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 50% 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 67 new AI-related roles. That is a -39% change versus the prior 30 days (109 → 67).
| Title | Stage | AI score |
|---|---|---|
| New Product Introduction Supply Analyst-Orthopedics Johnson & Johnson's DePuy Synthes is seeking a New Product Introduction Supply Analyst to manage portfolio management, intake, and orchestration of LCM and NPI projects for the Shoulders portfolio. This role ensures operational readiness, supply continuity, and cross-functional alignment for new product launches and product changes, translating strategic decisions into executable supply chain plans. | — | 0 |
| New Product Introduction Supply Analyst-Orthopedics This role is for a New Product Introduction Supply Analyst in the Orthopedics sector of Johnson & Johnson. The analyst will be responsible for portfolio management, intake, and orchestration of LCM and NPI projects, ensuring operational readiness, supply continuity, and cross-functional alignment for new product launches. They will develop supply chain strategies, manage inventory and capacity, partner with various departments, and track key performance indicators related to service, inventory, and launch readiness. | — |
| 0 |
| Patient Support Supervisor, CAR-T - Horsham, PA Supervise and lead a team of patient support specialists for a CAR-T therapy, ensuring patients receive logistical and reimbursement support throughout their treatment journey. Responsibilities include operational oversight, quality assurance, process improvement, and team coaching. | — | 0 |
| Director, Medical Affairs, Can & LATAM Johnson & Johnson is seeking a Director, Medical Affairs for Brazil, Chile, Colombia, United States, and Canada to provide strategic and operational leadership for Medical Affairs across the Americas region. This role ensures the safe, compliant, and effective generation and communication of scientific and clinical evidence supporting DePuy Synthes orthopedic products. Responsibilities include leading regional medical affairs strategy, providing scientific and clinical leadership, overseeing evidence generation, building relationships with healthcare professionals, and ensuring compliance with regulations. The role requires an advanced degree in a life sciences discipline, 10-12 years of experience in Medical Affairs within the pharmaceutical or medical device industry, and demonstrated people leadership experience. | — | 0 |
| Director, Medical Affairs, Can & LATAM Director, Medical Affairs for Brazil, Chile, Colombia, United States and Canada, providing operational leadership for Medical Affairs across the Americas region, ensuring the safe, compliant, and effective generation and communication of scientific and clinical evidence supporting DePuy Synthes orthopedic products. This role plays a critical leadership position in shaping medical strategy, advancing evidence generation, and strengthening partnerships with healthcare professionals, scientific societies, and internal stakeholders. | — | 0 |
| National Field Director, Thought Leader Liaison, Dermatology - East National Field Director for Thought Leader Liaison in Dermatology, East region, at Johnson & Johnson. This senior role focuses on leading a team of TLLs, building medical education strategy, managing speaker bureaus, and engaging with Key Opinion Leaders (KOLs) in the dermatology field. The position requires strong people management, KOL relationship development, and ensuring adherence to regulatory guidelines for medical education. | — | 0 |
| Sr Engineer Quality Engineering This role is for a Sr. Engineer Quality Engineering in the medical device industry, focusing on ensuring new and existing medical devices meet their intended use. Responsibilities include providing quality and technical leadership, establishing and meeting Critical to Quality (CTQ) attributes, leading design control strategy, collaborating with functional partners, and managing risk management activities. The role requires a Bachelor's degree in Engineering or a related technical field, 4 years of experience in a regulated industry, and practical understanding of QSR/ISO medical device regulations. | — | 0 |
| Spine, Sports & CMF Senior Manager of Strategy & Execution, Supply Chain This role is a Senior Manager of Strategy & Execution within the Supply Chain for Johnson & Johnson's Spine, Sports & CMF business. The position focuses on driving execution, coordination, and follow-through of critical priorities, translating strategic ideas into action, and maintaining organizational momentum. Responsibilities include shaping business strategies, managing a portfolio of supply chain projects, developing business cases, executing strategic programs, overseeing cost reduction initiatives, leading financial and strategic planning cycles, managing portfolio metrics and governance, and developing executive-level summaries. | — | 0 |
