Johnson & Johnson currently has 73 active AI-related job listings. The majority of these roles, specifically 44%, are in the agents stage. Engineering is the most frequent function for these hires, followed by Product. The company is primarily hiring in the United States. Frequent tech tags include agent_orchestration and model_serving, suggesting a focus on AI system deployment and management. In the last 30 days, Johnson & Johnson posted 104 new AI roles, representing a significant increase of 420% compared to the previous 30-day period.
Currently tracking 49 active AI roles, down 53% versus the prior 4 weeks. Primary focus: Agent · Engineering. Salary range $77k–$283k (avg $144k).
Johnson & Johnson currently has 62 active AI-related roles in our index. The most common open titles are: Principal Scientist, Data Science - DDSAI - Therapeutics Development Supply (4), Data Scientist and Application Developer (2), Lead-Data Automation and Excellence (2), Postdoctoral Data Analytics Computational Sciences (2), Senior Program Manager, R&D (2). Most positions are in Engineering and Product.
Johnson & Johnson's active AI hiring is concentrated in: agents (40%), application (19%), data (18%). These categories follow a seven-stage AI lifecycle: data, pre-training, post-training, serving infrastructure, agents, evaluation, and application.
Johnson & Johnson is hiring AI talent in: United States (38 roles), Spain (7 roles), Belgium (5 roles), Japan (4 roles).
Job postings at Johnson & Johnson most frequently reference: agent orchestration, model serving, llm observability, fine tuning, rag.
In the past 30 days, Johnson & Johnson has posted 69 new AI-related roles. That is a -37% change versus the prior 30 days (109 → 69).
| Title | Stage | AI score |
|---|---|---|
| Dir Tech Prod Mgmt Director of AI Fabric and Data Platforms responsible for leading the enterprise AI Services and Data Foundation capability, ensuring scalable, secure, and high-impact delivery of end-to-end AI services. Owns the full lifecycle of AI services and leads the evolution of a unified 'AI Agent Factory' platform to produce reusable AI agents that automate business workflows. Also responsible for Data Platforms strategy and execution. | AgentServe | 8 |
| Post Doctoral Researcher, Evaluation & Standards in Clinical Operations Postdoctoral researcher to develop evaluation frameworks, rubrics, and quality systems for generative AI agents used in clinical operations and global development workflows. The role involves defining quality dimensions, designing human evaluation protocols, building benchmark datasets, and partnering with AI engineering teams in a regulated pharmaceutical environment. |
| Eval GateAgent |
| 8 |
| Principal Scientist, Data Science - DDSAI - Therapeutics Development Supply Seeking a Principal Data Scientist to design, build, validate, and deliver applied AI/ML and statistical modeling solutions for Drug Product Development & Supply (DPDS) within Johnson & Johnson Innovative Medicine. The role involves hands-on model development, translating scientific questions into modeling problems, and ensuring model robustness and actionability. It also requires applying software engineering best practices, collaborating with cross-functional teams, and providing technical guidance. Experience in pharmaceutical development or a related quantitative field is preferred. | Post-train | 7 |
| Postdoctoral Scholar, AI/ML for drug metabolite prediction and LC-MS analytical chemistry This role focuses on developing and evaluating AI/ML models for drug metabolite prediction, pharmacokinetics, and molecular properties within a healthcare/drug discovery context. It involves fundamental research using internal datasets, developing explainable AI tools with uncertainty estimation and active learning, and publishing findings. The role is primarily research-oriented, building and evaluating deep learning methods for analytical instrumentation and drug discovery processes. | Post-train | 7 |
| Postdoc on cofolding models for In-Silico Drug Discovery Postdoctoral researcher focused on developing and fine-tuning co-folding models for in-silico drug discovery, involving dataset curation, model evaluation, and integration into discovery workflows within a healthcare/biotech domain. | Post-train | 7 |
| Director, Product Information Management - VCM Director, Product Information Management (PIM) role focused on transforming product information and execution workflows across Value Chain Management (VCM) by establishing a product-centric digital backbone. This role involves leading a team, redesigning workflows, defining strategy, driving adoption, and ensuring data trust. It also includes ownership of the IMSC Quickbase platform and operating a center of excellence. The position requires significant experience in business process transformation, workflow digitization, and data management within a supply chain or related field, with a preference for experience in regulated environments. | — | 0 |
