Senior Software Engineer

Job Title: Senior Software Engineer

About Satio:

Satio an innovative medical device company, is focused on developing the next generation of vaccine, drug and IVD diagnostic testing platforms. With corporate headquarters in Boston, Massachusetts, Satio attracts and retains exceptional talent with our collaborative culture, passion for our work, and a strong commitment to employee professional development. 

The person will have experience developing innovative and complex software systems in the medical device space, a strong technical foundation in IOS and android device applications as well as cloud-based application development. This top performer that we are looking to bring on board has a demonstrated history of leading product development teams using Agile methodologies to execute on plan, will have great program management skills, and understands how to manage in a fast-paced environment.

The ideal candidate for this highly visible opportunity will have a background in developing medical device software platforms, with expert-level design control, project management, and product development experience.  They must demonstrate an inspirational and collaborative leadership style. This senior-level Engineer will lead complex technical design and development activities, collaborate with senior and junior staff to execute tasks, and coordinate with cross-functional teams to achieve success.

Principal Responsibilities:

• This Senior Software Engineer (Sr Engineer) position will contribute to the design, implementation and verification of software for one or more of the projects we are bringing to market.
• It is a hands-on role that may include all aspects of device software development: firmware and software, algorithm development and optimization, image processing, and application development including knowledge of software architecture including cloud-based architecture.
• Software analysis, planning, design, implementation, and verification of novel medical devices that consists of hardware control, data acquisition, signal/image processing, display, and post processing of medical images.
• Work collaboratively with researchers and application development engineers in all software development phases.
• Design and code medical-grade software that meets the defined software requirements and Design Inputs.
• Thorough knowledge of medical device standards such as IEC62304, ISO14971, IEC60601.
• Create documentation adhering to quality procedures, regulations, standards and industry best practices under Design Control.
• Contribute to product requirement development and risk management reviews.
• Work effectively in cross-functional teams consisting of Research, Engineering, QA/RA, and Marketing.
• Keep abreast of relevant and new technologies in the medical device field.
• Report progress regularly to Management.

Qualifications:

• BS in Systems/Software Engineering or directly related scientific discipline; advanced degree strongly preferred. 
• 5-7 years Software product development experience required.
• Strong preference for experience with class II medical devices.
• Demonstrated history of theoretical and applied understanding of software design.
• Ability to travel up to 20% of the time, domestically & internationally (US & EU).

Location:

• Boston, MA, hybrid in office

Salary:

• $175,000 per year

Relocation Assistance:

• None