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Healthcare
› Medical Device QA
Medical Device QA
631 open positions
Senior Engineer, NPD Quality
Edwards
USA - California – Irvine
$108k–$153k
5d
Principal Quality Engineer leading quality engineering support and leadership for New Product Development (NPD) of transcatheter heart valves, ensuring compliance with regulatory requirements and overseeing design and development processes.
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Quality Specialist
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Steripro International
Greater Sudbury, ON, CA
$65k–$65k
5d
Support and strengthen quality, compliance, and continuous improvement activities in a regulated healthcare-related operational environment, specifically within the Medical Device Reprocessing Department.
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Senior Engineer, Manufacturing QA
Edwards
USA - California – Irvine
$108k–$153k
5d
Senior Engineer ensuring manufacturing quality compliance, optimizing production processes, and managing risk for medical device development and distribution.
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Senior Quality Engineer
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Guardant Health
Redwood City, CA, US
$97k–$97k
5d
Ensures quality compliance for IVD product development and operations in a regulated environment, managing risk, validation, and supplier programs.
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Quality Engineer
Gehc
Haifa HEALTHCARE HA IL 2
5d
Develop and maintain systems, rules, and processes to ensure fulfillment of internal and external requirements and regulatory compliance for healthcare products.
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Quality Associate II - Onsite Weekdays
Baxter
Medina, New York, US
5d
Ensuring compliance with medical device regulations and corporate processes, managing audits, and overseeing quality management systems.
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Analista de inspeccion recibo
Cardinalhealth
Mexico-Juarez Presource
5d
Develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications.
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QMS Specialist
Philips
Latham, New York, United States
$63k–$63k
5d
Ensure compliance with legal, regulatory, and international standards for the Quality Management System (QMS) through documentation, process improvement, and controlled execution of procedures.
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Senior Engineer, Quality
Edwards
USA - California – Irvine
$108k–$108k
5d
Senior Quality Engineer applying quality engineering principles to maintain compliant manufacturing processes, resolve complex product quality and compliance issues, and drive continuous improvement in a regulated medical device environment.
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Quality Engineer - Advanced Wound Care
Medline
Northfield, Illinois, US
$79k–$79k
5d
Independently set quality standards, develop testing methods, and manage vendor quality for advanced wound care medical devices.
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Senior Software Quality Engineer
Medtronic
London, London, United Kingdom
$77k–$77k
5d
Ensure software safety, reliability, and compliance throughout the medical device product development lifecycle.
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Sr Quality Engineer
Medtronic
Juncos, Puerto Rico, United States of America
5d
Provide quality leadership and oversight for manufacturing daily activities, ensuring products and processes meet regulatory and business requirements.
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Quality Manager
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DuPont
Minneapolis, MN, US
$100k–$100k
5d
Coordinate the development and administration of the company's quality assurance (QA) system, establish quality policies, and lead internal audits to support ISO and other registrations.
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Manager, Quality Engineering
Novanta
Irvine, CA, US
$110k–$180k
5d
Lead quality engineering activities including design control, risk management, validation, and regulatory compliance for engineered components and sub-systems in healthcare and advanced manufacturing.
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Senior Design Quality Engineer
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Irhythm Technologies
Cypress, CA, US
$138k–$138k
5d
Senior Design Quality Engineer ensuring medical device products meet quality standards, design controls, and regulatory requirements from concept through commercialization.
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Quality Engineer
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Katalyst Healthcares & Life Sciences
Chicago, IL, US
5d
Ensure compliance with FDA, ISO, and other regulatory standards while managing manufacturing quality operations and supporting the production lifecycle.
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Senior Quality Engineer - Process Validation
Medtronic
Athlone, County Westmeath, Ireland
$65k–$65k
5d
Lead end-to-end validation activities for medical devices to ensure processes, equipment, and products meet regulatory and quality standards throughout the product lifecycle.
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Quality Engineer II - Process Validation
Medtronic
Athlone, County Westmeath, Ireland
$50k–$50k
5d
Senior Quality Engineer supporting end-to-end process validation for medical device new product introductions and lifecycle management.
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Staff Quality Engineer
Stryker
Kalamazoo, Michigan, US
$89k–$89k
5d
Drive product and process quality compliance across manufacturing operations for medical instruments, leading investigations, continuous improvement, and new product introductions.
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QA Engineer - PFT (12-Month Contract)
Resmed
Johor Bahru, Malaysia
5d
Support manufacturing operations to achieve quality, availability, and value objectives through Quality Engineering methods, validation, and risk management.
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Sr. Quality Management System Specialist
Stryker
Portage, Michigan, US
$73k–$73k
5d
Design, maintain, and continuously improve a quality management system to support regulatory approval and business growth for global medical device markets.
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Manager, Quality Engineering
Stryker
Mahwah, New Jersey, US
$142k–$142k
5d
Lead quality assurance activities to ensure product quality, process performance, audit readiness, and continuous improvement across site operations.
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Senior Supplier Quality Engineer
Philips
Colorado Springs, Colorado, United States
$92k–$92k
5d
Ensures supplier quality, compliance, and process capability for Image Guided Therapy Devices across sustaining activities.
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Supervisor- Quality Systems (Documentation Center)
AbbVie
Heredia, Heredia Province, cr
5d
Supervise the Document Control Department in Costa Rica to ensure efficient, consistent operation aligned with corporate standards and regulatory requirements, managing controlled documentation for medical products.
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Senior Quality Engineer- Design Quality – Lifecycle Management
AbbVie
North Chicago, IL, us
6d
Ensure medical device products are properly transferred from development to manufacturing and maintained on market while assuring compliance to local, divisional, and corporate policies and external agency regulations worldwide.
