Senior CMC Program Manager

Immatics NV

$120K — $150K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree in life sciences, medicine, immunology, oncology, pharmacy, health sciences, or related field
  • 6+ years of experience in CMC program/project management or complex project leadership in biotech or pharmaceuticals
  • Experience leading cross-functional CMC activities across various departments
  • Academic or industry experience in cell/gene therapy, immunology/oncology, or bioprocessing sciences
  • Strong leadership and stakeholder management ability in fast-paced environments

Responsibilities

  • Develop and maintain comprehensive CMC program plans and timelines
  • Manage CMC deliverables and critical paths to align with development timelines
  • Lead cross-functional CMC meetings and track ensuing action items
  • Foster collaboration across multiple operational teams to optimize efficiency
  • Oversee actions with external vendors and contract manufacturers
  • Support strategic decision-making and planning with senior management
  • Enhance CMC program management tools and operational practices

Benefits

  • Comprehensive health, dental, and vision insurance
  • Generous vacation policy with 4 weeks granted upfront
  • 12 paid company holidays
  • 7 days of sick leave annually
  • 100% employer-paid life insurance and disability coverage
  • 401(k) plan with significant employer matching
  • Partially paid parental leave for eligible staff
  • Optional employee-paid benefits like accident and theft protection
Full Job Description
Role Overview:

We are seeking a Senior Program Manager, CMC to lead and coordinate cross-functional Chemistry, Manufacturing, and Controls (CMC) activities within a cell therapy development and manufacturing environment. The Senior 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: Senior Director
Location: 13203 Murphy Road Suite 100 Stafford, TX 77477

Basic Qualifications:
  • Master's degree in life sciences, medicine, immunology, oncology, pharmacy, health sciences, or a related field
  • 6+ years of experience in CMC program/project management or complex project leadership within biotechnology, pharmaceutical, or oncology-focused clinical development environments
  • Demonstrated experience leading cross-functional CMC activities, including manufacturing, quality, analytical, and regulatory operations
  • Academic or industry experience in cell and gene therapy, immunology/oncology, or bioprocessing/manufacturing sciences
  • Proven leadership, stakeholder management, and organizational skills with the ability to manage competing priorities in fast-paced environments


Preferred Qualifications:
  • 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 complex programs and critical paths across multiple technical and operational functions
  • Proficiency with project management tools, dashboards, and reporting systems in regulated environments
  • Advanced 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?

At Immatics, we believe in investing in our team's health, safety and well-being. Here's what you can expect if you join Immatics

Comprehensive Benefits:
  • 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.

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