Medical Device jobs

My client is an electro-mechanical manufacturer for the medical device industry and they are looking for a Quality Engineer who will be responsible for hands-on investigation and failure detection of electro-mechanical medical devices.

My client is an electro-mechanical manufacturer for the medical device industry and they are looking for a Quality Engineer who will be responsible for hands-on investigation and failure detection of electro-mechanical medical devices.

My client is an electro-mechanical manufacturer for the medical device industry and they are looking for a Quality Engineer who will be responsible for hands-on investigation and failure detection of electro-mechanical medical devices.

My client is a manufacturer specializing in electro-mechanical systems for the medical device sector, and they are seeking a Quality Engineer to conduct hands-on troubleshooting, root cause analysis, and failure investigation of electro-mechanical medical devices.

My client is an electro-mechanical manufacturer for the medical device industry and they are looking for a Quality Engineer who will be responsible for hands-on investigation and failure detection of electro-mechanical medical devices.

This role focuses on designing and developing electronic systems for advanced medical devices used in critical care environments. The position involves hands-on circuit design, testing, and cross-functional collaboration to bring high-reliability products to market.

This Manufacturing Engineer leads manufacturing process development and costing strategies within a precision medical device environment. The role combines hands-on engineering, new product introduction, and commercial quoting to drive operational and financial performance.

This Quality Engineer will play a critical role in maintaining regulatory compliance while supporting production, investigations, and facility transfer activities. The position blends hands‑on manufacturing support with system‑level quality engineering in a fast‑paced medical device environment.

This Electrical Engineer focuses on designing and supporting electrical systems for next‑generation medical devices used in critical care environments. The position blends R&D work on new products with sustaining engineering for recently released technologies

This role leads all quality activities across manufacturing, supplier management and compliance in a regulated production environment. You'll own the Quality Management System while partnering closely with engineering and operations to drive continuous improvement.

Seeking an experienced Engineering Project Manager to oversee complex NPI programs from concept through production transfer within a regulated medical manufacturing environment. This role will drive project execution, customer communication, manufacturing coordination, and commercialization efforts while ensuring timelines, deliverables, and operational goals are achieved.

As a Quality Engineer, you'll partner cross‑functionally with engineering, manufacturing, and operations to ensure product and process excellence in a regulated environment. You'll drive continuous improvement, lead validation and CAPA activities, and play a hands‑on role in maintaining world‑class quality standards.

This role is responsible for leading and managing the Quality Management System, ensuring compliance with ISO 9001 and ISO 13485 while driving continuous improvement across manufacturing operations. You will oversee audits, CAPA, supplier quality and validation activities while directly leading and developing the Quality team.

This role is responsible for leading the design, development, and customization of spinal implant instrument systems from early concept through commercialization. The position integrates closely with implant design teams and works directly with U.S. spine surgeons to refine surgical workflows, ergonomics, and system performance. The engineer will play a critical role in shaping surgeon-facing instrumentation for fusion procedures.

The Program Manager with lead the end‑to‑end development and commercialization of complex medical devices, including capital equipment, disposables, and software‑enabled systems. The focus is on program execution, schedule and risk management, design controls, and coordination across R&D, Quality, Regulatory, and Operations in a regulated environment.

The Senior Test Engineer will design, develop, and validate robust test equipment and processes that ensure the quality and reliability of my client's medical devices from prototype through production. This hands‑on role blends hardware, software, and manufacturing collaboration to drive efficient, compliant testing in a regulated medical device environment.

This Program Manager will lead cross‑functional teams through the development and commercialization of complex medical device systems, including capital equipment, disposables, and software-enabled products. This position ensures programs meet technical, regulatory, schedule, and budget objectives from concept through launch.

The Senior Quality Engineer is responsible for leading and maintaining processes across the product lifecycle in compliance with applicable regulatory standards and internal quality requirements. This role ensures that product risks are systematically identified, evaluated, mitigated, and monitored, supporting the development and commercialization of their product line.

This role partners closely with engineering, manufacturing, and operations to ensure product and process quality across a regulated medical device environment. You'll lead validation, problem-solving, and continuous improvement initiatives with a strong focus on defect prevention and compliance.

Seeking a highly skilled Manufacturing Engineer to lead process development, manufacturing optimization, and quoting activities within a medical device contract manufacturing environment. This role will support both base business improvements and new product launches while collaborating across engineering, production, commercial, and customer teams to improve quality, delivery, and cost performance.

The NPI Engineering Project Manager will lead end-to-end new product introduction (NPI) programs, ensuring successful execution from initial quote through production launch.This role bridges engineering, operations, and commercial teams, serving as the primary point of contact for both internal stakeholders and customers. The ideal candidate combines strong technical knowledge, project management discipline, and customer-facing experience.

The Senior Manufacturing will lead process development, new product introduction (NPI), and quoting efforts, while driving improvements across quality, delivery, and cost. This is a highly visible position that works cross-functionally with engineering, operations, and commercial teams.

The Process Controls Engineer is a hands-on engineering role focused on improving manufacturing safety, quality, and efficiency through the design, implementation, and support of automated systems and process controls. The position involves troubleshooting, project management, and collaboration across teams using PLC programming, electrical/mechanical systems, and data-driven process improvements in Southampton, PA.

This Quality Manager will lead and maintain a robust Quality Management System, ensuring compliance with ISO standards while driving continuous improvement across manufacturing and supplier quality. Acting as Management Representative, you'll partner closely with leadership and production teams to ensure product quality, regulatory compliance, and operational excellence.

The Senior Mechanical Engineer will work on the design and development of innovative disposable and electromechanical medical devices that support life‑saving technology. This role combines hands‑on engineering, cross‑functional collaboration, and technical leadership to bring products from concept through commercialization.

This role is ideal for a hands on Senior Test Engineer who is an expert in verification and validation and enjoys designing, validating, and optimizing test systems for complex electro-mechanical products. You will play a key role in ensuring robust, compliant manufacturing test processes from prototype through full production.

This role leads a manufacturing engineering team within a regulated environment, overseeing new product introduction, process development, and ongoing production support while ensuring compliance with quality and safety standards. It focuses on driving operational excellence through continuous improvement, cross-functional collaboration, and data-driven decision-making to enhance efficiency, quality, and cost performance.

This position leads a manufacturing engineering team supporting new product introduction, process development, and sustaining operations. The role partners cross‑functionally to improve quality, cost, throughput, and compliance while building a culture of accountability and continuous improvement.

This role leads a manufacturing engineering team to support product launches, process development, and ongoing production in a regulated environment. It focuses on driving efficiency, quality improvements, and continuous improvement initiatives while ensuring compliance and cross-functional alignment.

This is a highly autonomous Quality Engineer role where you'll lead US regulatory and quality oversight for FDA‑cleared implantable medical devices manufactured overseas. You'll act as the primary FDA liaison while building and maintaining a compliant, inspection‑ready quality system across international partners.