| Director HEMA EMEA The Director, HEMA Surgery EMEA is responsible for defining and executing Health Economics, Market Access, and Reimbursement (HEMA) strategies for the Surgery portfolio across the EMEA region. This role ensures alignment with business priorities to accelerate patient access and drive sustainable growth by developing robust health economic arguments and tools that support value demonstration, funding, and procedural adoption. Key responsibilities include leading health economics research (RWE, budget impact models), developing economic evidence and value narratives, securing reimbursement, and monitoring healthcare policy trends. The role also involves leading a team and managing budgets. | — | 0 |
| Transcend Global PMO Operations Manager Johnson & Johnson is seeking a PMO Operations Manager for their Transcend global business transformation program. This program aims to modernize foundational transactional processes and consolidate seven ERP systems into one S/4 HANA platform for the Innovative Medicine business. The role involves supporting day-to-day PMO operations, including planning, governance coordination, risk management, reporting, and decision-support processes to ensure successful execution and delivery excellence. | — | 0 |
| Transcend Global PMO Operations Manager Johnson & Johnson is seeking a PMO Operations Manager for the Transcend global business transformation program. This role will support delivery excellence and global PMO consolidations, focusing on modernizing foundational transactional processes and harmonizing them into one S/4 HANA ERP platform for the Innovative Medicine business. Responsibilities include leading PMO operations, governance, planning, risk management, reporting, and cross-functional coordination to ensure successful program execution. | — | 0 |
| Medical Technologist Cryopreservation Medical Technologist specializing in cryopreservation for CAR-T cell therapy production. Responsibilities include formulation and cryopreservation of white blood cells, ensuring high quality, and adhering to regulations. Requires a bachelor's degree in a relevant field or equivalent experience in a regulated environment, with a focus on detail and quality. Experience in pharmaceutical, food, chemical, or biotech sectors is valued. | — | 0 |
| Transcend PMO Operations Manager Johnson & Johnson is seeking a PMO Operations Manager for their Transcend program, a global business transformation initiative to modernize and standardize transactional processes by consolidating seven ERP systems into one S/4 HANA platform. The role involves managing day-to-day PMO operations, including planning, governance, risk management, reporting, and decision support, to ensure successful program execution at scale. The manager will lead PMO resources, coordinate cross-functional teams, and ensure alignment with compliance and quality standards. | — | 0 |
| Transcend PMO Senior Operations Manager Johnson & Johnson is seeking a PMO Senior Operations Manager to support a global business transformation program focused on modernizing foundational transactional processes and consolidating seven ERP systems into one S/4 HANA platform for the Innovative Medicine business. The role involves leading PMO operations, governance, planning, risk management, reporting, and resource leadership to ensure delivery excellence. | — | 0 |
| Experienced Scientist (Neurodegeneration, Neuroinflammation, and Translational Biology) Experienced Scientist role in neurodegeneration and neuroinflammation research, focusing on Alzheimer's disease. The role involves designing and executing complex in vitro (iPSC-derived systems) and in vivo experiments, applying molecular and cellular techniques, and ensuring high-quality data generation. Requires a Master's degree with 6+ years of experience or a PhD, extensive hands-on experience with iPSC systems, and a proven track record in the field. | — | 0 |
| Senior Clinical Research Associate (Site Manager) Senior Clinical Research Associate (Site Manager) at Johnson & Johnson, responsible for overseeing clinical trial sites, ensuring compliance with protocols, SOPs, GCP, and regulations from study start-up to closure. The role involves site initiation, monitoring, management, and close-out, implementing risk-based monitoring, and collaborating with trial teams on recruitment and issue resolution. Requires a BA/BS in Life Sciences or related field, minimum 3 years of clinical trial monitoring experience, strong understanding of GCP and regulations, and fluency in Dutch and English (or Dutch, English, and French in Belgium). | — | 0 |
