Regulatory Affairs Manager

Job Summary

Reporting to the Director of Regulatory Affairs, the Regulatory Affairs Manager is responsible for executing regulatory strategies, ensuring compliance with global regulations and leading the process to obtain and maintain market approval for DeepHealth’s product and product development and regulatory activities to commercialize new digital products, including AI technologies. This position will provide regulatory input on design and development activities to cross‑functional teams, to ensure compliance with the relevant regulatory requirements and interactions with regulatory authorities.

Essential Duties and Responsibilities

• Oversee the day‑to‑day functions of the US and EU based Regulatory Affairs team members.
• Contribute to and execute the regulatory strategies for existing, new and modified medical and non‑medical devices.
• Represent Regulatory Affairs on cross functional project teams and provide strategic input and technical guidance on product lifecycle planning and regulatory requirements for non‑medical devices, and medical device.
• Leads and manages regulatory submissions, including US 510(k)s submissions, and technical files for CE marking, including Regulatory Body interactions.
• Mentor and provide guidance to their direct reports and cross‑functional product development teams on regulatory requirements, specifically for the US, UK ,and EU markets.
• Work closely with business partners and regulatory team members to ensure compliance for and support of OUS regulatory submissions and filings.
• Monitor and interpret evolving global regulations, standards, and guidance documents to ensure the company’s regulatory compliance, translating them into action steps for the organization.
• Assist in SOP development and review in support of "next-gen" product offerings.
• Create and ensure maintenance of technical documentation (such as clinical evaluation reports, risk management reports, 510(k) notification) as required for obtaining and / or maintaining regulatory approval / clearance for DeepHealth products.
• Evaluate proposed design, labeling, and distribution changes for regulatory impact and implement any required regulatory action.
• Ensure compliance with product post marketing requirements.

PLEASE NOTE : This is not an exhaustive list of all duties, responsibilities and requirements of the position described above. Other functions may be assigned and management retains the right to add or change duties at any time.

Minimum Qualifications, Education and Experience

Physical Demands

This position often requires sitting, standing, walking, bending, twisting, reaching with hands and arms, using hands and fingers, handling, or feeling, speaking, listening, and high-level cognitive thinking. Also, must be able to lift up to 10 pounds occasionally. The position requires the ability to travel (~10% of time), drive a vehicle, and utilize other forms of transportation.

Working Environment

This position may be based in the United States, or the European Union (EU preferred) in a typical office setting. This position will have the ability to work remotely.

ACCOMMODATIONS

Reasonable accommodations may be made to enable people with disabilities to perform the essential functions of the job.

Salary Range

$130K - $150K USD Annually

Notice for New York City Applicants

For roles based in New York City, RadNet / DeepHealth may use an Automated Employment Decision Tool (AEDT) to assist in candidate assessment. New York City residents may review the required AEDT notice, bias audit summary, and information on how to request an alternative process by contacting HR.Support@DeepHealth.com

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