Director, Cell Therapy Manufacturing Operations

Vertex Pharmaceuticals

Boston (MA)

On-site

USD 160,000 - 240,000

Full time

3 days ago
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Benefits offered by this job

Annual bonus
Equity awards

Job summary

Vertex Pharmaceuticals in Boston, MA, seeks an Associate Director, Manufacturing Operations for Cell Therapy to lead a multi-shift manufacturing organization, ensuring compliant production and the development of a high-performing team. The role partners across Vertex to sustain supply of commercial cell therapy products.

The candidate will drive digitization, cost control, and continuous improvement while maintaining regulatory readiness and a strong quality culture.

Qualifications

  • Bachelor's degree in a scientific, technical, or engineering discipline
  • Typically requires 12 years of experience or equivalent combination of education and experience
  • Experience managing day-to-day drug product manufacturing site operations
  • Experience building and training a manufacturing team to operate at a high level in a cGMP environment
  • Experience supporting regulatory inspections (FDA, EMA, and other health authorities)

Responsibilities

  • Deliver compliant, multi-product cell therapy manufacturing operations across three shifts
  • Build and maintain inventory to support patient needs and capacity planning
  • Lead cross-functional teams to translate strategic decisions into manufacturing execution
  • Drive digitization, automation, and data integrity across manufacturing operations
  • Champion GMP compliance and a strong quality culture while developing leaders

Job description

Vertex Pharmaceuticals in Boston, MA, seeks an Associate Director, Manufacturing Operations for Cell Therapy to lead a multi-shift manufacturing organization, ensuring compliant production and the development of a high-performing team. The role partners across Vertex to sustain supply of commercial cell therapy products.

The candidate will drive digitization, cost control, and continuous improvement while maintaining regulatory readiness and a strong quality culture.

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