Careers

Description:

At Suntra we take products from concept to market, with a portfolio spanning life-sustaining pumps, surgical robots, and guidance systems, in-vitro and in-vivo diagnostic devices, 3D imaging systems, insulin and infusion pumps, wearable monitors with connectivity to mobile apps and cloud databases/web interfaces, and much more.

We are seeking a Program Manager with a background in software and hardware development to lead teams developing software and electromechanical systems for medical products. Our programs can include combinations of embedded, desktop, web, mobile, and cloud software as well as complex electromechanical devices. We will look for your experience implementing and leading software/firmware/hardware projects from concept to production. You will stand out with a background developing software/firmware for medical devices.

At Suntra You Will:

• Manage all activities of the project team, ensuring that all contract deliverables and product/project requirements are being fulfilled, including schedules and budgets
• Lead teams of highly skilled software engineers coding in a range of programming languages and environments, including C/C++, C#, Qt, Python, and more
• Lead teams of engineers developing electrical and mechanical solutions to complex problems
• Be the lifeline to our clients, responsible for understanding their needs, technical requirements, and schedule; generating project plans and documentation that include accurate requirements and scope definitions.  You will identify project risks and mitigations, and be the primary point of contact for customer communications

We’re Looking For:

• Exceptional planning and organizational skills, with the ability to manage multiple projects concurrently, and a deep understanding of Agile-based software development
• Strong knowledge of current technologies, tools, automation, and processes
• Aptitude for leveraging AI tools (Cursor AI, CoPilot, etc.) for software and product development
• Working knowledge of FDA regulations and international standards related to the medical device industry including design controls for FDA Class II/III products
• Strong presentation, interpersonal, communication, follow-through, and organizational skills
• 5-10 years of software development project management experience in a medical device environment
• BS in engineering with software/firmware background
• Hybrid work environment, onsite 3-4 days a week

You Will Stand Out With:

• Familiarity with embedded, mobile, cloud, and client-server architecture and database development
• Direct engineering experience developing hardware or software
• Experience in an engineering services environment
• Customer-focused attitude

Why work with us:

• A comprehensive benefits package including Health Insurance with 100% company-paid Dental, Life and Disability insurance
• Three weeks’ vacation, unlimited sick time, plus10 paid holidays 
• Monthly lunches and socials, “Bagel Tuesday” 
• Hybrid work environment

At Suntra MedTech Solutions, we’re driven by a simple but powerful idea: to make a measurable difference in patients’ lives by partnering with medtech companies to bring life-changing technologies to market. Formerly known as Sunrise Labs, we’ve spent over 30 years building a reputation for excellence. Now, as Suntra, we’re expanding that legacy with a broader, more integrated approach.

Our teams work at the intersection of consulting, engineering, and innovation, helping clients solve complex challenges from the earliest spark of an idea through to commercial readiness. Whether we’re uncovering strategic gaps, scaling an established pipeline, or designing with patients and providers in mind, we do it with rigor, heart, and purpose.

If you want to work where your expertise is valued, your curiosity is encouraged, and your work has real-world impact, Suntra is the place to grow. We’re building the future of medtech—come help us lead it.

We’re in southern New Hampshire where the mountains, lakes, and oceans are our playground, and Boston is just down the road. We offer great benefits and competitive salaries based on experience.

We do not accept resumes from staffing agencies or search firms unless a valid search agreement is in place with the agency for a specific position.

Responsibilities:

• Lead the design, development, and integration of complex mechanical components, mechanisms and assemblies for medical devices.
• Own product development activities from concept through commercialization, including requirements definition, feasibility studies, design, prototyping, verification, and transfer to manufacturing.
• Apply knowledge of materials, manufacturing processes (e.g., injection molding, machining, extrusion), and tolerance analysis to ensure robust, cost-effective designs.
• Perform risk analysis, design reviews, and FMEA to ensure compliance with regulatory standards (ISO 13485, FDA 21 CFR Part 11, IEC 60601, etc.).
• Create and maintain detailed engineering documentation including CAD models, drawings, and design history files (DHFs).
• Collaborate with cross-functional teams (electrical systems, software, quality, manufacturing, regulatory) to deliver integrated solutions.
• Provide technical mentorship and guidance to junior engineers and interns.
• Stay current with industry trends, regulatory requirements, and emerging technologies relevant to medical devices.

We’re Looking For:

• Education: B.S. or M.S. in Mechanical Engineering or related discipline.
• Experience: 7–10 years of hands-on product development experience, with at least 5 years in the medical device or regulated industry.
• Proven track record of bringing products from concept to market.
• Strong proficiency in 3D CAD (e.g., SolidWorks) and PDM systems.
• Deep understanding of design for manufacturability (DFM), design for assembly (DFA), and GD&T.
• Experience of mechanisms (kinematics, dynamics, machine design)
• Familiarity with human factors engineering, usability, and biocompatibility considerations.
• Knowledge of verification testing methods and reliability engineering.
• Excellent problem-solving, analytical, and communication skills.
• Ability to work independently and lead cross-functional design efforts.

Preferred Skills:

• Experience with Class II or Class III medical devices.
• Experience with fluidics, micro-mechanics, or disposable device design.
• Hands-on prototyping and test fixture development.
• Exposure to project management tools and agile product development methodologies.

Why work with us:

• A comprehensive benefits package including Health Insurance with 100% company-paid Dental, Life and Disability insurance
• Three weeks’ vacation, unlimited sick time, plus10 paid holidays 
• Monthly lunches and socials, “Bagel Tuesday” 

At Suntra MedTech Solutions, we’re driven by a simple but powerful idea: to make a measurable difference in patients’ lives by partnering with medtech companies to bring life-changing technologies to market. Formerly known as Sunrise Labs, we’ve spent over 30 years building a reputation for excellence. Now, as Suntra, we’re expanding that legacy with a broader, more integrated approach.

Our teams work at the intersection of consulting, engineering, and innovation, helping clients solve complex challenges from the earliest spark of an idea through to commercial readiness. Whether we’re uncovering strategic gaps, scaling an established pipeline, or designing with patients and providers in mind, we do it with rigor, heart, and purpose.

If you want to work where your expertise is valued, your curiosity is encouraged, and your work has real-world impact, Suntra is the place to grow. We’re building the future of medtech—come help us lead it.

We’re in southern New Hampshire where the mountains, lakes, and oceans are our playground, and Boston is just down the road. We offer great benefits and competitive salaries based on experience.

We do not accept resumes from staffing agencies or search firms unless a valid search agreement is in place with the agency for a specific position.