Senior Director, GMP Manufacturing Operations

Immatics

Stafford (TX)

On-site

USD 250,000 - 320,000

Full time

6 days ago
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Benefits offered by this job

Comprehensive Benefits
Health, Dental, Vision Insurance
401(k) with company match
Parental leave

Job summary

Immatics in Stafford, TX is seeking a Senior Director, Manufacturing Operations to provide strategic and operational leadership for GMP manufacturing and MSAT activities supporting late-stage development and commercial supply of cell and gene therapies. The role emphasizes cGMP compliance, tech transfer, process validation, and digital manufacturing initiatives (MES, ERP, LIMS).

You will lead a high-performance team, manage budgets, and partner across Quality, Regulatory, Supply Chain, and

Qualifications

  • 15+ years in Technical Operations or Manufacturing Operations
  • 5+ years direct management in cell therapy manufacturing leadership
  • Deep expertise in cGMP manufacturing, quality systems, and global regulatory requirements
  • Experience with process validation programs and tech transfers
  • Hands-on leader with team coaching and barrier removal

Responsibilities

  • Lead GMP Operations organization and drive accountability
  • Translate objectives into operating plans and measurable goals
  • Oversee manufacturing readiness across facilities, equipment, and systems
  • Drive product launch readiness and capacity planning
  • Lead technology transfer, MSAT activities, and investigations
  • Ensure compliance and inspection readiness across quality and regulatory

Skills

GMP Operations
Manufacturing Leadership
Cell Therapy
cGMP
Regulatory Submissions
Process Validation
MSAT
Lean Six Sigma

Education

Bachelor’s in Immunology/Biochemistry/Cell Biology
MS/PhD in relevant field

Tools

MES
ERP
LIMS

Job description

Immatics in Stafford, TX is seeking a Senior Director, Manufacturing Operations to provide strategic and operational leadership for GMP manufacturing and MSAT activities supporting late-stage development and commercial supply of cell and gene therapies. The role emphasizes cGMP compliance, tech transfer, process validation, and digital manufacturing initiatives (MES, ERP, LIMS).

You will lead a high-performance team, manage budgets, and partner across Quality, Regulatory, Supply Chain, and

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