Medical Devices jobs

The Quality Engineer is responsible for overseeing the continual improvement of medical devices and the design and manufacturing of new devices. This role involves developing QA procedures, assessing regulatory standards, leading design control projects, and ensuring product quality through various analyses and audits.

The Project Engineer will be a key leader in the execution of medical device manufacturing and product development projects, ensuring delivery within scope, on time, and in alignment with company goals. In this role you will be customer facing, communicating with them directly to ensure that projects are moving along smoothly.

The Controls Engineer III will provide technical leadership for the evaluation and implementation of automation and controls improvements to enhance the efficiency, quality, compliance, and safety of manufacturing operations. Evaluate existing process controls and suggest and evaluate controls improvements.

This role will be a part of a cross-functional engineering team driving the design, development, verification, and manufacturing transfer of novel interventional medical devices.

The Quality Engineer (medical device manufacturing) plays a key role in ensuring product and process quality through all phases of development, validation, and production, in compliance with ISO 13485 and FDA regulations. This individual will lead root cause investigations, support design controls, and drive continuous improvement initiatives in a fast-paced, innovation-focused environment.

My client is seeking the Quality Manager will lead a dynamic team in a growing medical technology facility, overseeing all quality systems and ensuring compliance with FDA and ISO-13485 standards. This role combines strategic leadership and hands-on management to drive continuous improvement, support regulatory readiness, and foster a culture of operational excellence at the Buffalo, NY facility.

My client is seeking the Quality Manager will lead a dynamic team in a growing medical technology facility, overseeing all quality systems and ensuring compliance with FDA and ISO-13485 standards. This role combines strategic leadership and hands-on management to drive continuous improvement, support regulatory readiness, and foster a culture of operational excellence at the Buffalo, NY facility.

As the Quality Engineer you will gain hands on experience in medical device development, focusing on manual testing, design controls, sterilization, and transit testing. You will collaborate closely with mechanical engineers and cross functional teams to ensure compliance with FDA regulations and ISO 13485 standards.

The Quality Manager (Medical Devices) will lead a dynamic team in a growing medical technology facility, overseeing all quality systems and ensuring compliance with FDA and ISO-13485 standards. This role combines strategic leadership and hands-on management to drive continuous improvement, support regulatory readiness, and foster a culture of operational excellence at the Buffalo, NY facility.

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.

As a Project Engineer, you will lead and manage key projects in the medical device industry, driving product development and manufacturing transfers from concept through production. You'll collaborate closely with customers and cross-functional teams, utilizing your engineering expertise to design solutions, ensure quality compliance, and optimize manufacturing processes. Your contributions will directly impact project success and company growth.

The Project Engineer is a key driver of innovative medical device projects, leading development and manufacturing efforts from concept to launch-delivering results on time and in compliance with FDA and ISO 13485 standards.

My client, a leader in the medical device space, is seeking a Manufacturing Engineer to come support their manufacturing efforts in a hands-on capacity. In this position, the Manufacturing Engineer will have the opportunity to work with leading medical device technology.

The Quality Manager, medical device manufacturing, will lead the maintenance and continuous improvement of the quality management system to ensure compliance with regulatory standards and internal requirements at our Marlborough facility. They will oversee supplier quality, incoming inspection, and production support to drive consistency in product and process quality across the organization.

My client is seeking a skilled Manufacturing Engineer who will drive the development, optimization, and support of manufacturing processes for life-saving surgical devices. You'll collaborate closely with R&D, Quality, and Production teams to ensure our products meet the highest standards of safety, performance, and regulatory compliance.

The Manufacturing Engineer will be responsible to assist with all manufacturing efforts onsite. They will be the second Manufacturing Engineer hire in the entire organization.

Join a fast-paced, collaborative team where you'll lead high-impact manufacturing projects from concept through launch, driving cross-functional teams to deliver innovative solutions on time and within budget. This is a high-visibility role ideal for a hands-on project leader who thrives in dynamic environments, loves solving complex problems, and is excited to make a real impact across global operations.

As the Development Engineer, you will lead the design and development of innovative catheter-based medical devices. You'll refine product concepts, create detailed CAD designs, and prototype new solutions. Collaborating with cross-functional teams, you will drive in-vivo and in-vitro study protocols, and ensure manufacturing processes meet the highest quality standards. This role offers the chance to make a significant impact in the medical device industry while advancing cutting-edge healthcare solutions.

The Quality Engineer leads root cause investigations and performs employee training on quality procedures, while also assisting with quality management system improvements. Their duties include developing measurement methods, analyzing manufacturing data, conducting audits, and maintaining quality documents.

This Quality Manager role oversees the quality management system, ensuring compliance with global regulatory standards and driving continuous improvement across manufacturing and operations. It's a high-impact position ideal for someone passionate about quality, innovation, and making a real difference in the medical device industry.

The Senior Manufacturing Engineer will wear many hats and support a small manufacturing environment. In this role you will get to work autonomously, supporting the manufacturing of new and existing surgical medical devices.

The Manufacturing Engineer will sit on a small team reporting into the Manufacturing Engineering Manager. In this role you will get to work autonomously, wearing many hats, supporting the manufacturing of surgical medical devices.

My client is seeking a highly experienced Manufacturing Engineer to join their team in a hands-on role within a small company environment. The ideal candidate will have a strong manufacturing engineering background, with extensive experience using small shop machinery and SolidWorks. This is not an R&D position, but some design work will be required. The role will involve the development, improvement, and implementation of manufacturing processes, as well as collaborating closely with production teams to ensure efficient operations.

This Quality Manager role requires ensuring cGMP and ISO 13485 compliance, managing quality systems, handling regulatory processes such as CAPA and recalls, and securing successful audits. The position also encompasses continuous improvement initiatives, data analysis, team leadership, and supplier quality management to assure the dependability and uniformity of medical devices.

The Quality Manager, medical device manufacturing, will lead the maintenance and continuous improvement of the quality management system to ensure compliance with regulatory standards and internal requirements at our Marlborough facility. They will oversee supplier quality, incoming inspection, and production support to drive consistency in product and process quality across the organization.

The Senior Quality Assurance Engineer will lead both quality and design assurance activities. This role involves developing and implementing quality management systems, ensuring compliance with regulatory standards, and collaborating with cross-functional teams to support product development and manufacturing processes.

My client, based in Springfield, MA, is seeking a detail-oriented, self-motivated individual to manage multiple projects at various stages. As a project lead, you'll oversee all controls engineering tasks to ensure successful project completion. My client looks for dedicated individuals passionate about precision, innovation, and continuous improvement

This role is an exciting supplier quality engineering role with an opportunity to lead both internal quality projects and external communication with suppliers and stakeholders. You will work on a skilled team that produces very exciting products for various industries.

The Quality Manager will be responsible for ensuring products meet rigorous quality standards while driving operational efficiency and implementing technical solutions to enhance reliability and performance. They will focus on continuous improvement to guarantee timely delivery of high-quality products that meet customer expectations.

The Quality Engineer develops and implements quality policies to ensure ISO 13485 compliance, leads investigations into manufacturing issues, non-conformances, and customer complaints through CAPA initiatives. They also create validation protocols, oversee process and product qualifications, and analyze data, feedback, and quality costs to drive continuous improvement