root-cause analysis, and corrective actions.
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IMPROVEMENT TECHNICIAN
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Capgemini
Madrid, Community of Madrid, Spain
16d
Develop and apply engineering practice to define and execute quality management systems (QMS) for product and process quality, ensure compliance to standards, homologate products and processes, and register with competent authorities; manage Occupational…
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Quality Assurance Engineer
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Op Specialty Bracing
Kingston Upon Thames, England, UK
16d
Support international multisite integrated quality management system for pediatric medical device bracing.
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Complaint Manager (m/w/d), corpuls Kaufering (Hauswiesenstraße)
Corpuls
Kaufering, BAYERN
16d
Coordinate and lead quality meetings, systematically analyze error data, process customer feedback, and drive sustainable quality improvements for medical devices.
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Quality Complaint Analyst
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Outset Medical, Inc.
Tijuana, Baja California, Mexico
16d
Manage the full lifecycle of product complaints, from intake through investigation and closure, ensuring accurate documentation and timely reporting.
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Quality Manager - Medical Device QMS and Controlled Environments
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Celestica
Valencia, Valencian Community, Spain
16d
Lead alignment of ISO13485 QMS procedures with local facility operations, oversee cleanroom and factory production compliance, and manage environmental monitoring and sterilization for medical devices.
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Sr. Quality Engineer
Bdx
USA GA - Covington BMD
16d
Develop and maintain quality plans, procedures, and specifications to ensure compliance with regulatory requirements and industry standards for medical device products.
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Senior Quality Engineer
Medtronic
Salt Lake City, Utah, United States of America
$98k–$148k
16d
Lead process validation and quality system execution for manufacturing operations in a regulated medical device environment.
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Qualitätsmanager (m/w/d) X
N.O.C Engineering GmbH
Villingen-Schwenningen, BADEN_WUERTTEMBERG
16d
Managing the quality management system, including document control, audit preparation, CAPA handling, and customer complaint analysis.
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Ingeniero de Procesos
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Baxter
Ciudad de México, DIF, MX
16d
Ensuring storage and distribution documentation remains updated, accurate, and compliant with established standards.
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Senior Quality System Engineer (PAL)
Bostonscientific
Penang, Malaysia | N/A
16d
Ensuring compliance with FDA, ISO, cGMP, and MDR regulations through internal/external audits, CAPA management, and batch release analytical QA support for medical devices.
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Quality Engineer 1, EU MDR
Bdx
USA UT - Salt Lake City BAS
16d
Develops physical and functional test requirements, executes validation studies, and leads investigations to ensure medical device specifications and regulations (EU MDR) are met.
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Quality Engineer
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Nissha Medical Technologies
Buffalo, NY, US
$70k–$85k
16d
Ensure manufacturing processes comply with product specifications, customer requirements, and regulatory standards (ISO 9000, 13485, QSR) for medical devices.
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IMPROVEMENT TECHNICIAN
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Capgemini Engineering
Madrid, Community of Madrid, Spain
16d
Development and application of engineering practice to define and execute quality management systems (QMS), ensure compliance to standards, homologate products and processes, and register with competent authorities; management and audit of Occupational Health…
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Ingeniero de Procesos
Baxter
Tultitlan, Estado de México, MX
16d
Ensuring storage and distribution documentation remains updated, accurate, and compliant with established standards.
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Principal Manufacturing Engineer
Medtronic
Jacksonville, Florida, United States of America
$144k
16d
Coordinate and execute Verification and Validation (V&V) deliverables for supplier transfers within the Supplier Optimization group for medical devices.
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Senior Manager, Design Quality
Illumina
US - California - San Diego
$142k–$212k
16d
Leads Design Quality execution, risk management, and verification/validation for product-development programs in genomics.
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MITARBEITER*IN VIGILANZ & REKLAMATION (W/M/D), Potsdam - ROK
Christoph Miethke GmbH & Co. KG
Potsdam, BRANDENBURG
16d
Handling customer complaints and vigilance reports for neurosurgical implants to ensure product safety and quality.
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Senior Quality Engineer - Respiratory
Medline
Northfield, Illinois, US
$101k–$152k
16d
Set quality standards, validate processes, and manage supplier quality for medical device production to ensure compliance and product functionality.
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Global Quality Project Manager
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Galderma
Barcelona, Catalonia, Spain
17d
Coordinate a strategic, end-to-end Quality Management System (QMS) transformation to simplify, harmonize, and digitalize quality operations globally.
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Directeur de la qualité/Directrice de la qualité
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Puzzle Medical Devices® Inc.
Montreal, Quebec, Canada
17d
Strategic leadership and oversight of the company's Quality function, ensuring product and process quality, regulatory compliance, and risk management within the medical device industry.
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Lead Design Control Engineer
Gehc
Haifa, IL
17d
Manage quality systems, processes, and procedures to assure product safety, quality, and site compliance for the Haifa PoC Ultrasound business.
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Senior Quality Systems Specialist
Russell Tobin
Singapore
18d
Lead implementation, maintenance, and continuous improvement of Quality Management Systems (QMS) for medical devices, ensuring compliance with ISO 13485 and Singapore HSA regulations.
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CQ/RA Specialist BeNeLux
Johnson and Johnson
België
€63k–€98k
18d
Support and maintain the Quality Management System (QMS) for MedTech businesses in Belgium and Luxembourg, ensuring compliance with quality requirements and regulatory expectations.
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Senior Quality Engineer - Metrology and Calibration
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Biopharma Consulting Jad Group
Houston, TX, US
18d
Lead the remediation of a calibration program at a regulated manufacturing facility to ensure compliance with internal, customer, and regulatory audits.
