At Withings, we are driven by a mission to empower people to take control of their health.

We are passionate about designing products that are not only innovative but also thoughtfully designed and intuitive to use. Our connected scales, hybrid watches, blood pressure monitors, sleep trackers, and other devices are trusted by millions of users worldwide for seamless integration into their daily lives.

Our vision is to revolutionize healthcare through prevention, early detection, and support for chronic diseases. By combining cutting-edge technology with user- friendly design, we are transforming the way individuals monitor and manage their health.

To maintain the highest standards of innovation and compliance, we are seeking a US RA Manager to join our Quality and Regulatory Affairs team.

Missions

• Provide management and leadership to the Regulatory Affairs organization in the development and implementation of regulatory strategies and processes to gain product approvals in the US market.
• Expert knowledge of clinical development within US and Global regulatory strategy.
• Support in clinical studies required for regulatory approvals, including clinical study design, data analysis, and data reduction.
• Represent as main point-of-contact for the FDA, managing communications, meetings, and document submissions (e.g., 510(k), PMA, IDE, etc.).
• Oversee the preparation and submission of regulatory filings, ensuring timely and accurate submissions to the FDA and other authorities.
• Provide overall review, day-to-day management and operational success for all regulatory functions including the successful integration of activities cross-functionally.
• Assist the team, provide training and interpretations of FDA.
• Ensure that all products comply with US regulatory requirements, including safety, efficacy, and labeling standards.
• Monitor changes in regulatory guidelines and communicate impacts to the broader team.
• Manage reporting and addressing adverse events, recalls, or other compliance-related matters.
• Conduct and oversee FDA inspections and internal audits in compliance with 21 CFR requirements.
• Update procedures and quality documentation as necessary to ensure alignment with FDA regulations.

• Support the planning and execution of market entry strategies for new products in the US, including regulatory approvals and clearances.