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Healthcare
› Medical Device QA
Medical Device QA
1,115 open positions
Technical Quality Engineer
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Putnam Plastics Corporation
Dayville, CT, US
20d
Uses quality and process engineering principles to investigate, analyze, develop, and optimize manufacturing processes for medical device components to ensure compliance and product quality.
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Senior Quality RI FG Engineer
Bostonscientific
Penang, Malaysia | N/A
20d
Senior Quality Engineer responsible for product release decisions, root cause analysis of defects, and validation of processes and equipment in a regulated medical device manufacturing environment.
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CAPA Leader
Gehc
Chalfont St Giles, GB
20d
Lead the effective closure of CAPA/Deviation/Change Control records across sites/departments in the PDx network using project management and Lean methodologies.
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Quality Item Master Data Specialist (m/w/d)
Medline
Kleve, DE
20d
Central interface between product master data and physical warehouse reality, ensuring packaging, labeling, and product information are accurate, complete, and compliant.
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Senior Quality Engineer
Bdx
USA CA – Brea
$106k–$169k
20d
Senior Quality Engineer supporting new product development and maintenance for medical devices, ensuring compliance with design control and regulatory requirements.
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Staff Design Quality Engineer
Stryker
Waltham, Massachusetts, US
$93k–$155k
20d
Staff Design Quality Engineer supporting new product development and quality activities throughout the medical device product lifecycle.
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Sr. Quality Engineer, Failure Analysis
Bdx
USA CA - Irvine Laguna Canyon
$106k–$169k
20d
Lead failure analysis investigations on returned medical devices and manufacturing nonconformances to identify root causes and validate failure mechanisms.
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Manager Quality Systems (w/m/d)
NDI Europe GmbH
Radolfzell am Bodensee, BADEN_WUERTTEMBERG
20d
Lead the Quality Engineering team and drive the continuous improvement of the Quality Management System (QMS) for a medical device company specializing in 3D-tracking technology.
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Quality Management System/CAPA Specialist
Philips
Bothell, Washington, United States
$102k–$164k
20d
Facilitate the CAPA process and support Audit Readiness activities to ensure an efficient and compliant Quality Management System (QMS) in a highly regulated environment.
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Responsable Qualité et Projets Groupe H/F
OUEST PATHOLOGIE
Ille-et-Vilaine, Bretagne
21d
Pilot the group-wide quality strategy, accreditation, and risk compliance for an anatomocytology group, while coordinating cross-functional projects and managing site quality managers.
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COOK Medical Summer 2027 R&D Engineering Co-Op
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Cook Group
Bloomington, IN, US
21d
12-week paid summer internship in Research and Development Engineering for medical device manufacturing.
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Project Engineer III – Labeling Projects (2622)
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Medchem Engineering Services
Añasco, PR, US
$79k–$87k
21d
Lead and execute labeling update projects in a regulated medical device manufacturing environment, ensuring compliance with quality and regulatory requirements.
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Product Engineer (Medical Devices)
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Recruit Expert Pte. Ltd.
Outram, S00, SG
21d
Manage product sustaining engineering, design changes, verification, testing, and root cause investigations to ensure compliance with medical device regulatory standards and customer specifications.
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Quality Engineer
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Golden West Biosolutions, LLC
Temecula, CA, US
$75k–$95k
21d
Implement, maintain, and improve a unified Quality Management System (QMS) for biological materials and diagnostic manufacturing.
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Quality Engineer 2
Smithnephew
US - Maple Plain
$74k–$112k
21d
Lead investigations into manufacturing and product quality events, execute quality objectives for product performance and compliance, and provide hands-on support for sterile packaging and sterilization processes in a medical device manufacturing environment.
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Senior Quality Systems Specialist
Stryker
Redmond, Washington, US
$83k–$139k
21d
Ensure effectiveness of quality management system by driving compliance, leading problem-solving efforts, and partnering with cross-functional teams to resolve quality issues.
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Quality Engineer I
Bdx
USA IL - Carol Stream
21d
Ensures compliance with FDA QMSR, ISO 13485, and EU MDR regulations through quality system procedures, investigations, and validation activities for medical device products.
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Complaint Coordinator (m/w/d) Post Market Quality
Stryker
Freiburg, Germany
€45k–€75k
21d
Handling field complaints and supporting error analysis for post-market surveillance of medical devices.
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Design Quality Engineer
Smithnephew
Austin, TX, US
21d
Design Quality Engineer supporting the ENT New Product Development team to bring safe, reliable medical device technologies from concept through development.
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Verkaufssachbearbeiter/in
1zu1scale GmbH Prototypen
Dornbirn, VORARLBERG
21d
Ensuring and continuously developing quality standards and processes in a regulated environment.
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Quality Engineer
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Autocam Medical
Murfreesboro, TN, US
21d
Ensuring precision and quality in medical parts inspection, driving root cause analysis, and supporting continuous quality improvement.
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Principal Quality Design Assurance Engineer
Saluda Medical
Macquarie Park, New South Wales
21d
Senior Quality Engineering role defining, driving, and improving new product development, sustaining engineering, and post-market activities for a closed-loop neuromodulation platform.
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Design Quality Engineer II
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Verathon
Burnaby, BC, CA
$81k–$108k
22d
Ensure quality standards and compliance throughout the product lifecycle for medical devices, from new product development to sustaining engineering.
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Senior Quality Manager
Baxter
Monterrey, Nuevo León, MX
22d
Strategic and operational leadership for the Quality organization, ensuring patient safety, regulatory compliance, and continuous improvement across the product lifecycle.
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Senior, Software Design Quality Engineer
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React Health
Remote
22d
Ensure design quality and regulatory compliance for commercialized medical device software products, including risk management and validation.
