Jobs · Business Development · Maryland

Associate Director, Global Cell Therapy Sourcing & Procurement

AstraZeneca · Gaithersburg, MD · 3 mo ago
Business Development$116k–$173k/yrFull-time

Responsibilities

  • Lead implementation of category plans to ensure that the underpinning process improvement and procurement activities deliver business value in accordance with the strategic plan and help towards our Sustainability targets.
  • Develop long term strategic plans for agreed scope of spend area, with a focus on delivering broader value, innovation, and savings.
  • Support the team in strategic relationship management (customer and supplier) - ensuring Category Strategies are fully aligned to current and future Business need, and we maintain a supply base capable of supporting these strategies.
  • Work alongside key stakeholders advising on and driving procurement strategies to make decisions necessary to make purchases in congruence with organizational objectives.
  • Advise on contracts and agreements for the supply of sophisticated products and services with new and existing suppliers.
  • Cross functional support of global procurement colleagues and collaborate on setting and completing the strategy.
  • Lead alliance management strategies for key CDMO partnerships.
  • Sourcing and negotiation for Auto TCR-T, Allo CAR-T, and In-vivo manufacturing.
  • Drive COGM reduction initiatives for LVV, Plasmids, Gene Editing, and Drug Product.
  • Build resilient, multi-source supplier base for critical materials in collaboration with technical, quality, and external manufacturing teams.

Requirements

  • Bachelor’s degree or equivalent
  • 7+ years of experience in a procurement environment
  • Significant experience of Category Management (preferably in Cell Therapy)
  • Strong project management, change management and people leadership skills
  • Strong understanding of the pharmaceutical industry
  • Strong communication skills and ability to influence others
  • Comfort with risk and ambiguous situations

Qualifications

  • Proven track record negotiating and managing complex CDMO contracts
  • Technical background (ideally MS&T, CMC, or manufacturing engineering)
  • Strong alliance management skills balancing cost, quality, and relationship dynamics
  • Experience with novel modalities (CAR-T, TCR-T, in-vivo gene editing)
  • Track record managing tech transfers to CDMOs
  • Familiarity with Lean/Six Sigma methodologies
  • China market experience: Deep understanding of China's biotech ecosystem, regulatory environment, and supplier landscape
  • Mandarin language proficiency (for China-focused role)

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