Director, Risk Intelligence and Analytics

What You’ll Do Translate complex technical and regulatory topics into clear executive briefings, highlighting operational implications, risks, opportunities, and required actions. Develop and maintain a forward‑looking risk intelligence landscape scanning process for biopharmaceutical manufacturing, process technology, engineering, GMP expectations, and supply chain resilience; convert insights into decision‑ready recommendations. Lead quantitative and qualitative analyses (trend, scenario, sensitivity, benchmarking) to assess risk and inform network strategy, capacity planning, and manufacturing investments. Build and govern dashboards integrating manufacturing performance, quality, deviations/CAPA, supply, and engineering reliability; ensure data quality, definitions, and traceability. Monitor emerging manufacturing technologies/practices (e.g., digital manufacturing, automation, advanced analytics, continuous manufacturing where applicable) and assess readiness, value, and adoption pathways. Partner with stakeholders to define key questions, prioritize analyses, and align on interpretations and decisions. Develop and deliver executive materials for PO&T leadership (executive summaries, quarterly landscape reports, rapid‑response briefs). Provide analytics and decision support for strategy reviews, business cases, and investment governance (ROI/NPV/IRR, total cost modeling, trade‑off analyses). Establish analytical rigor standards and lead peer review of analyses and narratives. Facilitate cross‑functional workshops to convert insights into plans, owners, and timelines. Continuously improve intelligence/analytics processes (data acquisition, automation, taxonomy, reusable templates). Required Skills / Qualifications Bachelor’s degree and 12+ years in biopharmaceutical technical operations (manufacturing, CMC, manufacturing sciences/quality, engineering, supply chain, regulatory, or operational excellence), including significant analytics experience. Deep understanding of GMP manufacturing operations (batch records, deviations, CAPA, change control, validation) and generated data. Strong knowledge of manufacturing engineering concepts/standards (automation, utilities, maintenance/reliability, process equipment, EHS‑by‑design). Strong knowledge of end‑to‑end supply chain principles and external manufacturing ecosystems (e.g., CMOs), regulatory expectations, and best practices. Ability to synthesize external signals into actionable internal guidance. Proven ability to design and execute analytics strategies (data sourcing, governance, KPI definitions, dashboarding, advanced analysis). Benefits (explicitly listed) Medical, dental, vision, and life insurances; fitness/wellness reimbursement; short‑and‑long term disability. 15+ days paid vacation plus end‑of‑year shutdown (Dec26–Dec31); up to 12 paid holidays + 3 personal days; sick time; paid maternity/parental leave. 401(k) with company match; employee stock purchase plan; tuition reimbursement (up to $10,000/year); Employee Resource Groups participation. #J-18808-Ljbffr Scorpion Therapeutics