Senior Director, Next Gen Car-t Quality Leader

Johnson & Johnson MedTech

Malvern, Pennsylvania, United States of America
Not specified (assumed to be hybrid based on industry standards).
Car-t manufacturing quality strategy
Cgmp regulations and standards
Quality management systems
Johnson & Johnson MedTech is seeking a Senior Director, Next Gen CAR-T Quality Leader to oversee the Quality strategy for their innovative cell therapy manufacturing process. The role requires extensive experience in Quality Assurance, particularly in biologics and CAR-T manufacturing, and offers the opportunity to lead a global team while fostering a culture of excellence

Job Summary

  • This strategic Quality leadership role is responsible for shaping, executing, and overseeing the end-to-end Quality strategy for Johnson & Johnson’s next-generation CAR-T manufacturing and QC testing platform.
  • The role serves as the primary platform Quality responsible leader, accountable for end-to-end Quality oversight from clinical development through full commercial launch of two global manufacturing locations.
  • This leader will manage a global team of QA & QC professionals, fostering a culture of excellence and continuous improvement.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Senior Director, Next Gen CAR-T Quality Leader to oversee the Quality strategy for their innovative cell therapy manufacturing process. The role requires extensive experience in Quality Assurance, particularly in biologics and CAR-T manufacturing, and offers the opportunity to lead a global team while fostering a culture of excellence.

Skills & Requirements

Must-have

  • CAR-T manufacturing quality strategy
  • cGMP regulations and standards
  • Quality Management Systems
  • cell therapy manufacturing
  • global health authority regulations

Nice-to-have

  • strategic leadership
  • transformational change
  • inclusive leadership
  • continuous improvement mindset
  • advanced Quality capabilities

Key Requirements

  • Bachelors degree in Pharmacy, Engineering, Chemistry, Microbiology or related scientific / engineering discipline
  • At least 12 years working experience in the pharmaceutical industry
  • Minimum of 12 years of Quality Assurance experience related to manufacturing
  • Experience launching facilities is required
  • Fluent in English, written and spoken

Work Rights

Not specified

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