Medical Device 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 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.

My client is looking for a Senior Development Engineer to join their growing organization. This role is part of a cross-functional engineering team focused on driving the design, development, verification, and manufacturing transfer of innovative 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.

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.

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.

The Development Engineer will be a key player in the development and design of catheters for some of the largest medical device and health-care organizations across the country.

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

The Program Manager will oversee and coordinate cross-functional projects, ensuring the successful delivery of cutting-edge medical devices through effective collaboration with internal teams and external partners. With a strong background in laser-based systems and a deep understanding of regulatory standards, the Program Manager will drive accountability, manage project finances, and proactively address risks, all while maintaining a focus on high-quality execution and continuous process improvement.

Oversee product quality from development to delivery, working closely with customers, while supporting and maintaining the QMS (ISO 13485) to ensure compliance with industry standards. Lead new product introductions, interpret GD&T drawings, develop measurement methods, program vision systems (OGP Smart Scope), and utilize SPC, DOE, and Gage R&R for continuous process improvement and root cause analysis.

The Quality Engineer, Medical Device Manufacturing, will lead efforts to ensure product quality and compliance by developing and implementing quality processes, investigating non-conformities, and driving continuous improvement initiatives. This role requires a hands-on approach, working closely with manufacturing, engineering, customers, and suppliers to uphold the company's quality standards.

The Senior Manufacturing Engineer will be an essential piece in the development of over 90 different products. You will have the opportunity to be hands on development through the manufacturing phase.

The Senior Manufacturing Engineer will be an essential piece in the development of over 90 different products. You will have the opportunity to be hands on development through the manufacturing phase.

The Sr. Sustaining Manufacturing Engineer will be responsible for current products currently on the market while growing a team of manufacturing and process engineers along the way. The team is seeking to add 10 new talented individuals to their production, supply chain and quality team throughout 2025.

The Quality Manager, medical device manufacturing, will ensure products meet strict quality standards while driving continuous improvement to enhance reliability and performance. This role focuses on optimizing operational efficiency and implementing technical solutions to deliver high-quality products on time at our Bedford, MA facility.

Our client specializes in sheet metal fabrication and injection molding for the industrial and medical device sectors, and they're seeking a Quality Engineer to join their expanding quality team. They're looking for a skilled engineer who thrives in a fast-paced environment and brings an outgoing, collaborative personality.

As the Senior Manufacturing Engineer, you will lead the development and improvement of medical devices, working on new products, product enhancements, and technology transfers. You'll manage complex tasks such as prototyping, testing, data analysis, and project management while ensuring products meet performance specifications. You will collaborate with surgeons, gather feedback, and oversee the procurement of materials. Your role will involve using engineering software, developing test methods, and recommending cost improvements to enhance product quality and efficiency.

Provide technical expertise (SME) for assigned equipment and machine control systems. Participate in and lead equipment troubleshooting and problem solving. Complete independent analysis and develop solutions to problems. Identify and evaluate opportunities for process equipment, machine control, network/server improvements and cost savings. Use creative approaches in solving complex problems.

The Controls Engineer will provide technical expertise for manufacturing equipment and machine control systems. This role involves troubleshooting, programming, and optimizing automation technologies to improve efficiency, quality, and compliance in a regulated environment.

The R&D Engineer will play a crucial role in designing and advancing catheter technology for major healthcare and medical device companies nationwide.

The Field Service Engineer is a critical element in ensuring customer satisfaction with my client's manufactured and distributed products. This position is responsible for performing onsite repairs and installations, preventative maintenance, client training, triaging calls and promoting service contracts. The Field Service and Support Engineer must maintain the highest standards in courtesy and competence with the company's customers.

Join a rapidly growing medical technology company as a Field Service and Operations Technician, providing installation, maintenance, and technical support for precision surgical equipment with 20% travel. This hybrid role offers a competitive salary, bonus potential, excellent benefits, and career growth in a company specializing in advanced energy surgical solutions-apply today!

This position is for a talented Embedded C++ Software Engineer to join an industry leading medical device organization just south of Boston to help lead and shape the future of their software engineering division, whilst working on some revolutionary medical devices.