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Regulatory Affairs Manager

Invivyd, Inc.New Haven, CT (Northeast Preferred)
Hybrid Full-time $120K/yr - $160K/yr

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Experience Level

Manager

Qualifications

The Manager, Regulatory will be instrumental in overseeing regulatory activities linked to Invivyd's initiatives. This role includes formulating and implementing regulatory strategies, managing regulatory submissions, and facilitating communications with regulatory authorities. You will collaborate closely with senior management while ensuring compliance and fostering cross-functional teamwork to drive successful outcomes.

About the job

Invivyd, Inc. develops solutions aimed at protecting immunocompromised individuals from severe viral diseases, with a primary focus on SARS-CoV-2. The company’s technology platform supports the creation and refinement of advanced antibodies. In March 2024, Invivyd received emergency use authorization from the U. S. FDA for a monoclonal antibody in its pipeline. By October 2025, the FDA approved the company’s Investigational New Drug application, allowing further clinical development of VYD2311, a monoclonal antibody being studied as a potential alternative to vaccines for COVID-19 prevention.

Location and Work Arrangement

This Regulatory Affairs Manager role is based in New Haven, CT, with a preference for candidates located in the Northeast region. The position offers a hybrid schedule, combining remote work with regular in-office days at Invivyd’s New Haven headquarters.

About Invivyd, Inc.

Invivyd, Inc. is at the forefront of developing solutions for immunocompromised individuals, particularly in response to viral infectious diseases. Our commitment to innovation and excellence drives us to create effective antibodies and strategic partnerships within the healthcare sector.

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