Medical Device jobs

Our client is a manufacturer of metal machined components serving the medical device industry. Their product is used in critical devices and quality is at the forefront of everythingn they do. With their developed team, they are looking for a senior level quality engineer to lead both internal and external projects.

The Quality Engineer (Medical Device) will ensure that all products and processes meet established medical device quality standards by overseeing supplier quality, conducting validations, and implementing corrective actions for injection molded and purchased components. They will also develop and maintain quality control systems to support the full product lifecycle in a clean room manufacturing environment.

This role focuses on developing and optimizing catheter manufacturing and assembly processes, transferring designs from R&D to full-scale manufacturing, and improving existing products for scalability and performance. The engineer will design and validate processes, create components and fixtures, conduct experiments, and collaborate with cross-functional teams to bring complex catheter systems from concept to commercialization.

Our client is a well-established medical device manufacturer headquartered in the northern suburbs of Chicago. With more than 15 facilities nationwide and a workforce of over 5,000 employees, they continue to grow through the launch of new product lines. To support this expansion, they are looking for a Senior Quality Engineer to join the Quality team and lead quality oversight for three production lines.

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 Senior Quality Engineer to join their Quality team and take responsibility for overseeing three production lines.

Our client is a leading medical device manufacturer based in the northern suburbs of Chicago. With more than 15 facilities across the U.S. and a team of 5,000 employees, they continue to expand their product portfolio. They are currently seeking a Senior Quality Engineer to join their Quality team and take ownership of three production lines.

Our client is a medical device manufacturer located in the Northern Suburbs of Chicago. With over 15 locations throughout the US and 5000 employees, they have continued to grow out new product lines. They seek a Senior Quality Engineer to join their Quality team and oversee 3 production lines.

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Reporting into the Site Lead, the Senior Manufacturing Manager will oversee and optimize manufacturing operations, ensuring efficient production processes and quality standards are consistently met. The Senior Manufacturing Manager will be responsible for optimizing resources to achieve safety, quality, schedule, and cost goals, while maintaining compliance with internal policies and external regulations - including environmental, OSHA, and FDA standards.

This position oversees manufacturing, packaging, and labeling of finished goods. The role ensures products meet specifications, quality standards, and production schedules while managing resources to achieve safety, cost, and delivery objectives.

The Design Quality Engineer ensures that all medical device design and development activities meet safety, performance, and regulatory standards. This role partners with cross-functional teams to support new product development and sustaining engineering projects, driving quality, compliance, and risk management throughout the design lifecycle

The Quality Manager leads the company's Quality Systems in compliance with ISO 13485 and global medical device regulations, ensuring robust oversight of product release, CAPA, audits, and technical investigations. This role is critical in maintaining regulatory readiness and driving continuous improvement across the organization's quality operations.

The Supplier Quality Engineer will qualify and audit suppliers, validate new products, and ensure compliance with ISO 13485, AS9100, and ISO 9001 standards while supporting NPI projects and resolving supplier-related issues. They will also monitor supplier performance, drive corrective actions, and collaborate across teams to maintain quality and regulatory compliance throughout the global supply base.

As a Senior Program Manager in the life science industry, you will oversee complex projects within the engineering and manufacturing department, ensuring their successful execution from initiation to completion. This role requires strong leadership and organizational skills to manage cross-functional teams.

The Design Quality Engineer plays a critical role in ensuring product designs meet regulatory and internal standards throughout development. This position leads risk management and supports design verification, while also contributing to CAPA investigations and continuous improvement efforts.

The Project Engineer/Manager leads and manages medical device product development and manufacturing transfer projects from concept through production. The position combines hands-on engineering design, regulatory compliance, and project management to deliver high-quality products in a fast-paced, startup-like environment.

We are seeking a Design Quality Engineer to join a medical device/regulated‑industry team. In this role, you will help ensure that products meet safety, regulatory, and business requirements throughout the design lifecycle. You will work closely with cross‑functional teams on both new product development and sustaining projects of complex electromechanical systems (with software and disposables).

Lead full-cycle new product development (NPD) and manufacturing transfer projects from concept through production, ensuring compliance with FDA QSR and ISO 13485 standards. Perform hands-on design and prototyping using SolidWorks, 3D printing, and precision tooling while coordinating cross-functional teams to deliver innovative medical device solutions.

Under limited supervision, the Mold Maker builds, repairs, and maintains in-house molds and tooling using both internal equipment and external suppliers as needed. The role demands strict adherence to tight specifications and tolerances to ensure high-quality standards.

Our client is a premier sheet metal fabrication and injection molding company serving the industrial and medical device markets. They are looking for a Quality Engineer to join their growing quality team. The ideal candidate is a technically skilled engineer who excels in a dynamic environment and demonstrates a proactive, team-oriented approach.

This opportunity gives you the ability to work on the development and optimization of manufacturing processes for high-precision medical components. You will have the chance to collaborate with cross-functional teams to improve quality, streamline production and ensure compliance with the medical industry standards.

This Process Engineer will develop and refine catheter manufacturing and assembly processes, supporting the full product lifecycle from R&D transfer through large-scale production. The role requires strong analytical skills, technical expertise in catheter manufacturing techniques, and the ability to solve complex engineering challenges while collaborating with cross-functional teams.

As a Senior Process Engineer, you will play a key role in developing and optimizing catheter manufacturing processes within the life science industry. This position is based in Marlborough and offers an exciting opportunity to contribute to innovative advancements in engineering and manufacturing.

Our client is a leading sheet metal fabricator and injection molder serving the industrial and medical device sectors. They are seeking a Quality Engineer to join their expanding quality team. The ideal candidate will be a technically strong engineer who thrives in a fast-paced environment and brings a proactive, collaborative personality to the role.