| Director HTA Statistics & RWE Methods The Director HTA Statistics & RWE Methods role at Johnson & Johnson provides strategic and technical leadership for data generation initiatives in innovative medicines. Responsibilities include dataset feasibility, protocol development, study design, and dissemination of results for indirect treatment comparisons, post hoc trial analyses, and real-world evidence (RWE). The role supports market access and launch strategies by leading the design of advanced study designs and statistical analyses aligned with Payer/HTA expectations. It also involves contributing to capability building, including training on Payer/HTA requirements and new methodologies, and development of coding libraries and AI/ML advanced analytics scaling and platforms. | — | 0 |
| Experienced Scientist (temp role) Scientist role at Johnson & Johnson focused on developing dissolution and in vitro release methods for new medications. The role involves hands-on lab work, predictive modeling, data science, and contributing to automation and mechanistic understanding of dissolution. It requires a PhD or Master's degree with relevant experience and strong analytical and communication skills. | — | 0 |
| Senior Manager, Global Customer Solutions North Senior Manager, Global Customer Solutions North for Johnson & Johnson MedTech, responsible for leading end-to-end customer service operations, driving continuous improvement, and managing a multi-tiered team. The role involves implementing AI solutions into Customer Service and adapting global tools to local market requirements. | — | 0 |
| Supervisor CAR-T Cryopreservation (Shifts 8:00 - 16:00 / 14:00 - 22:00) Supervisor for CAR-T Cryopreservation Center overseeing daily operations, planning, and team management to ensure productivity and GTP compliance. The role involves leading a team of lab technicians, managing performance, ensuring operational efficiency, and supporting investigations and audits within a regulated healthcare environment. | — | 0 |
| Manager, Transcend R&D BPO Plan and Source Johnson & Johnson is seeking a Manager, Transcend R&D BPO Plan and Source to define and evolve future state, value-driven E2E processes within R&D for their global business transformation program. This role involves standardizing supply chain processes on SAP S/4 Hana, developing CMO integration strategies, and ensuring alignment with global templates and regulatory expectations. The position requires extensive experience in R&D or supply chain leadership, SAP S/4HANA, and global BPO roles, with a focus on driving business value and continuous improvement in a regulated environment. | — | 0 |
| QA Associate Commercial Johnson & Johnson is seeking a QA Associate Commercial in Geel, Belgium, to oversee the quality and timely release of commercial Active Pharmaceutical Ingredients (APIs). This role involves ensuring compliance with regulations, supporting investigations of non-conformances, and collaborating with stakeholders to maintain a reliable supply chain for pharmaceutical products. | — | 0 |
| Staff Facilities Engineer - Coordinator Staff Facilities Engineer - Coordinator role at Johnson & Johnson in Ghent, Belgium, focusing on managing daily operations of two facilities, supervising contractors, and overseeing preventive, corrective, and predictive maintenance. The role requires strong technical expertise in electrical, mechanical, and automation, adherence to quality management systems (QMS), EHS requirements, and proficiency in CMMS for asset management and reporting. Experience in GxP and maintenance reliability principles is essential. | — | 0 |
| Senior CSQ Associate This role is for a Senior CSQ Associate in the Clinical Supply Quality team at Johnson & Johnson. The primary focus is on reviewing and approving complaint investigations, ensuring scientific soundness and compliance. The role also involves contributing to complex investigations, process improvements, and acting as a Quality Lead for investigations related to Clinical Supply Planning and Logistics. While the role mentions an understanding of AI concepts and frameworks for efficiency, it is not core to the job function. | — | 0 |
| Shift Support Specialist This role supports plant operations by overseeing contractor activities, managing work permits, troubleshooting issues in a regulated environment, and coordinating technical changes. It involves ensuring safety, quality, and operational efficiency on the production floor. | — | 0 |
