Senior CMC Program Manager

Vir Biotechnology; San Francisco (CA); Hybrid; USD 163,000 - 228,000; Full time

Benefits offered by this job

Health and welfare benefit plans

401K match

Lunch each day in the office

Company shutdown for holidays

Job summary

Vir Biotechnology is seeking an Associate Director of CMC Project Management to lead cross-functional CMC programs from early development through regulatory filings. You will manage integrated project plans, coordinate with external partners, and drive risk mitigation and schedule optimization to accelerate timelines.

This hybrid role is based in San Francisco with three onsite days. Ideal candidates hold a BS/MS in a biotech-related field, 10+ years in CMC/biotech functions, and at least 5

Qualifications

• 10+ years in CMC Development, CMC Regulatory Affairs, Quality, Technical Operations, or related biotech/pharma functions.
• Minimum 5 years of project or program management experience in drug development.
• Strong understanding of cGMP and quality management systems.

Responsibilities

• Lead cross-functional CMC development programs from early-stage to late-stage development and regulatory filings.
• Coordinate external partners, CMOs, and vendors within integrated project plans.
• Drive risk identification, mitigation strategies, and scenario planning to support timelines.

Skills

Cross-functional leadership

Communication

Project management

Risk management

Education

BS or MS in Biotechnology/related field

Tools

PMP

Job description

Vir Biotechnology is seeking an Associate Director of CMC Project Management to lead cross-functional CMC programs from early development through regulatory filings. You will manage integrated project plans, coordinate with external partners, and drive risk mitigation and schedule optimization to accelerate timelines.

This hybrid role is based in San Francisco with three onsite days. Ideal candidates hold a BS/MS in a biotech-related field, 10+ years in CMC/biotech functions, and at least 5