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About the job

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.

Job Title: Senior Vice President, Technical Operations

Location: This will be a hybrid role, with a weekly in-office requirement of at least 3 days (Monday, Tuesday, Wednesday)

Position summary: The Senior Vice President, Technical Operations will provide leadership and direction for Invivyd’s Technical Operations group. The SVP is responsible for strategy, direction, and execution of technical initiatives in partnership across the organization.

Responsibilities:

Oversee the Technical Operations group including CMC Development, Manufacturing (drug substance, drug product), Supply Chain and Distribution, and Quality Control

Develop and execute Invivyd’s overall clinical and commercial manufacturing strategy including planning, contracting, CDMO oversight, and execution including supply and distribution

Direct CMC development activities including process, analytical and formulation activities for Invivyd’s clinical and commercial product candidates

Provide technical operations oversight for strategic decision making

Lead interactions with CDMOs and other contract services needed to execute the Technical Operations plan and strategy

Provide support and work with other functional areas to develop and communicate the overall corporate strategy

In close coordination with Regulatory Affairs, develop and communicate CMC regulatory strategies to fit the company’s objectives

Represent Invivyd to external audiences, including regulatory authorities and biotechnology industry collaborators/partners

Build strong working relationships across departments to ensure transparency and to facilitate communication

Lead the team through planning for cross-functional transitions

Qualifications:

PhD or equivalent in Biochemical Engineering, Biochemistry or equivalent with biologics including antibody-based development and manufacturing experience

15 years minimum experience in pharmaceutical and/or biotechnology industry, start-up experience is strongly preferred

Multiple years of management experience leading a collaborative team.

Proven success record in overseeing a department, including staffing and budget activities

Experience with biologics development including process, analytical, and formulation development activities

Experience with both early and late clinical stage CMC development required, including validation and commercialization experience

Experience with CDMOs including selection and management; knowledge of cGMPs essential

Experience in a development organization including integration with research, non-clinical, and clinical groups is desirable

CMC regulatory experience essential, including IND / IMPD filings and BLA submissions

Must have excellent leadership and interpersonal skills; should have proven skills as an effective team player who can engender credibility and confidence within and outside the company

Must be science- and data-driven

Pay Range

$304,000- $425,000 The pay range represents the expected full-time base salary for this role at the time of posting. Actual base pay will be determined based on a variety of factors, including relevant experience, skills, and education. In addition to base pay, this role is eligible for both an annual short-term incentive (e.g., bonus or sales incentive) and an annual long-term incentive (e.g., equity), reflecting our commitment to rewarding strong performance and long-term impact. Learn more about our total rewards by visiting https://www.invivyd.com/careers/ .

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.