Associate Director, Evaluation and Quality Standards
Publicado en 2026-09-30
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TI/Tecnología
Evaluación de IA, Ingeniero de IA
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
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As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Data Science
Job Category:
People Leader
All Job Posting Locations:
Cornellà de Llobregat, Barcelona, Spain, Madrid, Spain
Evaluation & Quality Standards to join our Data Science and Digital Health team (DSDH). This is a newly created leadership role within the Generative AI organization, reporting directly to the Head of Generative AI. The GenAI team is deploying AI across discovery, development, regulatory, and operations to create AI assistants and agentic systems across the therapeutic areas and functions.
As we scale from proof-of-concept to enterprise deployment, we need a dedicated evaluation function that defines what quality means for generative AI in a regulated pharmaceutical R&D environment, communicates the metrics effectively, and enforces that standard across every platform, vendor, and capability we build or adopt.
This role owns evaluation and governance for all generative AI work across R&D.
Key Responsibilities- Design and maintain evaluation frameworks for GenAI solutions spanning LLM quality, RAG performance, agent reliability, safety, and scientific accuracy.
- Develop therapeutic-area-specific evaluation criteria with business teams, reflecting domain-specific quality requirements per therapeutic area and application type.
- Define benchmarks for scientific validity, regulatory compliance, data quality, and operational reliability.
- Establish gold-standard validation datasets and automated evaluation pipelines.
- Lead structured vendor assessments producing written Evaluation Reports
- Challenge vendor claims with independent benchmarking; distinguish genuine capability from demonstration performance.
- Assess integration complexity, total cost of ownership, regulatory posture, and vendor lock-in risk.
- Serve as technical lead for the Evaluation & Standards Board, a cross-functional governance body for GenAI quality.
- Present evaluation findings and recommendations to the GenAI Portfolio Steering Committee.
- Define what “production-ready” means for GenAI in a regulated R&D environment and enforce that standard.
- Set evaluation gates for product development stages:
PoC, Limited Release, Scaled Product, and Product Ops.
- Partner with QMS/MLOps on the handoff from pre-adoption evaluation to production quality monitoring.
- Work with therapeutic area teams on domain-specific evaluation standards.
- Collaborate with Data Strategy & Products on data quality as an input to the evaluation rubric.
- Engage JJIT architecture teams on platform-layer evaluation and security assessments.
- Contribute to the weekly GenAI Outlook newsletter, specifically the evaluation implications of frontier AI developments.
- Build internal evaluation capability through training, documentation, and tooling for teams conducting…
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