| Sr. Analyst, Trade Operations This role is for a Sr. Analyst, Trade Operations at Johnson & Johnson, focusing on ensuring compliant and timely movement of products by providing advice and training on trade compliance processes, managing product classifications, responding to inquiries, and identifying trade compliance opportunities. The role involves collaboration with business partners and operating companies to review assessments, develop training, and implement compliance improvement plans. | — | 0 |
| Manager External Manufacturing Category Johnson & Johnson is seeking a Manager External Manufacturing Category to support end-to-end procurement strategy, delivering cost efficiency, quality, innovation, and sustainability outcomes. The role involves partnering with Supply Chain, Quality, R&D, Legal, and Finance to shape sourcing strategies, manage supplier relationships, negotiate commercial agreements, and drive cost reductions. The position requires a minimum of 6 years of relevant experience, strong analytical, negotiation, project management, and communication skills, with familiarity with digital and AI tools. | — | 0 |
| Associate Director, Global Compound Market Access, Oncology This role focuses on developing and implementing market access strategies for oncology treatments, specifically Bladder Cancer. It involves contributing market access expertise to global brand strategy, clinical development, and integrated evidence generation plans. The Associate Director will support the creation of value propositions, ensure optimal reimbursement in diverse regions, monitor market dynamics, and collaborate with various internal teams (Health Economics, Patient Reported Outcomes, Access Policy, Pricing, Real-World Evidence & Analytics) and external stakeholders. | — | 0 |
| Regulatory Affairs Specialist I – Spine This role provides regulatory guidance to product development teams, executes submissions for new and existing products, ensures conformance with regulations, and supports product launches and international registrations within the healthcare industry. | — | 0 |
| Finishing Tech This role supports manufacturing processes by applying basic electro-polishing and metal finishing theories to diagnose and correct problems. It involves operating and maintaining facilities equipment, repairing the physical structure of the establishment, and managing facility-related projects including remodeling, equipment installation, and compliance. The role also includes performing mechanical and preventive maintenance, troubleshooting electrical systems, coordinating inspections, and training lower-level technicians. | — | 0 |
| Associate Director, TLL Field Leader, CAPLYTA Associate Director, TLL Field Leader for CAPLYTA, responsible for leading a team of Thought Leader Liaisons to execute KOL engagement and peer-to-peer education strategies in the neuroscience therapeutic area. This role focuses on translating national strategy into regional execution, ensuring compliance, and gathering field insights. | — | 0 |
| Engineer Entry to developing individual contributor in a scientific/technology field focused on Supply Chain Engineering within Manufacturing Engineering at Johnson & Johnson's Vision division. The role involves planning and executing change control projects, qualifying new equipment, implementing project management methodologies, participating in technical design reviews, and collaborating cross-functionally to meet business objectives. Requires a University/Bachelors Degree in Engineering and 0-2 years of experience. | — | 0 |
| Associate Engineer Associate Engineer role in Supply Chain Manufacturing Engineering at Johnson & Johnson Vision, focusing on project coordination, development, and implementation for improved performance and efficiencies. The role involves managing change control projects, qualifying new equipment, and collaborating with cross-functional teams in a regulated environment. | — | 0 |
| Staff Engineer Staff Engineer in Supply Chain Engineering at Johnson & Johnson Vision, focusing on manufacturing engineering. Responsibilities include managing complex change control projects, qualifying new equipment, implementing project management methodologies, participating in design reviews, and resolving corrective/preventative actions. Requires a Bachelor's degree in Engineering and 4-6 years of experience. Preferred experience in regulated environments and vendor management. | — | 0 |
| Sr Human Factors Engineer The Senior Human Factors Engineer will support the development and execution of human factors and usability strategies for the OTTAVA™ Robotic Surgical System. This role involves collaborating with cross-functional teams, conducting usability testing, and ensuring user-centered design throughout the product lifecycle, with a focus on medical devices. | — | 0 |
| Associate Engineer Associate Engineer role in Supply Chain Manufacturing Engineering at Johnson & Johnson Vision, focusing on developing and implementing manufacturing engineering principles and project plans. Requires a Bachelor's degree in Engineering and 0-2 years of experience, with preferred experience in regulated environments and vendor management. | — | 0 |
