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Senior Electromechanical Product Developmen Engineer - Medical Devices : MA-Foxborough
Job in
Foxborough, Norfolk County, Massachusetts, 02085, USA
Listed on 2026-06-04
Listing for:
Sage Product Development, Inc.
Contract
position Listed on 2026-06-04
Job specializations:
-
Engineering
Product Engineer
Job Description & How to Apply Below
Benefits
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Paid time off
Sage Product Development, Inc. provides fast, efficient and creative product development services to medical device companies. We are a focused team of experienced medical device engineers who know what it takes to develop successful products for startups, multinational companies, and everyone in between. We combine a high level of experience with a low overhead company structure. We solve client companies’ technical challenges and meet their product development needs in a timely, efficient and highly personalized manner.
We offer the right candidate the opportunity to work in an entrepreneurial environment, enhance their product development and electromechanical engineering abilities, and build their network within the industry.
- Develop medical devices from concept through market introduction on a contract basis for client companies.
- Meet or exceed customer expectations.
- Manage product development projects. Prepare project plans that specify project phases, tasks, task interdependencies, durations, resource assignments, and costs. Proactively communicate task assignments to responsible individuals and ensure that tasks are completed within the planned time. Track projects to project plans. Proactively report project status to Sage personnel and to the project’s client company.
- Generate project timing and expense estimates and prepare project proposals for client companies.
- Design and develop medical devices (disposable and reusable), catheters, equipment, implants, and/or packaging, from concept through market introduction. Ensure that designs meet performance specifications, regulatory and manufacturing requirements.
- Interact with client companies in a professional manner. Proactively communicate with client companies to ensure an ongoing two‑way exchange of information.
- Generate innovative concepts for new medical device designs to satisfy customer and clinical requirements. Provide input on electromechanical considerations across multiple projects. Lead and participate in concept generation activities, including brainstorming sessions. Refine, rate, rank and/or otherwise assess concepts.
- Design and prototype electromechanical systems. Program prototype microcontrollers. Utilize Solid Works to develop detailed 3‑D CAD models and drawings, including component, subassembly, and top-level drawings.
- Research and select electrical and electromechanical components such as sensors, actuators, controllers, connectors and boards. Investigate and evaluate existing technology for application to projects.
- Design and implement new methodologies, materials, machines, processes or products as required to achieve product development goals.
- Collaborate with consultants and vendors to guide custom circuit board and software design. Produce prototype devices for testing and evaluation. Work with internal and/or external resources to produce prototype device components. Assemble and/or evaluate prototype devices. Build and debug electromechanical assemblies including soldering, wiring, board assembly and mechanical assembly.
- Conduct bench and/or animal feasibility studies.
- Conduct product verification and validation testing to demonstrate product safety and efficacy. Manage software validation activities. Determine what testing is required to satisfy product requirements, to investigate potential failure modes, and to otherwise address the project design inputs. Develop protocols, plan testing, and perform or monitor testing. Utilize statistical methods as required to plan testing and to analyze test results. Write test reports which draw conclusions from the results.
- Conduct risk analyses. Conduct and document Failure Mode and Effects Analyses. Manage ISO 60601, ISO 61010, EMC and/or EMI testing at outside vendors and troubleshoot failures.
- Coordinate activities with outside suppliers and consultants to ensure the delivery of supplies or services needed to meet customer expectations.
- Maintain detailed essential product and process documentation throughout all phases of research and development. Maintain Design History Files (DHFs). Ensure that DHFs are accurate, complete and well organized.
- Prepare documentation release packages, including detail drawings, bills of material, and/or procedures. Approve Document Change Orders (DCOs) and obtain approvals from others as required.
- Ensure that all work satisfies the requirements of client companies’ Quality Systems, with particular emphasis on Design Control.
- Conduct and document Design Reviews.
- Participate in Material Review Board activities. Make decisions regarding product and material discrepancies and initiate appropriate action to prevent subsequent problems or discrepancies.
- Date, sign and have witnessed all documents that may establish inventorship dates.
- Some local travel (i.e. by car). Occasional long‑distance travel (i.e. by plane).
Position Requirements
10+ Years
work experience
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