Medical Device jobs

This is a senior-level Quality Engineering role with a medical device manufacturer located near the Illinois/Wisconsin border. The position is responsible for overseeing all quality assurance and quality control activities within a metal fabrication manufacturing environment.

An electro-mechanical manufacturer in the medical device sector is seeking a Quality Engineer to support design control and product development for a new product line, while also contributing to the documentation and enhancement of quality systems and programs.

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.

My client is looking for an experienced Operations Manager to oversee manufacturing operations in a regulated environment. This role ensures compliance with industry standards while achieving safety, quality, delivery, and cost targets. The ideal candidate will lead strategic initiatives, promote a culture of continuous improvement, and guide teams to perform at their highest level in alignment with organizational objectives.

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.

Our client, a prominent medical device manufacturer headquartered in Chicago's northern suburbs, manages over 15 facilities nationwide and employs more than 5,000 professionals. As they continue to grow with the launch of new product lines, they are looking for a Quality Manager to join their Quality team and lead the department's operations.

The Product Development Engineer will drive the design and development of advanced catheter products, ensuring performance, manufacturability, and regulatory compliance. This role focuses on delivering innovative solutions that support rapid growth and improve patient outcomes.

An electro-mechanical manufacturer serving the medical device industry is seeking a Quality Engineer to contribute to design control and product development for a new product line, as well as to aid in the documentation of quality systems and programs.

This is a quality engineering opportunity with an industry leading manufacturer of medical devices, specifically for transport and storage of critical items for surgical procedures.

Reporting to the CTO, the Director will lead both strategic technical leadership and hands-on expertise in time-series analysis of hemodynamic signals. This individual will manage a team of engineers to develop algorithms for the company's technology, with planned FDA clearance. This role can be fully remote (with travel), onsite, or hybrid.

My client is an electro-mechanical manufacturer for the medical device industry and they are looking for a Quality Engineer to support design control and product development on a new product line as well as to help document quality systems and programs.

My client is an electromechanical manufacturer serving the medical device industry, and they are seeking a Quality Engineer to support design controls and product development for a new product line, as well as assist in documenting quality systems and programs.

My client is an electro-mechanical manufacturer serving the medical device industry, seeking a Quality Engineer to support design controls and product development for a new product line, as well as assist in documenting quality systems and programs.

My client is an electro-mechanical manufacturer for the medical device industry and they are looking for a Quality Engineer to support design control and product development on a new product line as well as to help document quality systems and programs.

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.

This is a Sr. Quality Engineer to help support major OEM customers as it relates to their component manufacturing operations with top-notch quality control and assurance - through customer complaint resolution, CAPAs, and root cause analysis.

This is a Sr. Quality Engineer to help support major OEM customers as it relates to their component manufacturing operations with top-notch quality control and assurance - through customer complaint resolution, CAPAs, and root cause analysis.

Our client, a leading medical device manufacturer located in Chicago's northern suburbs, operates more than 15 facilities nationwide and employs over 5,000 people. As the company continues to grow and introduce new product lines, they are seeking a Quality Manager to lead and oversee all activities within the Quality department.

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 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.

Our client, a prominent medical device manufacturer headquartered in Chicago's northern suburbs, manages over 15 facilities nationwide and employs a workforce of more than 5,000. As they continue to grow with the launch of new product lines, they are looking to add a Senior Quality Engineer to their Quality team. This role will be responsible for overseeing three production lines and ensuring the highest standards of quality are maintained.

Are you a Quality Engineering Professional who has strong ISO experience in the Medical Device Manufacturing industry? Do you have a Lead Auditor Certification in ISO 9001, AS9100, ISO 13485, ISO 14001, IATF 16949 etc.? Do you have a degree in Engineering or a related field? If so, please read on and apply to the Quality Systems Engineer (QMS)- Medical Device Manufacturing based near Fall River, MA.

Are you a CMM Programmer and/or a Quality Engineer with CMM and Metrology experience? Do you have 2+ years of experience in the Manufacturing industry (ideally Medical Device or Plastics Manufacturing)? Do you have OPG and supplier quality experience? If so, please read on and apply to the CMM Programmer / Quality Engineer - Medical Device Manufacturing job based in Rochester, NY.