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Associate Director, Drug Substance Process DevelopmentInvivyd Inc.New Haven, Connecticut, United States
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Associate Director, Drug Substance Process Development

Invivyd Inc.
  • US
    New Haven, Connecticut, United States
  • US
    New Haven, Connecticut, United States

Über

ABOUT US
There are more than 9 million immunocompromised people in the United States. Almost half a million of those represent a population that are moderately to severely immunocompromised and at highest risk for severe COVID-19, including stem cell and solid organ transplant patients as well as those with hematologic cancers.
At Invivyd, Inc., we take those numbers very seriously and we come to work each day on a mission to deliver protection from serious viral infectious diseases, beginning with SARS-CoV-2. Invivyd deploys a proprietary integrated technology platform unique in the industry designed to assess, monitor, develop, and adapt to create best in class antibodies.
In March 2024, Invivyd received emergency use authorization (EUA) from the U.S. FDA for a monoclonal antibody (mAb) in its pipeline of innovative antibody candidates.
In October 2025, the FDA cleared the company's Investigational New Drug (IND) application and provided feedback to advance the company's REVOLUTION clinical program, Invivyd's development program for VYD2311, a vaccine alternative monoclonal antibody being investigated for the prevention of COVID-19.
Be part of making a difference. Be part of Invivyd.
Location: New Haven (Northeast Preferred)
Position summary:
While the candidate brings strong scientific capability and experience in platform development, their background is primarily focused on early-stage CMC and discovery/preclinical work. This role reports to the Head of Process Development and Manufacturing and is responsible for oversight and execution of drug substance process development activities at Invivyd's Contract Manufacturing Organizations (CMOs), including technology
  • New Haven, Connecticut, United States

Sprachkenntnisse

  • English
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