| Staff Engineer Staff Engineer in Supply Chain Engineering at Johnson & Johnson Vision, focusing on manufacturing engineering. The role involves identifying, planning, and executing complex change control projects, qualifying new equipment, implementing project management methodologies, and participating in technical design reviews. Key responsibilities include analyzing production data, applying statistical methods, building KPI dashboards, using data tools for insights, pulling data from manufacturing systems, ensuring data integrity, identifying process improvement opportunities, supporting continuous improvement initiatives, performing root cause analysis, and developing data-driven recommendations. The role requires a Bachelor's degree in Engineering and 4-6 years of experience, with preferred experience in regulated environments (ISO, FDA) and manufacturing operations. | — | 0 |
| Engineering Lead - Device Assembly and Packaging Engineering Lead for Device Assembly and Packaging within the Global Engineering & Technology (GET) team at Johnson & Johnson's Innovative Medicine Supply Chain. The role involves leading a team of project engineers and qualification professionals, managing CAPEX portfolios, driving engineering standards, and supporting business case development for pharmaceutical manufacturing. | — | 0 |
| Associate Director, Global MAA & RWE Associate Director, Market Access Analytics and Real World Evidence (MAA & RWE) – Indirect Treatment Comparisons. This role designs and delivers market access analytics, supports evidence generation, and aids in analyses for Health Technology Assessment (HTA) and payer submissions. Responsibilities include leading the design and execution of indirect treatment comparisons, observational studies, and comparative effectiveness analyses, providing statistical methodology guidance, leading evidence-generation workstreams, applying advanced statistical methods, and partnering across internal functions and external partners. | — | 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 |
| Senior Medical Affairs Manager Senior Medical Affairs Manager at Johnson & Johnson in Shanghai, China, responsible for ensuring healthcare compliance, safety vigilance, providing medical information, managing clinical activities, developing relationships with external experts, and supporting product registration and business strategy within the healthcare domain. | — | 0 |
| Technology Solutions Manager, Innovative Medicine Australia (18-month fixed-term) The Technology Solutions Manager will be a key point of contact for Business Technology needs and Patient Programs across Australia and other Asia Pacific markets. This role involves supporting technology strategy, managing the delivery of local applications, overseeing financial aspects, and leading technology improvements for patient programs. The position requires experience in the pharmaceutical/healthcare industries, strong project and service management skills, and knowledge of IT compliance requirements. | — | 0 |
| Manufacturing Tech I - OTTAVA This role involves electro-mechanical assembly of robotic modules and components for surgical platforms, supporting production schedules, and ensuring compliance with medical device regulations (ISO 13485, FDA QSR). The technician will interpret procedures, conduct basic tests, identify and escalate issues, and maintain clean manufacturing standards. Responsibilities also include preparing production lines, managing material transactions, and recording build data in MES/ERP systems. Requires a high school diploma or equivalent with 0-2 years of experience in regulated industries, knowledge of GDP, and proficiency with assembly tools. | — | 0 |
| Innovative Medicine_Commercial Insight Manager This role is a Commercial Insight Manager within the Data Analytics & Computational Sciences function, focusing on Business Intelligence. The individual will contribute to the BI team by coordinating policies, procedures, and plans, supporting data aggregation and distribution using BI tools like Tableau and Power BI, and identifying opportunities to enhance the BI strategy. The role also involves collaborating with broader teams to analyze industry and geographic trends, competitor strategies, and mentoring junior colleagues. | — | 0 |
| Logistics Transportation Management Technical Product Manager Technical Product Manager for SAP Transportation Management (TM) solutions, focusing on configuration, business requirement alignment, and stakeholder liaison within Johnson & Johnson's Innovative Medicine division. Requires deep expertise in SAP TM, including BN4L and Advanced TM modules, and strong analytical and problem-solving skills. | — | 0 |
| [Quality] 信頼性保証部 カスタマーリレーションズ TSR (Telephone Service Representative)(契約社員) This role is a Telephone Service Representative in the Quality Assurance department, focusing on customer relations for the Vision Care Company. The primary responsibility is to receive, collect, and record customer complaints and quality information from the market using a global application with AI assistance. The role involves information gathering, data entry into a database, and collaborating with safety management for medical complaints. It requires customer service experience, PC skills, and strong communication abilities, with a focus on providing optimal solutions within legal and company regulations. | — | 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 |
