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Empatica

AI-enabled medical wearables for remote monitoring

Quality Assurance Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeMilan, Metropolitan City of Milan, Italy

About the Job

Requirements

  • A strong academic background, with a BS or MS in Biomedical Engineering.
  • At least 3 years of experience as a Quality Assurance Specialist, Design Quality Engineer, Quality Engineer, or similar role in a company that designs or manufactures medical devices.
  • Knowledge and experience working with ISO standards, including ISO 13485 and ISO 14971.
  • Knowledge and experience working with IEC standards, including IEC 60601 and IEC 62304.
  • Knowledge of MDR 2017/745.
  • Native English proficiency or at least 3 years of work experience conducted in English.

Responsibilities

  • Champion quality culture and compliance within development teams, supporting their compliance efforts.
  • Continually drive improvements in product and process quality.
  • Provide quality and independent review at defined design reviews, design plans, risk management activities, design verification and validation protocols and reports for new development projects and design or process changes to existing products.
  • Support the team in performing required risk management activities.
  • Support the engineering manager with change management and new product development activities, and support developers in creating design control documentation while ensuring product and regulatory requirements are aligned.
  • Support design transfer activities to ensure quality compliance of the manufacturing process.
  • Interface with Regulatory Affairs, Clinical Science, Marketing, and the product manager to translate their needs into actionable, regulatory-compliant requirements.
  • Implement, maintain, and update procedures to ensure the design control process consistently meets company and regulatory requirements.
  • Support Regulatory Affairs in drafting EU technical documentation and US 510(k) and De Novo submissions.
  • Ensure production activities comply with internal procedures and internationally applicable standards.
  • Keep up to date on ISO, EN, FDA, MDR, and other product-development regulatory requirements, and relay this information to the Product Development group.

About the Company

Empatica

AI-enabled medical wearables for remote monitoring

Empatica creates AI-enabled wearable devices and accompanying software for remote patient monitoring and health research. Its medical-grade wearables continuously collect physiological and behavioral data in real time, which can be analyzed to monitor conditions, forecast potential health issues, and support research projects. The devices and subscription-based software work together: hardware collects data from sensors and the software analyzes it with AI to provide actionable health insights, alerts, and trends for patients, clinicians, and researchers. The company differentiates itself by offering clinically validated hardware and a platform that integrates data collection with ongoing software services, serving universities, hospitals, companies, and charities. Its goal is to provide reliable, real-time health information that helps improve patient care, advance medical research, and enable proactive health management.

Company size
51-200
Company stage
Series B
Total funding
$36.3M
Headquarters
Milan, Italy
Founded
2011

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