Software Engineer

Indianapolis, IN

About SonaCare Medical:

SonaCare Medical is a world leader in minimally invasive focused ultrasound (HIFU) technologies. SonaCare Medical is committed to developing focused ultrasound related technologies that support precise and innovative procedures for the treatment of a range of medical conditions. SonaCare Medical, with its subsidiary Focus Surgery, Inc., designs and manufactures medical devices, including the following: Sonablate®, which has 510(K) clearance in the U.S. under a De Novo regulatory classification; Sonablate® 500, which has CE Marking and has obtained regulatory authorization in more than 49 countries outside the U.S.; Sonatherm® laparoscopic HIFU surgical ablation system, which has 510(K) clearance in the U.S., has CE Marking and has obtained regulatory authorization in more than 30 countries outside the U.S.

Summary: 

The Software Engineer is responsible for the development of ultrasound medical device software to support current and future company products and will participate in the manufacturing, testing, servicing, and documentation of products.

Duties and Responsibilities:

  • Design, develop and test medical device software.
  • Develop and maintain software documentation, including test protocols.
  • Provide front-line IT support.
  • Serve as investigator or contributor for assigned feedback and complaint investigations..
  • User interface development.
  • All other duties, as assigned.

Qualifications/Specifications:

  • Bachelor’s degree in Computer Science, required.
  • 5+ years of experience with coding and software testing, required.
  • Excellent communications skills, required. Proficient in English, both verbal and written.
  • Experience on hardware/software development teams.
  • Experience with Java, C++, and Swing.
  • Experience with Windows and Linux.
  • Experience with build scripting/build management, preferred.
  • Working knowledge of software development in a highly regulated environment, preferred (FDA Quality System Regulation, ISO 13485, other regulations and industry standards regarding clinical research and regulation of medical devices
  • Experience successfully working as part of a cross-functional team, required.
  • TCP/IP interfaces and HTML - design protocols experience, preferred.
  • General knowledge of IEC 62304 Medical Device Software –Software Life Cycle Processes, preferred.
  • Programming embedded systems and Microcontrollers, preferred
  • Hardware interfacing and interfacing protocols experience, preferred (Serial, Parallel, USB, USB2, USB3, VXI, GPIO, I2C, etc.)
  • Experience with OpenGL (3D modeling), preferred.

 

 

 

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HIFU company

Contact

10130 Perimeter Pkwy, Suite 250
      Charlotte, NC 28216

(888) 874-4384

info@SonaCareMedical.com

Mon - Fri: 9:00 - 5:00

Latest News

26 September 2017

Medicare recognizes HIFU prostate ablation as a device-intensive procedure driving new ASC payment going into effect on or after October 1, 2017 CHARLOTTE, N.C., Sept. 20, 2017 /PRNewswire/ -- SonaCare...

29 August 2017

CHARLOTTE, N.C., August 30, 2017 – SonaCare Medical, the leading developer and manufacturer of high intensity focused ultrasound (HIFU) technologies, announces today the successful collaboration with BK Ultrasound, achieving compatibility...