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Quality Engineer I
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Integer
Hudson, MA, US
$64k–$93k
22d
Support quality activities for a high-volume hydrophobic coating plant, ensuring compliance with FDA regulations and quality management systems.
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Global Regulatory Compliance Director
Bostonscientific
Marlborough US-MA, United States | US-MN-Arden Hills
22d
Provide strategic leadership, governance, and stewardship of the global internal audit team and process for the Global Quality Systems group.
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Sr. Reliability Engineer (Stapling Portfolio / Surgical)
Medtronic
North Haven, Connecticut, United States of America
22d
Lead reliability engineering for advanced surgical stapling systems, investigating failure mechanisms and driving product improvements to ensure quality and patient safety.
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Platform Quality Assurance Leader - Personal Health Care-1
Pg
MASON BUS AND INNOVATION CTR, US
$91k–$117k
22d
Provide QA leadership for GMP product quality systems and activities across the Personal Health Care business category for Respiratory and Sleep Franchise new product initiatives.
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Quality Engineer
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Nelipak
Phoenix, AZ, US
$70k–$90k
22d
Establish material, process, and product quality standards, specifications, and manufacturing methods for medical packaging while ensuring compliance to ISO 13485.
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Customer Advocacy Generalist
Dexcom
Vilnius, Lithuania
€19k–€24k
22d
Review and evaluate customer complaints, maintain cGMP documentation, and support Medical Device Reporting and corrective/preventive actions for a continuous glucose monitoring device.
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Quality Systems Engineer
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Span America Medical Systems, Inc
Maryland Heights, MO, US
22d
Define, implement, and maintain effective Quality Systems ensuring compliance with FDA Quality Systems Regulation, ISO 13485, and other applicable regulations for medical devices.
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Quality Engineer I
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Cirtec Medical
Sturtevant, WI, US
$78k–$94k
22d
Monitor and audit quality of manufactured medical devices, find defect causes, and develop solutions.
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Senior Quality Engineer
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Laborie Medical Technologies
Portsmouth, NH, US
22d
Senior Quality Engineer ensuring technical regulatory and quality requirements are met within the Quality Management System and throughout the product life cycle for medical devices.
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Quality Officer
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Medical Support Offshore Ltd
Southampton, ENG, GB
22d
Support the Quality Management System, ensure compliance, and drive continuous improvement across a global medical support organization.
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Quality Assurance Manager
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Si-Bone
Santa Clara, CA, US
$141k–$155k
22d
Manage the quality control group for inspection, release, and compliance of medical implants and instruments.
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Document Control Specialist 3 - Evening Shift
Dexcom
Athenry, Ireland
€41k–€53k
22d
Manage the change control system, review and release change orders, and maintain quality documents and records in compliance with ISO 13485 and 21 CFR Part 820.
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Senior Engineer, Quality Assurance
Stryker
Michigan, Portage 3800 East Centre Ave, US
$82k–$136k
22d
Lead Emergency Care critical investigations and drive improvements for medical technology product safety and performance.
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Quality Assurance Manager
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Koya Medical
Dallas, TX, US
22d
Oversees the Quality Management System (QMS) to ensure regulatory compliance and operational effectiveness for medical device manufacturing.
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Quality Associate III
Baxter
Skaneateles, NY, US
$96k–$132k
22d
Own and manage assigned Quality Management System (QMS) processes supporting U.S. depot operations, serving as the primary Quality partner for process performance, compliance, risk identification, and continuous improvement.
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Engineering Manager, Post Market Quality
Stryker
Tempe, Arizona, US
$118k–$197k
22d
Lead global post-market quality systems, failure analysis, complaint handling, and regulatory reporting for medical devices.
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Senior Engineer, Advanced Quality
Stryker
Carrigtwohill, Ireland
€47k–€77k
22d
Senior Quality Engineer driving reliability, human factors, risk management, and design validation for new medical device development to ensure regulatory compliance and safe product launch.
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ABTEILUNGSLEITUNG QUALITY MANAGEMENT SYSTEM (W/M/D), Potsdam - ROK
Christoph Miethke GmbH & Co. KG
Potsdam, BRANDENBURG
22d
Leading the Quality Management System (QMS) department and driving the evolution of a scalable, digital quality management system for a medical device manufacturer.
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Senior Quality Engineer – Medical Device Manufacturing
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Mgd Industrial Corp.
Humacao, PR, US
$76k–$81k
22d
Senior Quality Engineer supporting manufacturing operations, ensuring product quality, process reliability, and regulatory compliance in medical device production.
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Quality Manager
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Mirion
Oak Ridge, TN, US
22d
Oversee compliance activities for the organization's Quality and Safety Management systems, ensuring adherence to local, state, and government regulations.
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Quality Systems Engineer
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Siemens Healthineers
Austin, TX, US
$96k–$133k
22d
Primary quality engineering resource supporting manufacturing operations, incoming inspection, supplier quality, and quality systems in an ISO 13485:2016-compliant environment.
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Quality Engineer I - Evening shift
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Medtronic
Galway, County Galway, Ireland
€42k
22d
Develops, modifies, applies and maintains quality standards and protocol for releasing finished sterilised product under supervision.
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Junior Executive QA
Meril
Daman, Daman and Diu
23d
Ensure compliance with USFDA, GMP, and ISO 13485 requirements in the medical device/pharmaceutical industry.
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Sr. Quality Engineer
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Tecomet
Wilmington, MA, US
23d
Ensuring compliance with internal and external customer requirements through quality engineering, continuous improvement, and adherence to FDA/ISO regulations within medical device manufacturing.
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Engineer II, Device Quality
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Mannkind Corporation
Danbury, CT, US
23d
Support medical device quality and risk management activities for existing and new products throughout the product lifecycle.
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