Senior Vice President, Technical Operations

Invivyd

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

Posted 10/6/2026full-timeRemote • United StatesSenior💰 $304,000 - $425,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive expertise in CMC Development, Manufacturing, and Regulatory Affairs within the biotechnology industry, with a strong focus on biologics and a proven track record in leading cross-functional teams and strategic decision-making.

Highest-signal resume keywords

PhD In Biochemical EngineeringBiologics Development ExperienceCMC Regulatory ExperienceLeadership In Pharmaceutical IndustryCDMO Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Process DevelopmentAnalytical DevelopmentFormulation DevelopmentClinical Stage CMC DevelopmentValidation ExperienceCommercialization ExperienceCGMP KnowledgeIND / IMPD FilingsBLA Submissions

Soft Skills

Leadership SkillsInterpersonal SkillsTeam CollaborationCredibility BuildingCommunication Skills

Industry Keywords

Pharmaceutical IndustryBiotechnology IndustryTechnical OperationsSupply ChainQuality ControlContract ManufacturingStrategic Decision MakingCross-Functional Transitions

About the role

Key responsibilities & impact

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 to 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

Requirements

What you’ll need

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 a plus
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