| Manager Clinical Trial Payments Manager for Clinical Trial Payments at Johnson & Johnson, responsible for overseeing regional site payments, issue resolution, and training related to clinical trial management systems (mCTMS) and payment processes. The role involves process ownership, driving continuous improvement, managing a global team, and ensuring compliance with healthcare regulations. | — | 0 |
| MSAT Synthetics DP External site Principal Scientist Johnson & Johnson is seeking a Principal Scientist for their MSAT Synthetics Drug Product External Site team. This role involves providing technical oversight to external manufacturing sites, including due diligence, auditing, and onboarding. Responsibilities include technical/risk assessment for New Product Introduction (NPI), technical transfers, and Product Life Cycle (LCM) management, as well as deploying new technologies and performing statistical analysis. The scientist will act as a primary technical contact for external manufacturers and ensure compliance with quality and regulatory standards. | — | 0 |
| MSAT Sr Process Engineer W&L Johnson & Johnson is seeking an MSAT Sr. Process Engineer W&L to focus on weighing and logistics, material/packaging/consumables qualification, process validation/verification, cost and process improvements, and new technology deployment (PAT, digitalization). The role involves managing qualifications, supporting operations, monitoring process performance, leading investigations, and contributing to standardization and innovation in pharmaceutical manufacturing. | — | 0 |
| Site Quality Head, Geel This role is for a Site Quality Head at Johnson & Johnson in Geel, Belgium. The position involves leading and managing all quality-related programs and activities for manufacturing operations, ensuring compliance with cGMP, regulatory policies, and guidelines. The Head will oversee Quality Control, Quality Assurance, Quality Systems, Compliance, and Product Release, and will be a key member of the site leadership team, partnering with global quality teams and regulatory bodies. | — | 0 |
| Computer Systems Validation - Lab Instruments Computer Systems Validation role focused on lab instruments within a pharmaceutical Quality Engineering team, ensuring compliance with regulations and implementing new technologies. This role is not directly involved in AI/ML model development but ensures the systems used in a regulated healthcare environment are validated and compliant. | — | 0 |
| Mobile Equipment Operator Mobile Equipment Operator responsible for cleaning production parts, materials, and tools in a healthcare manufacturing environment, ensuring contamination-free deployment and adhering to strict GMP, safety, and environmental regulations. Requires manual and specialized cleaning, basic technical knowledge, and physical capability. | — | 0 |
| Postdoctoral Researcher - Translational PBPK/PD Modeling Postdoctoral Researcher to join the Translational PBPK/PD modeling group, focusing on mechanistic modeling at the interface of pharmacology, biology, and quantitative data science for oncology drug development. The role involves developing and applying innovative mechanistic translational modeling strategies to integrate various data streams and improve human dose prediction for next-generation solid tumor therapies. | — | 0 |
| Postdoctoral Researcher– Translational PK/PD & Investigative Toxicology This postdoctoral researcher position focuses on developing and utilizing organotypic translational in vitro tumor models, including patient-derived organoids, to support the characterization of next-generation solid tumor therapies. The role involves employing advanced in vitro models with spatial biology approaches and developing pharmacodynamic (PD) and pharmacology endpoints to understand anti-tumor responses and predict human dose. The position emphasizes contributing to New Approach Methodologies (NAMs) and requires hands-on experience with organoids, tumoroids, bio-printed platforms, and co-culture models with immune cells. | — | 0 |
| Senior Engineer Computer System Validation This role focuses on Computer System Validation (CSV) and Data Integrity within a drug product manufacturing environment. The Senior Engineer will provide expertise on validation strategy, regulatory compliance, and data integrity, ensuring systems are fit-for-purpose, especially in evolving environments involving automation, AI, and digitalization. The role involves working with cross-functional teams, defending validation strategies during audits, and owning/improving CSV processes. While AI is mentioned as an evolving environment, the core function is validation and compliance, not direct AI/ML development. | — | 0 |
