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Engineering Specialist, Software

United States, Round Lake 168000.00 - 231000.00 USD / Year · Job Posted July 14, 2026
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Job Description

This is where your work saves lives. As Technical Specialist, lead the development and execution of product software activities across the global corporation’s medical devices, products, and applications. Be an expert in state-of-the-art software principles, project management, and be able to lead team members in maturing the security position of products. Navigate the balance of security and business needs while focusing on ensuring patient safety. Communicate effectively with both the “doers” and leaders of the organization. Monitor current security industry and regulatory trends to prepare organization for next generation of needs/requirements. Contributes to a software vision that aligns with the organization's vision and strategic plan. Utilizes solid understanding of device and system connectivity concepts in a medical device domain. Provides direction to technical team members that are accountable for implementing cybersecurity, integration, and connectivity deliverables. Exhibits creativity and innovation in completing divisional and cross-functional/business unit goals and objectives.

Job Responsibility

  • Lead execution of software projects across multiple products at all stages of product development, from concept through design, regulatory approval, launch, maintenance, and discontinuation
  • Own software roadmaps and strategic efforts (including sustaining, new product development, and exploratory work)
  • Collaborate with software leaders across the organization to develop, improve, and implement software processes, tools, governance, and best practices
  • Provide technical leadership and development of team members
  • Drive transparent communication about technical risk of product portfolio, identify continuous improvement opportunities, and lead risk reduction efforts
  • Communicate and drive understanding of software health, vulnerabilities, and escalations with business and regulatory leaders
  • Participate in industry activities, staying aligned with and strategically driving guidance and regulations.

Requirements

  • BS in computer science, engineering, mathematics, information management, or related field with 12+ years of industry experience
  • 5+ years of experience in healthcare/medical devices industry
  • Deep understanding of ARM Cortex architectures for embedded systems: bonus points for familiarity with STM32 hardware
  • Subject matter expert knowledge of best practices for software across all stages of product development from concept to production
  • Experience with C/C++, Shell scripting, GitHub configuration management software
  • Experience with software quality related tools such as Coverity, etc.
  • Experience with real-time operating systems (RTOS), specifically FreeRTOS
  • Experience with design control requirements (CFR 820.30, ISO 13485), risk management (ISO 14971), and regulatory guidance
  • Requires strong organization and communication skills, with the ability to interface with both technical and non-technical personnel.

Nice to have

familiarity with STM32 hardware

What we offer

  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • medical and dental coverage that start on day one
  • basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
  • 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
  • Flexible Spending Accounts
  • educational assistance programs
  • paid holidays
  • paid time off ranging from 20 to 35 days based on length of service
  • family and medical leaves of absence
  • paid parental leave
  • commuting benefits
  • Employee Discount Program
  • Employee Assistance Program (EAP)
  • childcare benefits

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