Device Quality Jobs

Philips is hiring a Senior Supplier Quality Engineer to lead supplier quality assurance, process validation, and continuous improvement for medical device components.

Lead cross-functional clinical readiness and device management for early-stage device and combination product trials at AbbVie's North Chicago R&D site.

Nemera seeks a Quality Validation Engineer to lead validation projects, supplier quality activities and investigations to maintain regulatory and ISO compliance at its Buffalo Grove medical device manufacturing site.

AbbVie’s DCPD team is hiring a Senior Project Manager to lead clinical trial readiness and cross-functional coordination for complex device and drug-delivery systems in early-stage development.

Senior Director of Operations to lead and scale manufacturing, supply chain and quality for CVRx’s Barostim® program at our Brooklyn Park, MN headquarters.

Experienced R&D Engineer II to design and execute verification/validation testing and develop new test methods for drug/device combination products at AbbVie's Irvine site.

Dandy is hiring a Senior Quality Engineer to lead ISO-driven quality systems, CAPA, and validation efforts for its manufacturing operations supporting dental prosthetics and medical-device-grade processes.

Lead device and combination-product clinical readiness at AbbVie by coordinating cross-functional teams to enable successful early-stage clinical trials.

Senior Supplier Quality Engineer role at Penumbra to lead supplier qualification, drive corrective actions, and improve supplier performance for medical device products.

Experienced CMC leader sought to drive global product development strategy, lead cross-functional teams, and ensure regulatory-ready CMC deliverables for AbbVie's development portfolio.

Lead the design and operation of OrganOx's QMS and document services, driving eQMS excellence, compliance, and a high-performing global team.

Intuitive seeks a Senior Supplier Engineer to lead supplier qualification and development activities that secure high-quality, scalable supply for its minimally invasive surgical platforms.

Penumbra is hiring a Quality Monitoring & Improvement Specialist I to support CAPA, NCR, and DA processes, coordinate board reviews, compile quality trending data, and assist with audits at the Alameda site.

Echo Neurotechnologies is hiring a Sr. Quality Engineer to lead QMS implementation and design quality assurance for cutting-edge BCI medical devices.

Lead the engineering strategy and execution for electromechanical combination products at AbbVie, overseeing global projects, technical compliance, and team development.

Medtronic is hiring a Senior Hardware Quality Engineer to lead hardware quality assurance, design verification, and regulatory compliance efforts for medical devices at the North Haven site.

Owlet seeks a detail-oriented Quality Specialist I/II to manage complaint intake and investigations, evaluate regulatory reportability, and support QMS activities to ensure product safety and compliance.

Lead the Quality Control team at Gerresheimer's Peachtree City facility, overseeing shift operations, audit readiness, and continuous improvement in a regulated manufacturing environment.

Owlet is hiring a detail-oriented Quality Assurance Engineer to lead manual and exploratory testing of firmware and iOS/Android apps for its FDA-classified baby care devices while supporting regulatory documentation and future automation efforts.

Experienced Manufacturing Technician needed to support process development, equipment setup, validation, and continuous improvement in an onsite production environment.

Sentec is hiring a Supplier Quality Engineer to oversee supplier qualification, audits, and continuous improvement for electromechanical and injection-molded components in a regulated medical device environment.

Lead cross-functional clinical readiness efforts for complex devices and combination products within AbbVie's DCPD organization to enable early-stage clinical trials.

QRC Group is hiring a bilingual Quality Systems Documentation Specialist to manage and maintain regulatory documentation and support validation activities at its Vega Baja, PR location.

Oura is looking for a Medical Device Quality Assurance Engineer to drive compliance, risk management, and verification for SaMD across development and lifecycle activities.

Penumbra is looking for an Ops Support Specialist I to provide day-to-day MES support, drive MES implementation tasks, and coach manufacturing users to ensure compliant, efficient production operations.

Experienced quality engineer needed to lead root-cause investigations, SPC rollout, and process-quality improvement across the Milford manufacturing site and global distribution center for Waters Corporation.

AbbVie is hiring an Associate Director of Program Management to lead global device and combination-product industrialization programs, coordinating cross-functional teams to deliver manufacturing transfers and launches.

Nextern is hiring a Sr. Project Manager to lead complex medical device product development projects from concept through commercialization while ensuring regulatory and cross-functional alignment.

Lead provisioning, inventory, and shipping operations to ensure secure, accurate, and timely deployment of patient-facing devices for a growing healthcare technology provider.

VahatiCor seeks a Process Development Engineer to lead catheter process development, transfer, and validation in its onsite Santa Clara manufacturing environment.

Medtronic is hiring a Quality Systems Business Analyst in Northridge to support and optimize eQMS processes and quality metrics for the Diabetes business, ensuring regulatory compliance and continuous improvement.

Flex is hiring a Validation Associate Engineer in Austin to drive validation activities, maintain quality programs, and support regulatory-compliant product development in a medical device manufacturing environment.