Associate Director, CMC Project Management

Scorpion Therapeutics; San Francisco (CA); On-site; USD 150,000 - 230,000; Full time

Job summary

Scorpion Therapeutics in San Francisco is seeking an Experienced Project Manager to lead cross-functional CMC activities for early-stage biopharma development programs, including process development, analytical, quality, regulatory, and supply chain functions.

You will develop integrated project plans, coordinate external partners and CMOs, manage risk, standardize reporting, and support budget planning to ensure successful program execution from early development through late-stage and

Qualifications

• 10+ years in CMC or biotech/pharma functions with at least 5 years in project/program management.
• Strong knowledge of cGMP, quality systems, and regulatory processes.
• Ability to lead complex, multi-stakeholder programs.

Responsibilities

• Lead cross-functional CMC activities across development programs.
• Develop integrated project plans and coordinate external partners and CMOs.
• Support operational excellence and budget planning.
• Manage risk, scenario planning, and reporting processes.
• Ensure program execution from early development through late-stage and regulatory filings.

Skills

Project management

Cross-functional leadership

Risk management

Budget planning

Program coordination

Education

BS/MS in Biotechnology/Chemical Engineering/Biology or related field

Job description

Experienced Project Manager

Leading cross-functional CMC activities for early-stage biopharma development programs, including process development, analytical, quality, regulatory, and supply chain functions. Primary objectives involve developing integrated project plans, coordinating external partners, and ensuring successful program execution from early development through late-stage and regulatory filings. Responsibilities include risk management, scenario planning, standardizing reporting processes, and supporting operational excellence and budget planning. Requirements: BS/MS in Biotechnology, Chemical Engineering, Biology, or related field; 10+ years in CMC or biotech/pharma functions with at least 5 years in project/program management supporting drug development. Proven ability to lead complex, multi-stakeholder programs, with strong knowledge of cGMP, quality systems, and regulatory processes. Preferred qualifications include advanced degrees or certifications (e.g., PhD, MBA, PMP). High-value specifics: supporting early to late-stage development, managing external vendors and CMOs, experience with biologics or infectious disease programs, and working within GxP environments. Work setup: onsite in San Francisco, requiring three days/week presence.