| Demand Planning Transformation Sr Man Johnson & Johnson is seeking a Demand Planning Transformation Lead to develop and deploy a global Plan System transformation program for Demand Planning across all MedTech Business Units and Regions. This role involves shaping the vision and strategy, managing complex interdependencies with other strategic programs, and ensuring the successful delivery of the program. The Lead will also transform and standardize underlying Plan technologies and ensure their integration. The position reports to the MedTech Plan Product Owner within the J&J MedTech Supply Chain Digital organization. | — | 0 |
| Manager, Transcend R&D Logistics and Global Trade Systems Manager for Transcend R&D BPO Logistics and Global Trade Systems at Johnson & Johnson, focusing on modernizing supply chain processes and standardizing them onto SAP S4 Hana. The role involves owning end-to-end process vision, translating business strategy into a capability roadmap, and ensuring alignment with global template and clean core principles. | — | 0 |
| Director, Category management and Procurement Excellence (m/f/d) Director, Category Management and Procurement Excellence for Johnson & Johnson MedTech's Heart Recovery business unit. This role will oversee external spending for direct materials, including precision materials, external manufacturing, and electronics. Responsibilities include driving end-to-end spend performance, supply security, risk management, sourcing strategies, innovation, and procurement excellence. The role also involves people management of a team of 15+, including category management leads and a Data Analytics and Governance lead. | — | 0 |
| Manager Quality Assurance Manager of Quality Assurance for commercial APIs at Johnson & Johnson, responsible for ensuring compliance with regulations, leading a team, and overseeing API production plant quality. The role involves managing deviations, CAPAs, change controls, and acting as a liaison during health authority inspections and audits. Requires a Master's degree in a scientific field and at least 5 years of experience in supply chain or QA, with proven experience in commercial product release. | — | 0 |
| Postdoc Product development Postdoctoral Scholar role focused on developing advanced in vitro characterization methods for lipid-based formulations to improve drug delivery of beyond rule of five (bRo5) drug candidates. The role involves building and exploring experimental toolboxes, designing formulation strategies, supporting in vivo translation, and communicating scientific outcomes. | — | 0 |
| Associate Director, Global Market Access Analytics & RWE This role focuses on designing and executing market access analytics and Real World Evidence (RWE) studies, specifically indirect treatment comparisons, to support Health Technology Assessment (HTA) and payer submissions within the pharmaceutical industry. It involves applying advanced statistical methods and programming to diverse data sources. | — | 0 |
| QMS Deviation Specialist Johnson & Johnson is seeking a QMS Deviation Specialist in Beerse, Belgium. This role is responsible for the Non-Conformance/Corrective and Preventive Action (NC/CAPA) process, acting as the Business Process Owner. The specialist will collaborate with global teams, provide training, monitor KPIs, identify compliance needs through data analysis, and ensure inspection readiness. The role requires strong communication skills in English and Dutch, experience in a pharmaceutical quality role, and knowledge of GMP and Quality Management Systems. While the role is primarily focused on quality systems, it also mentions an understanding of AI concepts and prompt generation for efficiency. | — | 0 |
| Technical Product Owner - Logistics WM Technical Product Owner for Logistics Warehouse Management within the Pharm Transcend program at Johnson & Johnson. This role focuses on designing and implementing SAP S/4 capabilities and data for logistics and warehouse management, with integration to 3PLs. The goal is to modernize foundational transactional processes and standardize them into a single ERP platform. | — | 0 |
| Health Economics Modeling Associate Director The Associate Director Health Economics - Modeling will lead the development, refinement, and adaptation of economic models including cost-effectiveness and budget impact models. This role involves hands-on development, management, and quality assurance of models, utilizing data from clinical trials, quality of life studies, costing studies, literature reviews, and retrospective analyses. The position requires advanced skills in Excel, Visual Basic, and R, and an understanding of reimbursement requirements. | — | 0 |
