Medical Device jobs

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.

Our client, a leading medical device manufacturer based in the northern suburbs of Chicago, operates more than 15 facilities across the U.S. and employs over 5,000 people. Continuing to expand with new product lines, they are seeking a Quality Manager to join their Quality team and take responsibility for overseeing the department.

The Production Manager will provide day‑to‑day leadership and operational oversight at my client's facility near Wonder Lake, IL. In this role, you will take ownership of managing production activities, driving continuous improvement across manufacturing processes, strengthening team culture, and developing future leaders within the organization.

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.

This Quality Engineer will serve as the U.S.-based lead for quality, compliance, and regulatory coordination for imported medical device products. The role ensures robust oversight of international manufacturing partners and maintains full compliance with FDA and ISO quality system requirements.

My client is seeking a Manufacturing Technician to be involved in hands‑on work building and inspecting components for minimally invasive implantable pulse generators and external programming systems.The ideal candidate is detail‑oriented, quality‑driven, and comfortable working in a regulated, high‑precision medical device production 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.

This role is ideal for an experienced engineer who thrives in a fast‑growing, innovation‑driven medical device environment. You will play a critical role in the development, optimization, and lifecycle management of implantable medical devices designed to improve outcomes for patients with chronic heart failure.

The Manufacturing Lead is responsible for supporting hands‑on medical device production, ensuring high-volume sterile disposables and finished assemblies meet quality, performance, and regulatory expectations. This role contributes technical expertise to product launch, process development, and day‑to‑day manufacturing operations for a novel interventional therapy technology.

The Senior Quality & Regulatory Engineer will serve as the primary U.S. quality lead for Class II spine medical devices, ensuring regulatory compliance and seamless oversight of international manufacturing partners. The role offers autonomy, strategic influence, and direct interaction with FDA, suppliers, and global engineering teams.

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.

We are seeking a highly skilled engineer with a strong background in medical device research and development-particularly in implantable biologic materials. This role is ideal for someone who thrives at the intersection of engineering, biology, materials science, and chemistry. You will contribute to product development, technology transfer, and innovative research supporting a growing biologics portfolio.

The Senior Manufacturing Engineer will be an essential piece in the development of over 90 different products. You will have the opportunity to be hands on development through the manufacturing phase.

The Manufacturing Engineering Manager will lead the mold tooling engineering for complex medical devices and molded components, supporting both new product development and continuous improvement.

You will lead a tooling team, drive excellence, and guide internal and external tool builds from concept through qualification.

This role supports the development and manufacturing of biologic medical devices, focusing on implantable biologic materials. Responsibilities include new product development, process engineering, analytical testing, and validating tissue‑processing steps. The position is highly technical and hands‑on, supporting both existing product lines and new biologic research initiatives.

This Senior Quality Engineer role drives quality system compliance and process development for advanced medical manufacturing projects. You'll lead critical quality engineering initiatives, manage dynamic project loads, and influence best‑in‑class processes from concept through scale‑up.

The Manufacturing Technician supports the development and execution of manufacturing processes for implantable electronic medical devices while overseeing daily metallographic laboratory operations. In this role, you'll work hands‑on with specialized equipment, support engineering teams, and ensure accurate process execution in a high‑quality, safety‑driven environment in Mount Laurel, NJ.

This Senior Manufacturing Engineer role leads CNC programming, advanced process development, and production readiness activities for highly engineered medical device components and assemblies.

The position supports both new product introduction and continuous improvement, with significant ownership over machining strategy, validations, documentation, and cross‑functional technical leadership.

The Senior Quality Engineer role leads critical quality engineering efforts across product development, manufacturing, and post‑market activities for regulated medical technologies. You'll ensure compliance, champion quality systems, and guide cross‑functional teams through validation, risk, and design control work.

The Senior Manufacturing Engineer leads CNC process development, programming, and production optimization for precision medical device components in a fast‑paced, highly regulated environment. This role supports new product introduction and continuous improvement by developing scalable processes, troubleshooting machining challenges, and driving advanced manufacturing excellence.

The Senior Manufacturing Engineer will play a critical role in optimizing manufacturing processes and ensuring high-quality production standards within the medical device manufacturing industry. This position requires a hands-on approach to problem-solving and a focus on continuous improvement in the engineering and manufacturing department.

This Senior Manufacturing Engineer role supports advanced manufacturing for Class II and III medical devices, including CNC‑machined components, catheter subassemblies, and complete device builds.

This Senior Manufacturing Engineer will own advanced CNC machining process development, new product introduction (NPI), and production readiness for precision medical device components and assemblies. The role blends hands-on manufacturing engineering, CNC programming, validation, cross-functional leadership, and continuous improvement to support both legacy and new product lines.

This is a high‑impact, hands‑on manufacturing engineering position supporting the scale‑up and ongoing production of next‑generation medical device assemblies. The Lead Manufacturing Engineer will develop, refine, and validate manufacturing processes; build fixtures and tooling; improve assembly workflows; and ensure production readiness by partnering closely with quality, operations, and engineering teams.

The Senior Manufacturing Engineer supports the manufacturing and scale‑up of complex medical device components and assemblies. The engineer will collaborate closely with cross‑functional teams to refine processes, improve manufacturability, and ensure consistent, high‑quality output. It's a hands‑on position focused on assembly engineering, process documentation, quality compliance, and floor support within a regulated environment.

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.