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Quality Engineer - Temporal 1 año
↗
Bd
Reynosa, TAM, MX
18d
Lead product and process transfers, manage quality documentation, and ensure GMP/ISO compliance for medical device manufacturing.
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Especialista Projeto Qualidade
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Bd
Juiz de Fora, Minas Gerais, Brazil
18d
Leading project requirements gathering, planning, technical management, and monitoring of performance indicators for medical technology projects.
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Sr Spec Quality Process
Medline
Northfield, Illinois, US
$92k–$138k
19d
Design, integrate, and maintain global quality processes, complaint management, device vigilance, and regulatory reporting systems for medical devices, pharmaceuticals, and biologics.
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Systems Engineer
Insulet
Acton, Massachusetts, US
$82k–$123k
19d
Design, development, sustaining, and quality processes for wearable medical devices (insulin pumps) used by patients globally.
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Quality Engineer I
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Cirtec Medical
Rock Hill, SC, US
19d
Monitor and audit quality of manufactured medical devices, analyze root causes of non-conformances, and implement corrective actions.
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Engineer III, Quality
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Meso Scale Diagnostics
MD, US
$101k–$155k
19d
Subject matter expert for planning and directing quality standards, processes, materials, and products in accordance with company Quality System programs, plans, SOPs, and policies.
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Principal Software Quality Engineer, SaMD and Cybersecurity
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Nanthealth
Remote
19d
Provide technical leadership and independent quality oversight of software development, cybersecurity, verification, validation, and release activities for Software as a Medical Device (SaMD) and connected medical device software products.
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Senior Quality Design Engineer
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Boston Scientific
Galway, County Galway, Ireland
19d
Ensure patient safety and product excellence by leading design assurance, risk management, and lifecycle quality activities for new and commercialized medical devices.
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Mitarbeiter für Qualitätssicherung/ Regulatory Affairs Onsite (w/m/d)
Peter Pflugbeil GmbH
Zorneding, BAYERN
19d
Quality Assurance and Regulatory Affairs specialist for medical devices, responsible for documentation, quality management, product testing, and supplier management.
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Mitarbeiter für Qualitätssicherung / Regulatory Affairs Onsite (w/m/d)
Peter Pflugbeil GmbH
Zorneding, BAYERN
19d
Quality Assurance and Regulatory Affairs specialist ensuring compliance and documentation for a medical device manufacturer's product portfolio.
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Principal Engineer, S/W QA Cyber Security
Bostonscientific
Gurgaon IN-HR, India | N/A
19d
Senior individual contributor providing independent Quality oversight and technical leadership for product cybersecurity activities across the medical-device product lifecycle.
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CAPA Leader, Regional Quality PDx
Gehc
Amersham, GB
19d
Lead the effective closure of CAPA/Deviation/Change Control records and drive high-quality QMS outcomes across the PDx network.
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Quality Engineer III
Jabil
Gurnee, IL, US
$83k–$150k
19d
Leads development and implementation of quality plans, programs, and procedures using quality control statistics and lean manufacturing concepts to ensure product quality conforms to company, customer, and regulatory requirements.
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Senior Design Quality Engineer (Mechanical)
Stryker
Portage, Michigan, US
$78k–$130k
19d
Execute and own quality engineering activities for mechanical workstreams in new product development, ensuring safety, reliability, and manufacturability of medical devices.
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Senior Design Quality Engineer (Software/Electrical)
Stryker
Portage, Michigan, US
$78k–$130k
19d
Provide quality support for new product development of software and electrical medical devices, partnering with cross-functional teams on design verification, validation, risk management, and cybersecurity.
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Quality Systems Specialist
Baxter
St Paul, Minnesota, US
$88k–$121k
19d
Ensure the quality, safety, and reliability of medical device products by managing change controls, investigations, audits, and product disposition.
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Quality Manager
Ttp
Cambridge, England, gb
20d
Own and improve the Quality Management System (QMS) for complex bioprocess equipment and automation systems, ensuring compliance with ISO 9001 and regulatory standards from development through customer delivery.
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Directeur de qualité et de la gestion des risques F/H
SCM ICB DIJON
Dijon, Côte-d'Or
20d
Lead the quality management system, risk management, and HAS certification across three cancer treatment sites.
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Director of Quality
Ketryx
Boston
$150k–$185k
20d
Own the Quality Management System (QMS), Information Security Management System (ISMS), and AI governance program for a compliance software company serving regulated industries.
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Quality Manager
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Sparrow Search
Glenview, IL, US
$80k–$90k
20d
Lead the Quality Management System (QMS) for a medical device manufacturing company, ensuring compliance with FDA and ISO 13485 standards.
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Sr Quality Engineer I - Manufacturing
↗
Tandem Diabetes Care, Inc.
San Diego, CA, US
$110k–$121k
20d
Senior Quality Engineer providing quality guidance, risk reduction, and compliance assurance for medical device manufacturing and sustaining engineering.
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Metrology Engineer
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Velosity
Brooklyn Park, MN, US
$75k–$100k
20d
Develop, implement, and maintain metrology systems and processes to ensure dimensional accuracy and compliance with medical device standards for complex components.
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Senior Manager, Quality Assurance
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Veranex
Providence, RI, US
20d
Lead the quality assurance team to ensure compliance with FDA regulations and industry standards for MedTech development products.
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Teamleiter Qualitätsplanung / Qualitätsmanagement – Medizintechnik & CAQ-Systeme (m/w/d)
AllatNet Recruiting GmbH & Co. KG
Ravensburg, Württemberg, BADEN_WUERTTEMBERG
20d
Leading the Quality Planning team to optimize quality processes, manage resources, and ensure compliance with regulatory standards in the medical device industry.
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