| Medical Affairs Lead (m/f/d) - Surgery MSM Johnson & Johnson is seeking a Medical Affairs Lead for their Surgery MSM portfolio. This role is responsible for shaping and executing the medical and clinical strategy, providing scientific and clinical leadership, and collaborating with internal and external stakeholders to support decision-making and evidence-based value propositions. The role requires an MD or equivalent medical degree and 5-10 years of experience in clinical practice, research, or medical affairs. | — | 0 |
| Post Doc – Solid-State NMR & Peptide–Formulation (Mechanistic Insights) Postdoctoral scientist role focused on understanding molecular interactions for oral peptide delivery using solid-state NMR, complementary spectroscopy, and computational modeling. The role aims to generate mechanistic insights to guide the design of new functional excipients. | — | 0 |
| Senior Scientist, Reference Standard Process Owner Senior Scientist, Reference Standard Process Owner at Johnson & Johnson, responsible for the overall reference standard certification and stock management for R&D and commercial compounds. This role involves coaching other owners, ensuring compliance with GMP regulations, managing stock, leading process improvements, and acting as a subject matter expert in a pharmaceutical R&D setting. | — | 0 |
| Automation Technology Product Owner - Synthetics Development Product Owner for Lab Automation Suite focused on accelerating Synthetics Development. The role involves defining product vision, roadmaps, and features, translating user needs into requirements, managing the product backlog, and collaborating with engineering and automation teams to improve efficiency and data quality in a scientific and regulated environment. | — | 0 |
| Crystallographer, Experienced Scientist R&D This role focuses on crystallography and solid-state chemistry to characterize and control polymorphism of active pharmaceutical ingredients (APIs) for drug development. It involves applying expertise in X-ray, electron, or neutron diffraction techniques for structure determination and analysis, collaborating with cross-functional teams, and ensuring compliance with laboratory standards. The role requires a PhD in a related field and experience in solid-state materials science. | — | 0 |
| Sr Mgr Project Engineering This role is for a Sr. Manager of Project Engineering at Johnson & Johnson, focusing on leading engineering and design activities for large capital infrastructure projects. Responsibilities include defining project requirements, preparing RFPs, leading design phases, collaborating with suppliers and internal teams, and ensuring compliance with J&J standards and regulatory requirements. The role requires a Bachelor's degree in Engineering and 8 years of experience in capital facility projects. | — | 0 |
| Sr Mgr Project Engineering Johnson & Johnson is seeking a Sr Manager Project Engineering to lead engineering and design activities for large capital infrastructure projects. This role involves defining project requirements, managing RFPs, coordinating design development, and ensuring compliance with J&J standards and regulatory requirements. The manager will also contribute to regional operational strategies and talent development. | — | 0 |
| Senior Compliance Lead This role is for a Senior Compliance Lead at Johnson & Johnson, focusing on managing internal audit programs and external GMP inspections for the Geel site. The position requires expertise in pharmaceutical regulatory compliance, coordinating compliance personnel, and ensuring site inspection readiness. It involves identifying regulatory changes, providing compliance subject matter expertise, and facilitating remediation of compliance risks. | — | 0 |
| Senior Manager Clinical Operations Johnson & Johnson is seeking a Senior Clinical Research Manager to manage a team of Local Trial Managers, Site Managers, and Clinical Trial Assistants. The role focuses on trial delivery in oncology, site engagement, staff development, training, onboarding, and resource management. Responsibilities include overseeing trial execution from feasibility to close-out, ensuring quality, timelines, and compliance with SOPs, HCC, and local regulations. The role also involves contributing to country strategy, optimizing ways of working, driving innovation, and continuous improvement. | — | 0 |