CMC Program Manager

Immatics US

Georgia

On-site

USD 140,000 - 190,000

Full time

7 days ago
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Benefits offered by this job

Health insurance
Vacation time
Holidays
Sick time
Life insurance
Disability insurance
401(k) match
Parental leave
Additional voluntary benefits

Job summary

Immatics US is seeking a Program Manager, CMC to lead cross-functional Chemistry, Manufacturing, and Controls activities within a cell therapy development and manufacturing environment. You will drive planning, execution, and alignment across manufacturing, analytical, quality, regulatory, and supply chain to support clinical and commercial goals.

This role reports to the Director of Program Management and requires strong leadership, risk management, and communication to coordinate internal

Qualifications

  • Bachelor's degree in life sciences or related field.
  • Experience in biotechnology/pharma clinical development, especially CMC.
  • Background in cell and gene therapy, immunology, or bioprocessing is preferred.

Responsibilities

  • Develop and maintain CMC program plans, timelines, risk registers, trackers, and reporting tools.
  • Manage CMC deliverables and milestones aligning with development timelines.
  • Lead cross-functional CMC meetings and coordinate with external vendors/CDMOs.

Skills

CMC program management
Cross-functional leadership
Project management
Regulatory submissions
Cell & gene therapy
Communication skills
Vendor coordination

Education

Bachelor's degree in life sciences
Advanced degree (Masters/PhD)

Tools

PM dashboards

Job description

Join Immatics and shape the future of cancer immunotherapy; one patient at a time!

Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME , a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics.

Why Join Us?

Innovative Environment: Help to pioneer advancements in cancer immunotherapy.

Collaborative Culture: Be part of a diverse team dedicated to your professional growth.

Global Impact: Contribute to therapies that make a lasting impact on patients globally.

Role Overview

We are seeking a Program Manager, CMC to lead and coordinate cross-functional Chemistry, Manufacturing, and Controls (CMC) activities within a cell therapy development and manufacturing environment.

The Program Manager, CMC will drive planning, execution, and integration across manufacturing, analytical, quality, regulatory, and supply chain functions to support clinical development and commercialization goals. This role serves as a strategic partner across technical and operational teams, ensuring alignment, proactive risk management, and readiness for key milestones, including regulatory submissions and commercial manufacturing.

Reports to : Director, Program Management

Location : 13203 Murphy Road Suite 100 Stafford, TX 77477

Basic Qualifications
  • Bachelor's degree in life sciences, medicine, immunology, oncology, pharmacy, health sciences, or a related field
  • 5+ years of experience within biotechnology, pharmaceutical, or oncology-focused clinical development environments
  • Demonstrated experience in CMC programs and projects working cross-functionally within CMC activities, including manufacturing, quality, analytical, and regulatory operations
  • Academic or industry experience in cell and gene therapy, immunology/oncology, or bioprocessing/manufacturing sciences
Preferred Qualifications
  • Advanced degree such as a Masters or PhD in life sciences, medicine, immunology, oncology, pharmacy, health sciences, or a related field
  • Experience supporting late-stage CMC programs in immunology, oncology, or cell and gene therapy
  • Proven experience managing programs and critical paths across multiple technical and operational functions
  • Proficiency with project management tools, dashboards, and reporting systems in regulated environments
  • Proven leadership, stakeholder management, and organizational skills with the ability to manage competing priorities in fast-paced environments
  • An ability to identify risks, drive decision-making, and implement process improvements across cross-functional teams
  • Experience coordinating external vendors, CMOs, CDMOs, or consulting partners
  • Strong communication and presentation skills with experience supporting senior leadership discussions and strategic planning
In this role you will:
  • Develop and maintain CMC program plans, timelines, risk registers, trackers, and reporting tools to support integrated program execution
  • Manage CMC deliverables, milestones, and critical paths while ensuring alignment with overarching development program timelines
  • Lead and facilitate cross-functional CMC meetings, including agenda development, documentation, action tracking, and follow-up activities
  • Drive collaboration across Manufacturing, Process Development, Analytical Development, Quality, Regulatory, Supply Chain, and Patient Operations teams
  • Coordinate and oversee activities with external vendors, contractors, CMOs, and CDMOs
  • Support strategic planning, governance, and decision-making activities with department leaders and senior management
  • Contribute to continuous improvement of CMC program management tools, processes, onboarding, and operational best practices
What do we offer?
  • Competitive rates for Health, Dental, and Vision Insurance
  • 4 weeks of vacation, granted up front each year and prorated for first and last year of employment.
  • 12 company paid holidays
  • 7 days of sick time
  • 100% employer-paid life insurance up to at 1x annual salary, up to one hundred thousand dollars
  • 100% employer-paid short- and long-Term disability coverage
  • 401(k) with immediate eligibility and company match. The company will match 100% of your contributions up to 3% of your base salary for the first two years of employment, 4% for years 2-3 of employment, and up to 5% of your salary from the fourth year onward of continued employment.
  • Partially paid parental leave for eligible employees.
  • Additional voluntary employee-paid benefits and services, including accident, hospital indemnity, and critical illness insurance, as well as identity theft protection and pet insurance.
Equal Employment Opportunity

We are an equal opportunity employer

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