R&D Engineer

Job Title : R&D Engineer (Contract to Permanent) Location :
Andover, MA;
Onsite (No Remote or Hybrid) Type:
Contract (3 to 6 months), with conversion to permanent based on performance Company Overview :

At Digital Health Solutions, we specialize in developing and supporting next-generation medical technologies — from embedded systems and connected mobile apps to cloud platforms, regulatory strategy, and contract manufacturing. As an ISO 13485-certified partner, we work with innovators building Class I–III medical devices, SaMD, and connected digital health solutions.

We are hiring an entry level R&D Engineer to support active medical device product development projects. You will work directly with senior engineers across electrical, firmware, and systems disciplines, gaining hands on exposure to FDA regulated product development. This is a contract to permanent position. Conversion to permanent is based on demonstrated performance rather than a fixed calendar date.

• Assist with circuit design validation and prototype testing.
• Analyze and interpret electrical schematics and PCB layouts under senior engineer guidance.
• Support component sourcing, procurement, and BOM management for prototypes and production builds.
• Troubleshoot hardware and firmware integration issues using laboratory instrumentation and debugging tools.
• Develop and maintain test fixtures.
• Perform prototype assembly and manufacturing support tasks as assigned.
• Execute test protocols and document results in support of verification and validation.
• Conduct testing activities and collaborate with engineering teams to evaluate device performance and functionality.
• Document test results, design changes, and engineering findings in compliance with design control procedures.
• Collaborate with senior engineers and quality staff across multiple concurrent client programs.

• Bachelor's degree in Electrical Engineering, Computer Engineering, Biomedical Engineering, or a closely related field, completed prior to start date.
• 0-2 years of professional, coop or internship experience in hardware, firmware, or device development.
• Coursework and knowledge of microcontroller platforms and embedded systems fundamentals.
• Strong written communication skills, since documentation is a core part of regulated device work.
• Willingness to work onsite in Andover and learn across disciplines rather than specialize immediately.
• Must be authorized to work in the United States or willing to accept visa sponsorship upon conversion to permanent.

• Coursework or project experience involving medical devices or regulated products.
• Exposure to equipment such as oscilloscopes, multimeters, or logic analyzers.
• Familiarity with version control and basic scripting.

• Competitive hourly rates
• Hands on mentorship from senior engineers across mechanical, electrical, firmware, and quality disciplines.
• Real exposure to active FDA submission work rather than simulated projects.
• A clear, performance based path from contract to permanent role.
• Small company visibility, including direct access to company leadership