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 |
|---|---|---|
| Manager, Insights Engineering & Innovation, Medical Affairs, Japan Manager leading insight analytics and AI-driven automation within Medical Affairs, focusing on GenAI, LLMs, NLP, and conversational AI. The role involves end-to-end lifecycle management of AI initiatives, from problem framing to deployment and monitoring, with a strong emphasis on operationalizing these capabilities in a regulated healthcare environment. Requires hands-on technical expertise in data engineering, ML/NLP, MLOps, and stakeholder management. | AgentPost-train | 7 |
| [Innovative Medicine] Project Lead, Regulatory Medical Writing, Japan Document Management Group, IB Translation Office/Publication Owner Office This role focuses on managing translation projects for clinical trial documents (Protocol, IB) and publications within Johnson & Johnson's Innovative Medicine division. A key responsibility is to transform the existing IB translation process by integrating AI translation technologies, managing CROs, and ensuring quality through proofreading. The role also involves leading cross-functional initiatives and team development. |
| — |
| 5 |
| [Innovative Medicine] R&D, Lead Payment Analyst, Site Engagement, Contract & Grants, Global Development This role is responsible for managing end-to-end investigator/site payment processes and calculations, purchase orders, and clinical trial payments within Johnson & Johnson's Innovative Medicine division. It involves acting as a liaison for issue resolution, understanding contract values, and utilizing various systems. The role also includes training study teams and new team members on payment processes and technology, with potential people management responsibilities. A key requirement is demonstrated AI literacy and the ability to apply AI tools to improve work efficiency and outcomes. | — | 1 |
| [MedTech] Specialist, CMO Office, Operational Excellence This role focuses on operational excellence within the MedTech CMO office at Johnson & Johnson. Key responsibilities include quality control of clinical and regulatory documents, managing QMS related activities like SOPs and training, overseeing J-EGC and Research Grants Office activities, managing the MIR process, and providing general business support. The role emphasizes adherence to procedures, collaboration, and process improvement. | — | 0 |
| [Innovative Medicine] Analyst, FF Testing, Quality Control Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant) The Analyst, FF Testing, Quality Control Group at Johnson & Johnson's Fuji Plant is responsible for performing various analytical tests (chemical, microbial, packaging material), method validation, and technical transfers to ensure compliance with regulatory requirements (JP, GMP/GCTP). The role involves training other analysts, writing and reviewing laboratory documents, managing deviations, maintaining knowledge of technology and GMP/GCTP standards, managing lab equipment lifecycle, and supporting product quality reviews. A Bachelor's degree in a science field and over 3 years of experience in the pharmaceutical industry are required, along with knowledge of GMP/GCTP, pharmaceutical regulations, analytical testing, and documentation. | — | 0 |
| [Innovative Medicine] R&D, Senior Local Trial Manager, x-TA Clinical Operation, GCO Japan This role is for a Senior Local Trial Manager in Innovative Medicine R&D at Johnson & Johnson, focusing on the operational management of clinical trials within Japan. The position involves overseeing trial activities from start-up to closeout, ensuring compliance with protocols, SOPs, GCP, and regulatory requirements. Responsibilities include leading local trial teams, managing budgets, coordinating with stakeholders, ensuring timely reporting of adverse events, and contributing to process improvements and training. | — | 0 |
| [Innovative Medicine] Staff, Quality System 2 Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant) Staff position in Quality Operations at Johnson & Johnson's Fuji Plant, focusing on quality systems and regulatory compliance within GMP/GCTP environments. Responsibilities include overseeing regulated substances, managing approvals, handling change notifications, operating recall processes, and executing new initiatives. Requires a degree in Pharmacy/Chemistry or equivalent experience, with a strong background in pharmaceutical quality and GMP. | — | 0 |
| [Innovative Medicine] R&D, Principal Statistical Programming Lead (Manager), Clinical & Statistical Programming Japan, Global Development The Principal Statistical Programming Lead will be responsible for the planning, oversight, and delivery of programming activities for clinical projects, compounds, or submissions. This role involves designing and developing programs and technical solutions for clinical research analysis and reporting, providing guidance to programming teams, and ensuring compliance with departmental processes and industry standards. The position also contributes to innovation and process improvement projects within the department. | — | 0 |
| [Innovative Medicine] R&D, Lead Local Trial Manager, Oncology Clinical Operation, GCO Japan Lead Local Trial Manager for Oncology Clinical Operations in Japan, responsible for the local management of clinical trials, ensuring data quality and compliance with protocols, SOPs, GCP, and regulatory requirements. This senior role involves coordinating local trial teams, managing budgets, and contributing to process improvement and training. | — | 0 |