| Sr. Site Manager (Sr. CRA - Monitor de Pesquisa Clínica Sr) - São Paulo The Sr. Site Manager (Sr. CRA) role at Johnson & Johnson is responsible for overseeing clinical trial sites, ensuring compliance with protocols, SOPs, GCP, and regulations. This role acts as the primary contact between the sponsor and the investigational site, managing activities from study start-up to closure, including site selection, monitoring, subject recruitment, and data accuracy. The position requires independent operation with minimal supervision and may involve mentoring others. | — | 0 |
| Head, Therapeutic Area Lead Rheumatology, US Medical Affairs- Immunology Johnson & Johnson is seeking a Head, Therapeutic Area Lead Rheumatology, US Medical Affairs- Immunology. This senior director role involves leading a matrixed team to develop and execute the scientific strategy and business plan for the Rheumatology Therapeutic Area. Responsibilities include overseeing evidence generation, data dissemination, clinical trial supervision (Phase 3b and 4), and collaboration with cross-functional partners. The role requires an advanced scientific degree and significant experience in clinical research and the pharmaceutical industry, with a preference for immunology/rheumatology experience. | — | 0 |
| Sr. Project Manager, Instruments & Accessories The Sr. Project Manager, Instruments & Accessories will be responsible for planning and driving the design and development execution of instruments and accessories for the Ottava surgical robotics platform. This role involves tracking document releases for regulatory submissions, developing project timelines, establishing communication processes and metrics, setting team goals, owning project risk management, and supporting change control processes. The position requires 5+ years of project management experience in complex environments, with a Bachelor's degree, and experience in product lifecycle management, risk management, change control, and document control. | — | 0 |
| Associate Clinical and Sales Specialist Associate Clinical and Sales Specialist role at Johnson & Johnson's MedTech division, focusing on Electrophysiology systems and catheter equipment. Responsibilities include achieving sales growth, building customer relationships, providing clinical and technical assistance during procedures, driving product education and adoption, managing operations, and launching new products. Requires a background in Health Sciences or Biomedical Engineering, strong business partnering and communication skills, and flexibility to travel. | — | 0 |
| EMS associate The EMS Associate, CAR-T Belgium role supports the production of CAR-T cell therapies in a cGMP-controlled cleanroom environment. Responsibilities include microbiological and aseptic oversight, contamination control, environmental monitoring program management, and supporting investigations. The role collaborates with Process Development, Quality, and Operations teams to ensure compliance with cGMP requirements and deliver life-changing therapies. | — | 0 |
| Senior Operations Assistant Distribution Centre The Senior Operations Assistant Distribution Centre role at Johnson & Johnson oversees daily warehouse and loan operations, focusing on efficient, compliant, and high-quality service delivery. Responsibilities include inventory control, SAP accuracy, equipment readiness, and cross-functional coordination, while maintaining safety standards and supporting continuous operational improvement within the Orthopaedics division. | — | 0 |
| AskGS Experience Center Associate - Japanese Bilingual This role is for a Japanese Bilingual Experience Center Associate at Johnson & Johnson, focusing on resolving global client inquiries related to HR, Payroll, Procurement, and Expense Reporting processes via phone, email, web-form, and chat. The associate will document cases, escalate complex issues, and support employees with self-service options and policy navigation. | — | 0 |
| Manager, Data Quality Operations Manager for Data Quality Operations at Johnson & Johnson, responsible for ensuring the accuracy, completeness, and consistency of data within master data management workflows. This role involves defining data standards, implementing validation rules, monitoring data health, coordinating remediation efforts, and collaborating with business and IT partners to ensure data trustworthiness for decision-making and compliance with regulatory requirements. The position focuses on process optimization, automation, and reporting on data quality KPIs within a regulated industry. | — | 0 |
| Manager, Data Quality Operations Manager for Data Quality Operations at Johnson & Johnson, focusing on ensuring the accuracy, completeness, and consistency of data within master data management workflows. This role involves defining data standards, implementing validation rules, monitoring data health, and coordinating remediation efforts, acting as a liaison between business operations and IT in a regulated healthcare environment. | — | 0 |
