Medical Device jobs

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 is a senior‑level Quality Engineering position with a medical device manufacturer located near the Illinois-Wisconsin border. The role oversees all QA/QC functions within a metal fabrication environment.

My client is an electro-mechanical manufacturer for the medical device industry and they are looking for a Quality Assurance Manager to manage the FDA and ISO Quality Management System and ensure products are designed, developed, manufactured, tested, and delivered to ensure customer and regulatory requirements are met.

My client is an electro-mechanical manufacturer for the medical device industry and they are looking for a Quality Assurance Manager to manage the FDA and ISO Quality Management System and ensure products are designed, developed, manufactured, tested, and delivered to ensure customer and regulatory requirements are met.

The Senior Quality Manager will lead the full Quality function-including QA, QC, and Supplier Quality-while developing and executing the site's overall quality strategy to ensure regulatory compliance and consistently high product standards. This position blends strategic leadership with hands‑on oversight, driving a strong quality culture and aligning operations with customer, regulatory, and corporate expectations.

Our client is a prominent medical device manufacturer headquartered in Chicago's northern suburbs, with more than 15 facilities nationwide and a workforce exceeding 5,000 employees. As they continue to grow and introduce new product lines, they are looking for a Quality Manager to join their Quality organization and lead the department's operations.

A new product line is entering development, and my client needs a Quality Engineer to guide its design activities and ensure compliance throughout the process. This position will also take the lead in creating and organizing documentation for the company's quality systems and related programs. The employer is a specialized manufacturer that builds electro-mechanical solutions exclusively for the medical device industry

This role is an Operations Manager position within a metal fabrication company that serves leading OEMs in the medical device industry.

This is a high-level Quality Engineering role with a medical device manufacturer located near the Illinois-Wisconsin border. The position is responsible for overseeing all QA/QC activities within a metal fabrication environment.

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.

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.

The Manufacturing Engineer focuses on developing and optimizing CNC machining processes for high-precision orthopedic implants and instruments.

The position offers hands-on involvement from programming and fixturing through first-article production and continuous improvement.

The Manufacturing Engineer is responsible for developing and optimizing manufacturing methods, tooling, and documented processes to improve efficiency and product quality. This role involves analyzing production challenges, supporting CAD/CAM activities, collaborating with supervisors, and ensuring adherence to technical specifications, safety standards, and continuous improvement initiatives.

The Senior Quality Manager drives quality strategy, ensures regulatory and customer compliance, and leads multiple quality functions. This position requires strong leadership, the ability to influence senior stakeholders, and deep expertise in managing quality systems within medical, life‑science, or similarly regulated industries.

The Manufacturing Engineer focuses on supporting and improving manufacturing processes for advanced optical components. It combines hands-on engineering, process optimization, and cross-functional collaboration to ensure quality and efficiency in production.

The Project Engineer will be responsible for leading design and development project for production. You will be a key player in the full life cycle development of medical device products in a high volume environment.

As a Project Engineer, you'll oversee product development and manufacturing transfers for regulated medical devices.

The position requires strong project management skills and hands-on engineering expertise.

My client is seeking a highly motivated Project Engineer to lead and execute key projects within the life sciences / medical device manufacturing industry. This role requires expertise in engineering and manufacturing processes, ensuring efficient and high-quality outcomes.

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.

In this role, you'll play a key part in new product introduction (NPI) and continuous improvement efforts across Class II and III devices-from CNC‑machined parts to catheter sub‑assemblies and full finished devices. If you love blending hands‑on problem solving with strategic technical leadership, you'll feel right at home here.

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.

You will drive advanced manufacturing process development, CNC programming, and production readiness for medical device components and assemblies. This role supports both new product introduction (NPI) and ongoing manufacturing optimization for Class II and III devices-including CNC‑machined components, catheter subassemblies, and finished device manufacturing.

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.

You will apply your manufacturing and mechanical engineering expertise to support the build, launch, and scaling of sterile medical device products. This includes working closely with cross‑functional engineering, quality, and operations teams to implement robust manufacturing processes, support new product introduction, and ensure consistent output on the production floor.

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.

You will lead the site's manufacturing engineering and automation agenda for a high‑volume, regulated production facility. Partnering closely with operations, you'll optimize complex extrusion, injection molding, and automated assembly lines to ensure safe, reliable supply of life‑sustaining products.