| [Innovative Medicine] Staff, Quality Control Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant) Staff position in Quality Control Group at Johnson & Johnson's Innovative Medicine division in Japan. The role focuses on implementing, improving, and harmonizing laboratory quality systems in compliance with GMP/GCTP and J&J guidelines. Responsibilities include leading the transfer of analytical methods, overseeing QC activities for new product launches, ensuring system compliance for regulatory filings, managing stability programs, and supporting projects to improve efficiency and reduce costs. Requires a Bachelor's degree in a science field, 3+ years of pharmaceutical industry experience, and experience in GMP-compliant lab systems. | — | 0 |
| [Innovative Medicine] 生産物流本部 DELIVER JAPAN ディストリビューションセンター 東日本物流センター スタッフ This role is for a Distribution Center Staff position at Johnson & Johnson's Innovative Medicine division in Misato, Saitama, Japan. The primary responsibilities include managing the storage, receipt, and shipment of pharmaceutical products, handling inquiries, ensuring compliance with regulations like the Pharmaceutical and Medical Device Act, managing outsourced vendors, and participating in process improvement projects. The role requires strong communication, problem-solving, and compliance awareness, with experience in supply chain or the pharmaceutical/drug wholesale industry being essential. | — | 0 |
| [Medtech] Quality Operations Staff, Quality Control (Sukagawa) Quality Operations Staff, Quality Control role at Johnson & Johnson's MedTech division in Sukagawa, Japan. Responsibilities include managing incoming inspections and processes for active medical devices, overseeing external inspection vendors, coordinating with domestic and international teams, participating in new product introduction projects, and preparing for quality audits. Requires experience in manufacturing, QA/QC, GMP, ISO13485/ISO9001, and strong English communication skills. | — | 0 |
| ［MedTech］Data Strategy & Architecture Manager, Strategy & Commercial Excellence, Orthopedics Manager, Data Strategy & Architecture role at Johnson & Johnson (DePuy Synthes) focused on leading the development of data infrastructure in Japan, aligning with global digital strategy. Responsibilities include data governance, quality improvement, and designing data architecture across multiple systems (CRM, ERP, DWH). Collaborates with commercial, IT, and global teams to enable data-driven decision-making and business improvements. | — | 0 |
| [IT] Order to Cash (O2C) Product Manager [Shockwave] This role is for an Oracle Order to Cash (O2C) System Analyst at Johnson & Johnson in Tokyo. The primary responsibility is to design, implement, and support Oracle Cloud ERP functionalities related to order management, invoicing, and accounts receivable. The role requires extensive experience with Oracle ERP (EBS/Cloud) implementations, specifically in Order Management, Billing, Pricing, and Customer setups, as well as integrating with CRM applications like Salesforce and 3PL partners. The analyst will translate business needs into scalable solutions, manage O2C system issues, and collaborate with cross-functional teams. | — | 0 |
| Sr. Director, GDCL oUS Lead (Japan) Sr. Director, Global Deliver & Customer Logistics (GDCL) oUS Lead for Japan within DePuy Syntheshes Orthopedics. Responsible for overseeing and advancing GDCL strategy, ensuring compliant, efficient, and patient-focused supply chain operations, and leading transformation initiatives. Requires 12-15 years of experience in supply chain/logistics/operations leadership in a regulated industry, with strong knowledge of end-to-end supply chain processes. Fluent Japanese and English required. | — | 0 |
| [MedTech] Transport & Trade Operations Manager, Integrated Supply Chain, Deliver Japan The Transport & Trade Operations Manager is responsible for managing import and export operations, ensuring compliance with regulations, monitoring KPIs, managing freight costs, and collaborating with cross-functional stakeholders. This role requires experience in supply chain management, people management, and supplier management, with a strong emphasis on trade compliance and operational efficiency. | — | 0 |
| [Innovative Medicine] 生産物流本部 富士工場 オペレーションスタッフ This role is for an Operations Staff member in pharmaceutical manufacturing at Johnson & Johnson's Fuji plant in Japan. The primary responsibilities include leading inspection, manufacturing, and preservation operations according to correct procedures to ensure continuous production of quality products. The role involves managing production schedules, driving operational efficiency, safety, and quality control, and actively participating in factory improvement initiatives. Compliance with GMP and other regulations is critical. Experience with GMP/CGTP, Lean, or Six Sigma is preferred. | — | 0 |
| [Innovative Medicine] Specialist, Quality System 3 Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant) This role is a Specialist in Quality System within the Quality Operations Department at Johnson & Johnson's Fuji Plant. The primary responsibilities include managing GMP/GCTP activities such as risk assessments, investigations, CAPA, and change control. The role also involves supporting other team members, troubleshooting deviations, and leading or supporting improvement initiatives. A degree in Pharmacy, physics and chemistry, or biology is preferred, along with over 5 years of experience in quality control, quality assurance, or regulatory compliance in the pharmaceutical industry. Knowledge of GMP/GQP/QMS quality systems and business-level English proficiency are also desired. | — | 0 |
| [MedTech] Manager, CS Enablement, CKAM, Surgery/Cardio CS, Deliver, Integrated Supply Chain Manager for Customer Service Enablement within the MedTech sector, focusing on supply chain operations, process improvement, and team management. The role involves achieving KPIs, enhancing customer satisfaction, and collaborating with internal and external stakeholders to build an efficient and reliable supply chain. Key responsibilities include team leadership, developing growth strategies, coaching staff, managing resources, and driving automation initiatives. | — | 0 |
