Medical Devices jobs

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.

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.

My client is seeking an experienced Operations Manager to lead manufacturing operations within a regulated environment. This role is responsible for ensuring compliance with industry standards while meeting safety, quality, delivery, and cost objectives. The ideal candidate will drive strategic initiatives, foster a culture of continuous improvement, and provide leadership to develop high-performing teams aligned with organizational goals.

The quality engineer will help lead all quality-driven activity associated with the design and manufacturing of precision medical devices and components. The ideal candidate will help lead all audits, handle QA/QC activity, and work cross-functionally with engineering teams to ensure product and customer standards are met.

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.

This is a quality manager opportunity with a manufacturer that produces medical devices for some of the big players in the industry. This role will have primary oversight of the quality department, leading QA/QC operations, validations, and owning KPIs.

Are you a Quality Manager in the Medical Device Manufacturing Industry? Are you local to Greenville, NC or want to relocate to the Carolina's? Do you have ISO 13485 and a strong root cause analysis background? Do you want to drive compliance and continuous improvement? If so, please read on and apply to the Quality Manager - Medical Device Manufacturing job based near Greenville, NC.

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 Production Manager will lead manufacturing operations for a growing medical device company. This role is critical to ensuring production goals are met while maintaining strict regulatory compliance and high product quality. The ideal candidate will be a hands-on leader with experience in lean manufacturing and continuous improvement.

We are seeking a motivated Development Engineer to join a medical device organization. The ideal candidate will be responsible for developing and implementing engineering solutions to meet our project requirements, with a particular focus on applications related to medical device implants. This role involves designing and optimizing components that meet stringent regulatory standards and supporting innovation in implantable technologies.

The Development Engineer focuses on the full lifecycle development of surgical instruments supporting spinal implant systems. The role involves design, customization, regulatory compliance, and close collaboration with surgeons and implant design teams to deliver innovative, ergonomic solutions for complex procedures.

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.

This position is responsible for developing and optimizing CNC machining processes for highly precise medical device components in a fast‑paced, regulated manufacturing environment. The engineer will lead programming, process validation, and continuous improvement initiatives to enhance quality, throughput, and overall operational performance.

The position leads design assurance activities for new product development, ensuring full compliance with FDA, ISO, and global medical device regulations. It drives quality engineering efforts across the product lifecycle, including risk management, verification/validation, and process validation, while supporting cross‑functional teams and suppliers.

The Senior Manufacturing Engineer will play a pivotal role in optimizing production processes and ensuring efficient operations within the Engineering & Manufacturing department. This position focuses on driving continuous improvement initiatives, enhancing product quality, and supporting advanced manufacturing techniques such as extrusions for medical device applications.

The Quality Engineer will be responsible for ensuring compliance with medical device standards, driving root cause analysis, corrective actions, and continuous improvement through statistical and risk management practices. The position involves supporting validations, environmental monitoring, and quality system reporting to uphold product reliability and regulatory requirements.

My client is seeking a Quality Engineer to support product quality, compliance, and process excellence at a leading medical device manufacturer. This role is ideal for someone who thrives in a hands‑on, regulated environment and enjoys driving root‑cause problem solving, validations, and continuous improvement.