| Warsaw MedTEST Co-Op Co-op program participant assisting and contributing to an assigned team in the design and development of research studies for new materials, technologies, and/or products within the orthopaedic industry. Responsibilities include familiarization with R&D testing, manufacturing processes, material characterization, evaluation of processes, wear/functional/impaction studies, developing new test methods, and performing failure analyses. | — | 0 |
| Sr. Administrative Assistant Sr. Administrative Assistant role at Johnson & Johnson, supporting the Head of Global Regulatory Policy & Intelligence and leadership team. Responsibilities include managing travel, coordinating meetings and events, handling procurement, onboarding new team members, and maintaining document systems. Requires strong organizational, communication, and problem-solving skills, with proficiency in enterprise systems. | — | 0 |
| Senior Specialist, Clinical Risk Management Johnson & Johnson is seeking a Senior Specialist, Clinical Risk Management to join their R&D Quality CRM team. This role involves coordinating the identification, assessment, and mitigation of quality risks in clinical trials to ensure data integrity, patient safety, and compliance with regulatory requirements. The specialist will execute data-driven, risk-based trial oversight activities and support inspection readiness. | — | 0 |
| Senior Specialist, Clinical Risk Management Johnson & Johnson is seeking a Senior Specialist, Clinical Risk Management to join their R&D Quality CRM team. This role involves coordinating the identification, assessment, and mitigation of quality risks in clinical trials to ensure data integrity, patient safety, and regulatory compliance. The specialist will conduct data-driven, risk-based trial oversight, maintain quality plans, and support inspection readiness activities. | — | 0 |
| Senior Specialist, Clinical Risk Management Johnson & Johnson is seeking a Senior Specialist, Clinical Risk Management to join their R&D Quality CRM team. The role involves coordinating the identification, assessment, and mitigation of quality risks in clinical trials to ensure data integrity, patient safety, and regulatory compliance. Responsibilities include participating in study activities, evaluating risk mitigations, maintaining quality plans, communicating risk updates, providing guidance on quality issues, supporting inspections, and advising on research quality and compliance. | — | 0 |
| Senior Pilot Plant Engineer This role focuses on process scale-up and the application of advanced process modeling and digital solutions within pilot plants for pharmaceutical ingredient development. The Senior Pilot Plant Engineer will support New Product Introduction (NPI) projects, lead scale-up activities, and develop/deploy models to optimize pilot plant operations, integrating them into plant systems. The role requires collaboration with cross-functional teams, data engineers, and automation specialists, with a strong emphasis on process safety and quality. | — | 0 |
| Manager, Data Quality Operations Manager for Data Quality Operations at Johnson & Johnson, responsible for ensuring data accuracy, completeness, and consistency. This role involves defining data standards, implementing validation rules, monitoring data health, and coordinating remediation efforts within a regulated industry. The position requires collaboration with business operations, IT, and various supply chain functions to maintain trustworthy data for decision-making and support product launch timelines. | — | 0 |
| Senior Engineer, Materials Engineering Senior Engineer, Materials Engineering role at Johnson & Johnson Vision focused on leading raw material and process related projects for contact lens manufacturing. Responsibilities include project leadership, material characterization, supplier collaboration, and ensuring adherence to quality and regulatory standards within a medical device environment. | — | 0 |
| Staff Engineer Staff Engineer role in Supply Chain Engineering at Johnson & Johnson Vision, focusing on planning and executing change control projects, qualifying new equipment, and implementing project management methodologies. The role involves technical design reviews, supervising external teams, and resolving quality/manufacturing issues within a regulated environment. | — | 0 |
| Senior Specialist Source-to-Contract EMEA This role is for a Senior Specialist in Source-to-Contract for the EMEA region at Johnson & Johnson. The primary focus is on procurement operations, including strategic sourcing, contract negotiation, drafting, and management. The role involves collaborating with business units and category leaders, ensuring compliance, and driving continuous improvements. A key responsibility is supporting the development and implementation of automation and AI initiatives within the procurement function. | — | 0 |
| Exp Anlst Cust Qual This role focuses on processing and assessing medical device complaints to ensure compliance with global regulations. It involves analyzing data, coordinating investigations, and preparing reports related to product quality and adverse events, with a strong emphasis on regulatory requirements and quality management. | — | 0 |