Director, Manufacturing Technology Lead - Cell Therapy

AstraZenecaLos Angeles, CA
Onsite

About The Position

The Director, Manufacturing Technology Lead reports to the Head of Cell Therapy Manufacturing and is responsible for providing manufacturing operational perspective on new technology evaluation. The role supports full-scale implementation of new technology platforms and advanced automation solutions across the Cell Therapy Manufacturing supply network. This role serves as the critical interface between technology development functions and the manufacturing supply sites, ensuring that operational constraints are understood early and that robust implementation plans enable successful adoption at scale. Additionally, this role supports development of the execution pathway from proof-of-concept completion through validated, GMP-compliant deployment at supply sites.

Requirements

  • Bachelor’s degree in engineering (Mechanical or Robotics), or related discipline
  • Minimum 10 years in manufacturing technology implementation, tech transfer, or engineering
  • At least 5 years leading full-scale technology deployments in regulated environments
  • Strong expertise in at least two of: manufacturing, automation/robotics, AI applications, advanced analytical platforms
  • Practical understanding of moving technology from PoC into validated manufacturing operations
  • Demonstrated track record of leading complex, multi-stakeholder technology implementations from planning through qualification and operational handover in regulated manufacturing environments
  • Experience managing new technology introduction alongside existing operations
  • Execution-oriented leadership
  • Cross-functional collaboration
  • Structured planning
  • Digital and tech savvy
  • The ability to bridge the gap between development innovation and manufacturing operational reality
  • Comfortable operating in a matrixed environment, where, influence and partnership drive outcomes

Nice To Haves

  • Master’s degree preferred

Responsibilities

  • Serve as the primary manufacturing representative in technology evaluation activities led by Process Sciences and Analytical Technology; provide input on operational constraints including facility limitations, operator capability requirements, maintenance complexity, scheduling impacts, and GMP compliance considerations that influence technology feasibility and adoption timelines
  • Evaluate proposed new technologies and platforms against the realities of the manufacturing and quality control environment at supply sites including cleanroom classifications, existing equipment interfaces, material flows, resource models, batch scheduling, and regulatory filing implications
  • Support proof-of-concept evaluations by providing manufacturing perspective on scalability, operability, integration requirements, and implementation risk; ensure PoC success criteria include manufacturing site-relevant parameters
  • Develop detailed implementation plans for adoption of new technology and platforms at manufacturing supply sites, including resource requirements, training needs, validation strategies, execution pathways, site sequencing, and go-live criteria
  • Coordinate technology deployments across the supply network, defining standard implementation playbooks while accommodating site-specific constraints; establish lessons-learned feedback loops to accelerate sequential site deployments
  • Support the development and implementation of the Cell Therapy Technical Operations digital and AI transformation roadmap in collaboration with the Digital and Business Systems teams for new technology
  • Support development of training and competency-building plans that enable operators and engineers to effectively utilize new technologies post-implementation

Benefits

  • Qualified retirement programs
  • Paid time off (i.e., vacation, holiday, and leaves)
  • Health coverage
  • Dental coverage
  • Vision coverage
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