| [Innovative Medicine] 生産物流本部 富士工場 エンジニアリング部 エンジニア This role is for a Project Engineer in the Engineering Department at Johnson & Johnson's Fuji Plant in Shizuoka, Japan. The engineer will be responsible for the engineering, design, introduction, modification, and automation of manufacturing facilities and computer systems, as well as capital project execution. Key responsibilities include technical performance assurance of production equipment (validation), stable operation design for inspection machines, packaging lines, and computer systems, improvement of manufacturing facilities based on OEE, automation, and digital transformation, and vendor supervision. The role also requires supporting EHS policies and providing technical leadership. Compliance with GMP/GCTP, company policies, and regulations is mandatory. Desired experience includes working in pharmaceutical, cosmetic, or food industries, and business-level English proficiency. | — | 0 |
| [Innovative Medicine] Specialist, Quality System 2 Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant) This role is a Specialist in Quality System at Johnson & Johnson's Innovative Medicine division in Japan. The primary responsibilities involve ensuring compliance with GMP/GCTP regulations, managing quality systems, data integrity, deviation control, and change control. The role also involves acting as a point of contact with marketing authorization holders, supporting other team members, troubleshooting, and leading or supporting improvement initiatives. A degree in a scientific field and experience in pharmaceutical quality control/assurance/compliance are desirable. | — | 0 |
| [Innovative Medicine] 生産物流本部 富士工場 製造部 ビジネスユニット３ Warehouse This role is for a Warehouse position at Johnson & Johnson's Fuji plant in Japan. The primary responsibilities include executing warehouse operations according to company rules and SOPs, managing contractors, ensuring safe operation of equipment like forklifts and automated cranes, suggesting improvements for efficiency, conducting training to comply with GMP, reporting deviations and quality issues, performing 5S actions, coordinating with the support group for smooth delivery, executing sampling tasks accurately, and conducting safety training for drivers. The role also involves managing the handling, storage, and records for narcotic products in compliance with regulations. | — | 0 |
| [MedTech] Senior Supervisor, Repair Service, Operation Support Group, Japan Strategic Operations Center (Sukagawa) This role is a Senior Supervisor for Repair Service Operations Support in the MedTech division, focusing on back-office operations for a medical device repair center. Responsibilities include overseeing quality management (QMS), process improvement, cost reduction, supplier management, system implementation, and leading key initiatives. The role also involves people management, ensuring efficiency, quality, and compliance. Key activities include system maintenance, new product introduction support, measurement equipment management, overseas repair management, parts management, cross-departmental collaboration, budget support, KPI tracking, and reporting. It also involves leading global/APAC projects, expanding repair center functions, and driving improvement activities like automation, digitalization, cost reduction, and workplace environment improvement. Supplier management and team/people management are also core aspects. The role requires experience in leading technical projects or improvements in the medical device industry or similar sectors, with strong skills in quality management, business improvement (Lean, Kaizen, 5S), system operations (ERP, CRM, data analysis tools), data analysis, reporting, and business-level English. | — | 0 |
| [Quality] Quality Supervisor, Quality Assurance [AMO] Quality Supervisor for Johnson & Johnson's healthcare products (medical devices, pharmaceuticals) in Tokyo, Japan. Focuses on building, maintaining, and improving the quality management system, ensuring compliance with Japanese regulations (e.g., Pharmaceutical and Medical Device Act, GQP, QMS, GMP) and J&J's internal standards. Responsibilities include leading quality system processes, acting as a Subject Matter Expert, managing product quality and safety for market release, overseeing manufacturing quality control, conducting audits, managing documentation, supporting recalls, and preparing for regulatory inspections. Requires experience in QA/QC in the medical device/pharma industry, knowledge of relevant regulations, and strong leadership and communication skills. | — | 0 |
| [Innovative Medicine] R&D, Senior Local Trial Manager/Lead Local Trial Manager, Oncology Clinical Operation, GCO Japan This role is for a Lead Local Trial Manager in Oncology Clinical Operations at Johnson & Johnson in Japan. The position focuses on the local management of clinical trials, ensuring compliance with protocols, SOPs, GCP, and regulatory requirements. Responsibilities include coordinating local trial teams, managing study start-up to closeout, overseeing data quality, managing budgets, and mentoring junior staff. The role requires significant experience in clinical trial management or monitoring and may involve complex protocols across various phases and therapeutic areas. | — | 0 |
| [Innovative Medicine] 生産物流本部 富士工場 製造部 ビジネスユニット3 マネージャー （富士工場） This role is a Manufacturing Manager at Johnson & Johnson's Fuji Plant in Shizuoka, Japan. The manager will oversee production operations, ensure safety and quality, manage teams, drive process improvements (like OEE), and ensure compliance with GMP/CGTP regulations. The role requires collaboration with directors and factory heads, setting KPIs, conducting reviews, and supporting team development. Business-level English is required for teleconferences with international teams. | — | 0 |