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Johnson & Johnson

Makes prescription drugs and medical devices

Lead Engineer - Evidence Management

Enterprise ApplicationsUpdated on Nov 9
Full-time$102k - $175.9k

About the Job

Requirements

  • A bachelor's degree in Computer Science, Engineering, Information Systems, Data Science, AI/ML, or a related field.
  • At least 10 years of progressive experience in software engineering, application architecture, solution architecture, platform architecture, low-code platform architecture, data architecture, or enterprise technology delivery.
  • Hands-on experience engineering, architecting, and delivering solutions on the Appian platform.
  • Expertise in Appian solution design, including process modeling, interfaces, records, integrations, data models, rules, reports, role-based security, application lifecycle governance, and environment management.
  • Experience leading application engineering delivery in Agile or SAFe environments, including backlog shaping, technical design, code quality, release readiness, dependency management, and production support considerations.
  • Experience architecting or engineering AI-enabled enterprise solutions, including Generative AI and/or Machine Learning use cases.
  • Hands-on knowledge of Large Language Models, prompt engineering, semantic search, vector databases, Retrieval-Augmented Generation, model orchestration, AI observability, and responsible AI controls.
  • Experience designing secure, cloud-native, API-enabled, workflow-enabled, and data-centric platforms in complex enterprise environments.
  • Experience supporting regulated business functions such as Regulatory Affairs, Scientific Affairs, Quality, Clinical, Safety, R&D, or Life Sciences technology.
  • Working knowledge of GxP, SOX, privacy, cybersecurity, data integrity, regulated SDLC, validation, qualification, or computerized system assurance practices.
  • Ability to translate business operating models, regulatory processes, and evidence management needs into scalable technical architectures and delivery-ready engineering designs.

Responsibilities

  • Serve as Lead Engineer for evidence management capabilities covering regulatory and scientific workflow, case management, process automation, content and data flows, integrations, and user experience.
  • Define and guide application architecture for platforms supporting regulatory planning, submissions, evidence intake, evidence assessment, regulatory intelligence, workflow automation, post-approval activities, scientific evidence collaboration, and analytics.
  • Maintain primary focus on Regulatory Affairs delivery priorities while designing solutions that also support Scientific Affairs processes, evidence workflows, and cross-functional collaboration.
  • Identify high-value evidence management use cases, design scalable implementation patterns, and ensure responsible adoption in regulated environments.
  • Partner with Regulatory Affairs, Scientific Affairs, Quality, R&D, Supply Chain, Cybersecurity, Privacy, Data Governance, and IT delivery teams to translate business needs into compliant, maintainable technology solutions.
  • Act as lead technical advisor for Appian application decisions, integrations, data products, engineering practices, and AI-enabled capabilities across the evidence management ecosystem.
  • Own and maintain application architecture strategy and engineering roadmap for evidence management capabilities across Regulatory Affairs and Scientific Affairs.
  • Design scalable, interoperable, and compliant solutions across regulatory platforms, Appian applications, data flows, workflows, integrations, content repositories, and analytics capabilities.
  • Translate regulatory and scientific evidence processes into application designs, engineering patterns, data models, and delivery backlogs.
  • Drive design governance for new capabilities, major enhancements, technical debt remediation, platform modernization, and cross-system interoperability.
  • Ensure solution designs align with enterprise standards for cloud, cybersecurity, privacy, lifecycle management, supportability, and technical sustainability.
  • Lead engineering and application architecture for Appian-based regulatory workflow, evidence case management, process automation, integration, records, reporting, and user experience capabilities, and define Appian design standards.
  • Maintain understanding of Regulatory Affairs operating processes and technology needs across planning, submissions, regulatory intelligence, workflow orchestration, post-approval activities, content management, compliance, and analytics.
  • Ensure evidence management capabilities support traceability, auditability, role-based access, status visibility, decision history, and inspection-ready records where required.
  • Extend evidence management architecture and engineering patterns to support Scientific Affairs use cases such as evidence intake, evidence evaluation, collaboration workflows, knowledge search, scientific content traceability, and analytics.
  • Identify reusable process, data, content, workflow, and integration patterns across Scientific Affairs and Regulatory Affairs while respecting domain-specific controls.
  • Define the AI-enabled engineering roadmap for evidence management, including Generative AI, Machine Learning, natural language processing, semantic search, knowledge graphs, agentic workflows, and intelligent automation where appropriate.
  • Guide proof-of-concepts, pilots, and scaled AI implementations with business value, security, usability, and compliance controls.
  • Establish patterns for monitoring, hallucination risk mitigation, source traceability, human-in-the-loop review, prompt and version governance, and model performance evaluation.
  • Define data architecture principles for evidence metadata, Appian data models, regulatory master data, scientific evidence content, operational data, unstructured content, and analytics-ready data products.
  • Establish engineering standards for APIs, event-driven integration, workflow orchestration, data lineage, data quality, access control, and platform interoperability.
  • Ensure engineering and architecture decisions support GxP, SOX, privacy, cybersecurity, auditability, data integrity, validation or qualification expectations, and regulated SDLC or computerized system assurance practices.
  • Partner with Quality, Security, Privacy, Regulatory Affairs, Scientific Affairs, and Data Governance stakeholders to assess technology, Appian-specific, evidence-management-specific, and AI-specific risks.

Desired Qualifications

  • Appian certification or equivalent demonstrated enterprise Appian engineering and architecture experience.
  • Experience with Regulatory Affairs platforms, RIM solutions, submission management, regulatory intelligence, regulatory analytics, content management, knowledge management systems, or evidence management platforms.
  • Experience supporting Scientific Affairs, Medical Affairs, evidence generation, scientific content workflows, or knowledge search capabilities.
  • Experience with Microsoft Azure AI services, Azure OpenAI, Copilot extensibility, AI Foundry, agent frameworks, or equivalent enterprise AI platforms.
  • Experience applying AI in regulated environments, including human-in-the-loop workflows, validation strategy, model monitoring, data governance, and risk-based controls.
  • Architecture, engineering, or Agile certifications such as TOGAF, Azure Solutions Architect, Appian certification, SAFe Architect, SAFe Agilist, or equivalent.
  • Experience leading vendor technology assessments, Appian solution reviews, AI platform evaluations, proof-of-concepts, and enterprise-scale implementation planning.
  • Agile Methodology, Agile Product Development, Agile Software Development, Agile Workforce, Analytics Dashboards, Change Control Management, Human-Computer Interaction, Organizational Design, Program Management, Risk Management, Software Development Management, or Technical Writing.

About the Company

Johnson & Johnson

Makes prescription drugs and medical devices

Johnson & Johnson develops prescription medicines and makes medical devices for hospitals, and unlike most big drugmakers, it runs both businesses under one roof. In 2015, its Darzalex became the first antibody drug approved for multiple myeloma, a blood cancer. Its medicines treat cancer, immune diseases such as psoriasis, and mental illnesses such as depression, and patented drugs bring in most of its sales. Its MedTech unit makes heart pumps, catheters that treat irregular heartbeats, surgical sutures, and Acuvue contact lenses. It was founded in 1886 to make sterile surgical dressings, is based in New Brunswick, New Jersey, and spun off its consumer brands, such as Tylenol and Band-Aid, as Kenvue in 2023.

Company size
10,001+
Company stage
IPO
Headquarters
New Brunswick, NJ
Founded
1886

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