Medical Devices jobs

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.

As the Global Project Manager, you will be responsible for leading and delivering complex, large‑scale projects across global supply and operations, ensuring outcomes are achieved on time, within budget and to the highest quality standards. This is a highly visible role offering exposure to senior stakeholders and the opportunity to drive meaningful operational change.

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.

As the Program Manager, you will leads cross‑functional teams to deliver innovative, software‑enabled electromechanical medical device products through the full development lifecycle. It offers the opportunity to drive complex programs, influence strategic decisions, and help bring life changing technologies to market

This position oversees early‑stage manufacturing operations within a medical‑technology environment, focusing on prototype builds, validation efforts, and the initial phases of production. The role bridges engineering and operations, ensuring new products are assembled reliably through well‑designed processes, solid documentation practices, and disciplined execution before scaling into broader manufacturing.

The Senior Manager of Manufacturing will lead internal manufacturing operations, ensuring new products can be built consistently, safely, and with strong process discipline prior to scale‑up. Sitting at the intersection of engineering and operations, this leader will oversee manufacturing builds, partner with process engineering to develop stable processes, and ensure all documentation and work instructions are in place.

The Senior Advanced Manufacturing Engineer will work on a team that supports the development of new medical devices and improvements on exciting products. In this role, you will work on a variety of engineering tasks including working on product designs, managing complex projects, developing validation protocols and test methods, and working on continuous improvement initiatives.

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.

This role supports hands‑on manufacturing and laboratory operations for complex electronic medical devices. You'll work closely with engineering teams to execute, refine, and document production processes in a highly regulated environment.

This role leads the development and validation of manufacturing processes for complex implantable electronic devices. It also provides technical leadership across cross‑functional teams to optimize quality, efficiency, and product reliability.

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.

As the Senior Mechanical Engineer, Product Development, you will lead the design and development of innovative electromechanical medical products used in high impact clinical applications. You will own product development activities end‑to‑end, collaborating cross‑functionally to deliver robust, manufacturable solutions.

The Senior Manager will oversee day-to-day pilot manufacturing, partner closely with engineering and quality functions, and establish the operational rigor necessary to drive successful product development and manufacturing readiness. The ideal candidate is a strong manufacturing leader who brings technical depth, sound judgment, and the ability to build structure and predictability within a fast-paced medical device environment.

The Senior Manufacturing Engineer will lead advanced process development, CNC programming, and production readiness for medical device components and assemblies. This role supports both new product introduction (NPI) and continuous improvement initiatives for Class II and III medical devices-including CNC‑machined parts, catheter sub‑assemblies, and finished devices.

We are seeking a Senior Manager of Manufacturing to lead and elevate our pilot‑scale manufacturing operations, driving development, validation, and early commercial production for innovative medical technologies.

This role leads all regulatory affairs and quality assurance functions, ensuring global compliance and driving continuous improvement across the organization. You'll oversee submissions, audits, QMS strategy, and partner closely with executive leadership on regulatory direction.

This role leads R&D efforts for implantable biologic materials, supporting product development, test method creation, tech transfers, and early‑stage research. You'll design manufacturing steps, run analytical testing, and contribute to expanding the biologics portfolio.

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.