Medical Devices jobs

The Senior Manufacturing Engineer will be responsible to lead all manufacturing efforts onsite. They will be the first Manufacturing Engineer hire in the entire organization.

Are you passionate about making a positive impact on people's lives through cutting-edge medical devices? In this Senior Manufacturing Engineer role you will be responsible for leading manufacturing process development, optimization, and validation activities for medical device products.

As a Mechanical Designer (Levels I-III), you will support the design and development of innovative medical devices. You'll create 2D and 3D models, assist with prototype development, and contribute to new product introduction. Ideal for individuals who are detail-oriented, creative, and passionate about engineering within a regulated industry.

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!

My client is seeking a highly skilled and motivated Field Service Engineer to provide technical support, installation, repair and maintenance of their analytical instruments at customer sites. The role will cover their newest and most technical product line with customers predominately in the Biotech Industry.

This position is for an IT Business Analyst with experience working in the medical device industry (or a similar highly regulated industry) and ERP experience to join a global medical device manufacturing organization. This is a remote role but you must be based in the US and must be fully authorized to work in the US to be considered.

My client is looking for an NPI Engineering Manager to join their team out of the Providence, RI area. They are looking for someone with strong leadership and managerial skills, the ability to foster teamwork, delegate effectively, and build collaborative relationships.

The Senior Supplier Quality Engineer (Medical Devices) will ensure that suppliers provide high-quality materials and services that meet product quality and regulatory requirements. They will assess supplier capabilities, oversee technical activities, and drive compliance to support business needs at our Hudson, MA facility.

In this position, the Engineering Manager will have the opportunity to work hands-on with a well known medical device manufacturer. This organization emphasizes company culture and is committed to the success of their employees and their customers.

Our client, a prominent sheet metal fabricator and injection molder, also provides welding, powder coating, blanking, and various other manufacturing services for the industrial and medical device sectors.

My client is seeking a new addition to lead their Field Service Engineering and Technical Services Team's Globally. This individual will develop and oversee a comprehensive service strategy to strategically align with my client's business goals and innovations. They will have ownership over customer bases in North America, EMEA, and other regions. This will be a terrific opportunity to make an impact through strategic thinking and coaching/development.

As a Field Clinical Account Specialist you will be providing educational, clinical, and procedural direction to help achieve patient care, customer support, and service objectives. You will interface with and help our customers by being the resident expert on our Hepatic Arterial Infusion (HAI) pump and accessories

The Project Engineer plays a critical role in leading, managing, and executing medical device manufacturing and product development projects.

Opportunity to join a rapidly growing organization in a pivotal role. Utilize CNC knowledge to implement best practices for machining operations.

Be a key leader in an individual contributor role who manages multi-site programs, involving vertically integrated technologies, processes, and businesses. The Program Manager will work and drive production implementation of new products and technologies. The Program Manager will lead facility expansion and transfer projects across the broader organization.

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 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.

As a Quality Manager it involves hands-on laboratory work, primarily focusing on cell culture and flow cytometry, within a team dedicated to developing and validating new assays. The position requires meticulous documentation and adherence to established protocols, contributing directly to the advancement of cell analysis technologies.

The Quality Engineer will manage and improve the company's ISO 13485 compliant quality systems, ensuring process and product excellence through data-driven analysis and validation. This role involves cross-functional collaboration, regulatory compliance, and qualifying the company for new business opportunities.

The Quality Engineer is responsible for developing and implementing quality policies and procedures to ensure compliance with ISO 13485, while leading or supporting investigations into manufacturing issues, non-conforming products, and customer complaints through CAPA initiatives. They also develop validation protocols, oversee manufacturing process and product qualifications, and analyze data, customer feedback, and quality costs to drive continuous improvement.

As a Quality Engineer you will establish and maintain quality systems, guarantee regulatory adherence, and represent quality within project teams. The role encompasses managing manufacturing quality, leading investigations, and collaborating cross-functionally to uphold stringent product safety and quality benchmarks.