Senior Director, Manufacturing Operations

Immatics US, Inc.; United States; On-site; USD 200,000 - 350,000; Full time

Benefits offered by this job

Health, Dental, and Vision Insurance

4 weeks vacation (pro-rated)

12 company paid holidays

Sick time: 7 days

Life insurance 100% employer-paid

Disability coverage 100% employer-paid

401(k) with company match

Parental leave

Additional voluntary benefits

Job summary

Immatics US, Inc. seeks a Senior Director of Manufacturing Operations to provide strategic and operational leadership for GMP manufacturing and MSAT activities supporting late-stage development, regulatory approval, and commercial supply of cell and gene therapy products.

The role translates CMC strategy into integrated execution across Manufacturing, MSAT, and Digital Manufacturing Systems. Reporting to the Site Head, Immatics US & VP, Technical Operations, this onsite role is based in

Qualifications

• Bachelors degree in a relevant discipline (Immunology, Biochemistry, Cell Biology, Biotechnology, Bioengineering, or Pharmaceutical Sciences).
• 15+ years of progressive Technical Operations or Manufacturing Operations experience including 5+ years direct management in cell therapy manufacturing leadership and strategy in industry setting.
• Masters or Ph.D in a relevant discipline such as Immunology, Biochemistry, Cell Biology, Biotechnology, BioEngineering, or Pharmaceutical Sciences.

Responsibilities

• Lead GMP Operations organization, developing a high-performing team and driving accountability, collaboration, and continuous improvement.
• Provide strategic oversight of GMP manufacturing operations and manufacturing readiness for launches and ongoing supply.
• Oversee process validation, lifecycle management, MSAT activities, technology transfer, and post-approval changes.
• Drive digital manufacturing initiatives, including MES/eBR, automation, and data-driven decision making.
• Ensure alignment with regulatory commitments and GMP requirements; support inspections and compliance.

Education

Bachelor's degree in a relevant discipline (Immunology, Biochemistry, Cell Biology, Biotechnology, Bioengineering, or Pharmaceutical Sciences)

Master's or Ph.D in a relevant discipline such as Immunology, Biochemistry, Cell Biology, Biotechnology, BioEngineering, or Pharmaceutical Sciences

Tools

MES

ERP

LIMS

Statistical process monitoring

Lean Six Sigma

S&OP

Job description

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

The Senior Director, Manufacturing Operations provides strategic and operational leadership for GMP manufacturing and manufacturing sciences activities supporting late-stage clinical development, regulatory approval, commercial launch readiness, and routine commercial supply of cell and gene therapy products. The role translates CMC strategy into integrated execution across Manufacturing, MSAT, Technical Training, Recipe/Document Development, and Digital Manufacturing Systems.

Schedule: Monday-Friday, 1st Shift with weekends and holidays as needed. Reports to: Site Head, Immatics US & Vice President, Technical Operations. Location: Onsite, 13203 Murphy Road Suite 100 Stafford, TX 77477.

Basic Qualifications

• Bachelors in a relevant discipline such as Immunology, Biochemistry, Cell Biology, Biotechnology, Bioengineering, or Pharmaceutical Sciences.
• 15+ years of progressive Technical Operations or Manufacturing Operations experience including 5+ years direct management in cell therapy manufacturing leadership and strategy in industry setting.

Preferred Qualifications

• Masters or Ph.D in a relevant discipline such as Immunology, Biochemistry, Cell Biology, Biotechnology, BioEngineering, or Pharmaceutical Sciences.
• Proven leadership experience supporting late-stage development through commercial manufacturing, including process validation, regulatory submissions, inspection readiness, commercial launch readiness, and ongoing manufacturing operations.
• Deep expertise in cGMP manufacturing, quality systems, and global regulatory requirements for biologics, cell and gene therapy, or other advanced therapy products.
• Demonstrated success leading manufacturing investigations, technology transfers, process validation programs, and cross-functional decision-making to drive compliance, operational excellence, and business objectives.
• Hands-on, visible leader with a strong player-coach mindset. Actively engages with manufacturing operations through routine Gemba presence, team coaching, barrier removal, and rapid resolution of operational, technical, and quality challenges.
• Experience scaling an internal commercial manufacturing organization.
• Experience with MES, ERP, LIMS, statistical process monitoring, Lean Six Sigma, and S&O.P.

In this role you will

Leadership & Organizational Development

Lead, develop, and mentor a high-performing GMP Operations organization, fostering a culture of accountability, collaboration, and continuous improvement. Translate corporate and Technical Operations objectives into integrated operating plans, resource strategies, and measurable performance goals. Build organizational capabilities, develop future leaders, and drive employee engagement across the function. Partner cross-functionally to align priorities, manage risks, and ensure execution against business objectives.

GMP Manufacturing & Commercial Operations

Provide strategic oversight of GMP manufacturing operations, ensuring operational readiness across facilities, personnel, equipment, materials, systems, and processes. Drive safe, compliant, and reliable manufacturing performance through operational excellence, right-first-time execution, and continuous improvement initiatives. Lead commercial manufacturing readiness, product launch activities, capacity planning, and transition to routine commercial supply. Partner with Supply Chain, Quality, Commercial, Clinical Operations, and Patient Operations to establish scalable end-to-end manufacturing and supply processes.

Technical & Process Excellence

Oversee process validation, lifecycle management, process monitoring, and control strategies to ensure a state of continued compliance and operational performance. Lead technology transfer, MSAT activities, technical investigations, process improvements, and post-approval changes. Drive digital manufacturing initiatives, including MES/eBR, automation, manufacturing systems, and data-driven decision making.

Compliance

Ensure alignment between manufacturing operations, regulatory commitments, and GMP requirements. Lead inspection readiness activities and support regulatory inspections, audits, and health authority interactions. Partner closely with Quality and Regulatory Affairs to proactively manage compliance, operational risks, and remediation activities.

Strategic Business Leadership

Establish operational governance through KPI management, performance reviews, risk assessments, and cross-functional decision-making forums. Own operating budgets, headcount planning, capital forecasts, and resource prioritization. Drive cross-functional risk management across quality, supply, capacity, technology, regulatory, and business continuity areas.

Travel Requirements: Occasional; may require travelling domestically or internationally for a conference, business meetings, or corporate retreats.

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.

• 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 and are committed to building a diverse and inclusive workplace. We consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, national origin, ancestry, age, marital status, disability, genetic information, veteran status, or any other status protected by applicable law.

Reasonable Accommodations

We are committed to providing reasonable accommodations to individuals with disabilities and to applicants with sincerely held religious beliefs, practices, or observances. If you require assistance or accommodation during the application or interview process, please contact us at [e-mail].

Work Authorization

Applicants must be authorized to work in the United States without the need for current or future sponsorship.

Pre-Employment Requirements

Employment is contingent upon successful completion of a background check, reference checks and pre-employment drug screening, where permitted by applicable law. For certain roles, additional screenings such as a credit check or motor vehicle record review may be required, where job-related and consistent with business necessity.