Key Duties and Responsibilities:
- Design, implement, and maintain manufacturing oversight systems for clinical and commercial supply.
- Integrate operational, engineering, and scientific data into actionable insight.
- Collaborate globally to improve operational efficiency in CMC and manufacturing planning, forecasting, and execution.
- Monitor and implement fast-moving AI technologies and regulatory trends; build and maintain compliant system capabilities.
- Execute timely technology/AI/data activities to required quality standards.
- Collaborate cross-functionally to understand needs and deliver to value.
- Travel up to 10% to support business objectives.
Knowledge and Skills:
- Experience designing and implementing data/technology solutions across clinical/commercial manufacturing networks.
- Strong analytical/problem-solving skills; ability to use data to inform decisions.
- Excellent written/verbal communication; present complex technical concepts to diverse audiences.
- Strong commitment to compliance and integrity in biotech systems/processes.
- Proficiency adopting emerging technologies (e.g., agentic).
- Proficiency with manufacturing software/tools and understanding manufacturing processes.
Education and Experience:
- Bachelorβs in supply chain/logistics, computer science, IT, or equivalent; Masterβs preferred.
- 5+ years in technology (ideally supply chain or project management).
- Cross-functional collaboration experience.
- Proven track record implementing/optimizing digital systems and data flows.
- Regulatory/industry standards experience, including GxP.
- Experience with supply chain processes across modalities (small molecule, cell therapy, gene therapy).
- AI/ML and data engineering strategies highly desirable.
- Advanced certifications in product/agile/software engineering/cloud/leadership preferred.