Senior Systems Engineer
Confirmed live in the last 24 hours
Sibel Health

51-200 employees

Develops flexible sensors for advanced health monitoring
Company Overview
Sibel Health stands out for its commitment to engineering excellence, demonstrated by its development of soft, flexible sensors powered by advanced analytics and cloud integration optimized for AI and machine learning. The company's culture is deeply rooted in inclusivity and global outreach, as evidenced by their mission to provide better health data for all, including those in challenging environments, and their collaboration with professionals and organizations in over 20 countries. This global perspective, combined with their technical prowess, positions Sibel Health as a leader in the health tech industry.
AI & Machine Learning
Data & Analytics

Company Stage

Series B

Total Funding





Chicago, Illinois

Growth & Insights

6 month growth


1 year growth


2 year growth

Chicago, IL, USA
Experience Level
Desired Skills
IT & Security
IT Project Management
System Administration
  • Bachelor's degree in engineering, computer science, or a related technical field.
  • Proven track record of successfully leading complex technical projects in the medical device industry.
  • Strong knowledge of medical device regulations and standards, including FDA and ISO requirements.
  • Ability to lead cross-functional teams and drive results in a collaborative environment.
  • Strong communication skills, with the ability to convey complex technical information to non-technical stakeholders.
  • Ability to work in a fast-paced, dynamic environment and adapt to changing priorities.
  • Collaborate with the Product Management team to define user needs and product requirements and technically meet product manager expectations.
  • Act as a liaison between technical teams and business stakeholders, effectively communicating product requirements and updates.
  • Develop and maintain system requirements and specifications, ensuring alignment between user needs, product requirements, and technical specifications.
  • Collaborate with cross-functional teams including engineering, design, regulatory affairs, quality assurance, and manufacturing to ensure seamless execution of projects.
  • Ensure products meet all relevant regulatory requirements and quality standards. Work closely with regulatory affairs to navigate the approval process.
  • Possess a deep understanding of medical device technologies, industry standards, and regulatory requirements. Stay abreast of emerging trends and technologies in the healthcare space.
  • Stay up-to-date with medical device regulations and standards (e.g., FDA, ISO) and ensure that all products meet or exceed these requirements.
  • Provide subject matter expertise in medical device engineering, including hardware, software, and systems integration. Guide the technical direction of projects, ensuring they meet industry standards and compliance requirements.
  • Identify and mitigate technical risks associated with product development, ensuring that potential issues are addressed proactively.