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• Lead the design of wearable medical devices, ensuring all designs meet companyobjectivesand applicable regulatory requirements; ```{=html}
  
  

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• Maintain a consistent brand identity and visual design language across all company products and interfaces; ```{=html}
  
  

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• Direct design activities to follow regulatory standards, including
  
  

ISO 13485, IEC 62366, ISO 14971:2019, and FDA Human Factors

Engineering Guidance; ```{=html}

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• Prepare documentation to support regulatory submissions, including
  
  

FDA 510(k) and CE MDR filings, human factorsreports, and product risk analyses; ```{=html}

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• Implement andmaintaindesign processes, methods, and workflows to support efficient and compliant wearable medical device development; ```{=html}
  
  

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• Collaborate with regulatory and quality teams to ensure human factors engineering documentation meets submission requirements; ```{=html}
  
  

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• Ensure all design processescomply withoccupational safety, environmental, and manufacturing regulations; ```{=html}
  
  

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• Collaborate with engineering, product development, clinical, and manufacturing teams to incorporate user needs, technical feasibility, and manufacturing considerations; ```{=html}
  
  

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• Support integration of industrial design and UI/UX principles tooptimizeproduct usability, safety, and performance; ```{=html}
  
  

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• Oversee usability testing, iterative prototyping, and evaluations to confirm product design effectiveness and safety; ```{=html}
  
  

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• Supervise a multidisciplinary design team, including product designers, graphic designers, and digital interface designers, overseeing task assignments, workload planning, mentorship, and performance tracking; ```{=html}
  
  

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• Manage administrative functions of the design team, including procurement requests, vendor coordination, and departmental reporting; and ```{=html}
  
  

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• Monitor and analyze industry trends, competitive products, and emerging technologies to drive design innovation andmaintainawareness of best practices.