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Quality Management Systems Specialist
Jobgether
Remote
6d
Operational backbone of a regulated Quality Management System (QMS) for software-focused medical devices, ensuring ISO 13485 compliance and driving CAPA, NCR, document control, and audit readiness.
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Product Quality Engineer
Philips
Bangalore, IN
6d
Lead design controls, quality management, and risk integration for medical device development, transfer, and sustaining initiatives.
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Quality Assurance Technical Specialist (Technical Leader- Tuas Avenue 2)
↗
Bd
Tuas, S00, SG
6d
Lead technical quality initiatives, drive investigations for non-conformances and customer complaints, and ensure compliance with regulatory requirements for MedTech products.
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New Product Development Senior Supplier Quality Engineer
Medtronic
North Haven, Connecticut, United States of America
6d
Senior Supplier Quality Engineer ensuring design transfer and manufacturability for new medical device products by managing supplier selection, qualification, and process validation.
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Senior Staff QE
Stryker
Cork, Ireland
$62k–$62k
6d
Define and execute validation strategies for medical devices, ensuring regulatory compliance and establishing industry best practices across multiple sites.
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Quality Engineer
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Ametek
Mansfield, MA, US
$70k–$90k
6d
Create and maintain Quality Assurance functions, procedures, and practices to ensure quality issues are identified, documented, tracked, and resolved within a medical device manufacturing environment.
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Production QA Eng
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North American Production Sharing
Tijuana, BCN, MX
6d
Evaluate, investigate, and maintain Quality Systems at the Tijuana facility, including Nonconforming Material Reports, Manufacturing Deviations, Change Control, CAPA, and Part Number Generation.
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Director of Quality Assurance
CoMind
London, UK
6d
Lead the Quality function for a non-invasive neuromonitoring medical device, covering QMS, design quality assurance, and supplier quality to ensure compliance and readiness for market release.
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Sustaining Quality Director
Medline
Northfield, Illinois, US
$177k–$177k
6d
Provide leadership and direction to the Sustaining Quality organization to ensure quality and compliance for commercial products and associated Quality Management System processes.
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Director, Product & Commercial Quality
Kenvue
North America, United States, New Jersey, Summit
$191k–$191k
6d
End-to-end quality leadership for Skin Health products, overseeing Regional Product Quality, Commercial Quality, R&D Quality & Compliance, and Product Lifecycle Management.
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Sr Engineer Quality
Medline
Northfield, Illinois, US
$101k–$101k
6d
Establish quality standards, validate processes, and manage supplier quality for medical device manufacturing and regulatory compliance.
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Senior Quality Engineer - Complaints Handling
Stryker
Gurugram, India
6d
Handle complaints and conduct product investigations for medical devices, performing inspections and root cause analysis.
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Quality Assurance Technical Specialist (Technical Leader- Tuas Avenue 2)
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Bd Singapore
Tuas, S00, SG
6d
Lead technical quality initiatives, drive investigations for non-conformances and customer complaints, and develop quality documentation for MedTech products.
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Director, IT Solution Owner, QARA
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Olympus Corporation
Center Valley, PA, US
$145k–$145k
6d
Global strategy, governance, and end-to-end ownership of digital solutions for Quality Assurance and Regulatory Affairs (eQMS, RIM, post-market surveillance) to ensure regulatory compliance, audit readiness, and patient safety.
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Training Manager
Medline
Northfield, Illinois, US
$85k–$85k
6d
Plan, direct, and coordinate training and development activities for QA/QC/RA staff across Medline plants, including onboarding and advanced development.
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Dir Manufacturing Quality
Medline
Arlington Heights, Illinois, US
$154k–$154k
6d
Lead the Quality team to ensure product and process compliance for Medline medical devices and drug combination products, developing strategies and executing long-term goals.
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Dir, QA (Product Quality)
Medline
Northfield, Illinois, US
$154k–$154k
6d
Lead Quality teams to ensure product quality and compliance for Medline branded medical device and drug combination products.
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Quality Engineer III
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Pride Mobility
Duryea, PA, US
$75k–$75k
6d
Provides technical leadership and strategic direction for quality engineering initiatives ensuring product, processes, and suppliers meet regulatory and customer requirements.
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Sr Engineer Quality
Medline
Chicago, Illinois, US
$101k–$101k
6d
Setting quality standards, developing testing methods, and ensuring compliance with regulations for medical device production processes.
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VP Manufacturing Quality (Devices)
Medline
Northfield, Illinois, US
$234k–$234k
6d
Lead Quality Assurance functions for assigned divisions, ensuring compliance with US FDA, EU MDR, and cGMP requirements while overseeing new product development and supplier qualification.
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Quality Engineer
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Medbio
Grand Rapids, MI, US
$80k–$80k
6d
Support customers with complaints and corrective actions while assisting engineering in production, metrology, and auditing activities to maintain ISO/cGMP compliance.
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Quality Assurance and Quality Control Officer
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Employment Hero
Smithfield, NSW, AU
6d
Ensuring effective implementation and adherence to the site's Quality Management System in a contract sterilisation and decontamination environment.
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VP Manufacturing Quality (Kitting)
Medline
Northfield, Illinois, US
$234k–$234k
6d
Lead Quality Assurance functions for assigned divisions, ensuring compliance with US FDA, EU MDR, and cGMP requirements while overseeing new product development and supplier qualification.
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Engineer Quality
Medline
Chicago, Illinois, US
$79k–$79k
6d
Independently set quality standards, develop testing methods, and manage vendor quality for medical device production processes.
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VP Product Quality
Medline
Northfield, Illinois, US
$234k–$234k
6d
Lead Quality Assurance functions and set strategic direction for assigned divisions, ensuring compliance with US FDA, EU MDR, and cGMP requirements.
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