Posted:
7/31/2024, 8:34:29 AM
Location(s):
Northeast, Vietnam
Experience Level(s):
Expert or higher ⋅ Senior
Field(s):
Legal & Compliance
Workplace Type:
Hybrid
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. Our proprietary INVYMAB™ platform approach combines state-of-the-art viral surveillance and predictive modeling with advanced antibody engineering, designed to facilitate the rapid, serial generation of new monoclonal antibodies (mAbs).
Join an incredible team of innovators, disrupters, predictive modelers, and antibody engineers who embrace a shared sense of ownership, a passion to save lives, think boldly and creatively, take targeted risks, are unafraid of failure, and welcome change as a positive catalyst to new opportunities.
This is your chance to be part of the company with the first mAb authorized in over a year and the only one currently on the market for pre-exposure prophylaxis of COVID-19 in certain adults and adolescents (12 years of age and older weighing at least 40 kg) with moderate-to-severe immune compromise.
Be part of making a difference. Be part of Invivyd.
Invivyd has an exciting opportunity to join the team as our Senior Vice President Regulatory Affairs and Quality Assurance. This critical leader and member of our Executive Leadership Team will drive all facets of Invivyd’s regulatory and clinical quality assurance functions. This includes regulatory strategy, leading interactions with clients and global regulatory submissions, representing Invivyd in front of the FDA, EMA, and other regulatory authorities, ensuring close collaboration with CMC, Quality and Clinical teams, as well as external consultants and collaborators, as needed.
Responsibilities:
Requirements:
At Invivyd we strive to create a welcoming and inclusive environment. Here all applicants will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics.
Invivyd is proud to be an equal opportunity employer.
We do not accept unsolicited resumes from agencies.
Website: https://invivyd.com/
Headquarter Location: Waltham, Massachusetts, United States
Employee Count: 101-250
Year Founded: 2020
IPO Status: Public
Last Funding Type: Series C
Industries: Biotechnology ⋅ Pharmaceutical ⋅ Therapeutics