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)