CMC Program Manager, Cell Therapy & Cross-Functional Lead

Immatics N.V.; Houston (TX); On-site; USD 150,000 - 210,000; Full time

Benefits offered by this job

Health insurance

Vacation days

Holidays

Disability coverage

401(k) match

Parental leave

Job summary

Immatics US is seeking a Program Manager, CMC to lead cross-functional activities in a cell therapy development and manufacturing setting. You will coordinate planning, execution, and integration across manufacturing, analytical, quality, regulatory, and supply chain to support clinical development and commercialization goals.

This role reports to the Director of Program Management and is based at our Stafford, TX location, requiring collaboration with multiple internal teams and external

Qualifications

• Bachelor's degree in life sciences or related field.
• 5+ years in biotech/pharma/oncology clinical development.
• Demonstrated experience in CMC programs and cross-functional work.
• Academic or industry experience in cell/gene therapy, immunology/oncology, or bioprocessing.

Responsibilities

• Develop and maintain CMC program plans, timelines, risk registers, trackers, and reporting tools.
• Manage CMC deliverables, milestones, and critical paths.
• Lead cross-functional CMC meetings including agenda setting and action tracking.
• Drive collaboration across Manufacturing, Process Development, Analytical Development, Quality, Regulatory, Supply Chain, and Patient Operations.
• Coordinate and oversee activities with external vendors, CMOs, CDMOs.
• Support strategic governance and senior management decision-making.
• Contribute to continuous improvement of CMC tools and onboarding processes.

Skills

CMC programs

Cross-functional leadership

Regulatory operations

Education

Bachelor's degree in life sciences

Advanced degree (Masters/PhD)

Job description

Immatics US is seeking a Program Manager, CMC to lead cross-functional activities in a cell therapy development and manufacturing setting. You will coordinate planning, execution, and integration across manufacturing, analytical, quality, regulatory, and supply chain to support clinical development and commercialization goals.

This role reports to the Director of Program Management and is based at our Stafford, TX location, requiring collaboration with multiple internal teams and external