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 69 new AI-related roles. That is a -37% change versus the prior 30 days (109 → 69).
| Title | Stage | AI score |
|---|---|---|
| Global MT SC ERP Quality Manager The Quality Manager will support the MedTech SC Digital Transformation organization, focusing on modernizing supply chain digital capabilities by harmonizing ERP systems and standardizing business processes. This role will ensure the SAP S/4HANA ERP platform has the necessary support structures, processes, and governance for Quality Management. Responsibilities include serving as a primary contact for the Quality business area, building partnerships with stakeholders, supporting SAP QM process sustainment, collaborating on quality assurance policies, identifying and remediating system issues, coordinating testing, supporting security role design, managing enhancement intake, and contributing to the continuous improvement of the support model. | — | 0 |
| Sr RA Professional This role is in Regulatory Affairs, focusing on product submissions and registration within Johnson & Johnson's healthcare sector. Responsibilities include reviewing and documenting product inserts, package labels, and artwork, maintaining labeling E2E activity tracking systems, and supporting local labeling initiatives. The role requires collaboration with various cross-functional teams to ensure labeling processes comply with local regulations and global standards. |
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| 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 |
| Process Engineer Process Engineer at Johnson & Johnson in Limerick, Ireland, responsible for planning, executing, and delivering engineering activities within a manufacturing value stream. This role involves technical leadership to improve safety, quality, delivery, and cost, supporting new product introductions, process changes, and compliance in a highly regulated (GMP/ISO/FDA) environment. Key responsibilities include managing change control, validation (IQ/OQ/PQ), technical investigations, and driving continuous improvement initiatives in collaboration with cross-functional teams. | — | 0 |
| [Innovative Medicine] E2E Demand & Supply Planner (Fixed-term) Johnson & Johnson is seeking an E2E Demand & Supply Planner for their Innovative Medicine division in Seoul. This role focuses on integrated demand and supply planning, supporting IBP/S&OP processes, managing risks, and enabling data-driven planning. Responsibilities include demand forecasting, supply planning, inventory management, E2E integration, risk management, cross-functional coordination, and process improvement using planning tools. | — | 0 |
| Production Planning Manager Production Planning Manager at Johnson & Johnson responsible for Master Planning, Scheduling, and Inventory management in a plant, ensuring customer service and compliance with regulatory requirements. The role involves managing inventory, supporting capacity plans, supervising production scheduling, and collaborating with other departments. Requires leadership experience in the pharmaceutical/biotech/medical industry and ERP knowledge. | — | 0 |
| 地方政府事务及市场准入地区经理 This role focuses on market access and reimbursement for Johnson & Johnson's products within a specific region in China. Responsibilities include establishing relationships with government bodies, navigating healthcare policy for product inclusion in medical insurance catalogs, managing tender processes, and exploring innovative access models like commercial insurance. The role also involves communication with regulatory affairs and supporting other cross-functional initiatives. | — | 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] Regulatory Affairs Intern Intern role supporting the Regulatory Affairs team in day-to-day activities related to registration, lifecycle management, and regulatory compliance within the pharmaceutical industry. Responsibilities include assisting with regulatory submission documents, labeling reviews, and ad hoc projects like regulatory intelligence research. | — | 0 |
| Experienced I Stat Programmer Experienced Statistical Programmer responsible for developing, verifying, and documenting code for clinical data analysis and reporting within the pharmaceutical industry. Supports clinical projects and submissions with a focus on quality and timeliness. | — | 0 |
| Manutentore Elettrico - Manufacturing This role is for an Electrical Maintenance Technician at a Johnson & Johnson manufacturing site in Latina, Italy. The primary responsibilities include performing preventive, corrective, and predictive maintenance on production and packaging machinery, supporting process improvement, recording activities in SAP-CMMS, interpreting equipment manuals, and applying safety and quality procedures. The role requires a technical diploma, preferably with prior experience as an electrical maintenance technician, and knowledge of electrical diagrams, diagnostic tools, programmable logic systems, and basic English. | — | 0 |
| MSL Hematolgía - Noreste (Residencia Cataluña) Medical Science Liaison (MSL) role focused on communicating scientific and medical information about company products to healthcare professionals in the Hematology therapeutic area in Spain. The role involves staying updated on scientific advancements, building relationships with key opinion leaders, and providing data-driven insights to support product value and market access discussions. This is not an AI/ML role. | — | 0 |
| Associate Marketing Director, SEAI, Oncology The Associate Marketing Director for SEAI Oncology at Johnson & Johnson is responsible for developing and executing strategic business plans to achieve sales growth and volume objectives within the therapeutic area. This role involves shaping strategy, coaching commercial teams, identifying resources, monitoring expenses, and leveraging analytics and market insights to inform decisions. The position also requires cross-functional collaboration, driving brand performance, leading marketing teams, and managing product lifecycles, including launch readiness. | — | 0 |
| E&PS Senior Manager, Project Management Senior Manager, Project Management for Engineering & Property Services (E&PS) at Johnson & Johnson, responsible for managing a portfolio of key projects supporting business operations and compliance initiatives within a regulated manufacturing environment. This role involves leading the planning, execution, and delivery of site capital and design/construction projects, ensuring they meet safety, quality, and budget standards. | — | 0 |
| Field Service Engineer, GBA Field Service Engineer responsible for onsite service, maintenance, and technical support for DePuy Synthes robotics systems and related digital platforms, ensuring system uptime, regulatory compliance, and customer satisfaction. This role involves installation, commissioning, preventive maintenance, troubleshooting, and customer training within hospital and laboratory environments. | — | 0 |
| Principal R&D Project Manager The Principal R&D Project Manager will plan and execute projects within the Navigation platform in Digital R&D, ensuring delivery against scope, schedule, cost, and quality in a regulated medical device environment. This role involves managing cross-functional teams, project budgets, risks, and design controls to achieve predictable delivery outcomes. | — | 0 |
| Complaint Quality Approver (2 openings) This role is for a Complaint Quality Approver at Johnson & Johnson, responsible for reviewing and approving complaint records to ensure investigations are complete, scientifically justified, and compliant with regulations. The role involves confirming risk assessment, root cause analysis, and proper documentation before complaint closure, with a focus on a regulated healthcare environment. | — | 0 |
| Business Unit Manager - Immunology Business Unit Manager for Immunology at Johnson & Johnson, responsible for directing and leading the Country Value Team (CVT) in sales and marketing, developing and implementing strategies to maximize demand and achieve the business plan for the Immunology portfolio. This role involves people management, P&L management, and strategic planning within the pharmaceutical industry. | — | 0 |
| Analyst Quality Control The Quality Control Analyst is responsible for conducting biochemical, microbiological, and/or general testing of final product samples submitted to the QC laboratories, ensuring compliance with procedures, standards, and GMP regulations. This role involves performing analytical testing, data review, documentation, and supporting inspections within the biopharmaceutical industry. | — | 0 |
| Scientist, Translational Oncology Scientist role focused on designing, executing, and analyzing preclinical experiments in translational oncology to understand target expression, tumor biology, and mechanisms of response/resistance for compounds in clinical development. Requires strong laboratory skills in cell and molecular biology techniques, data analysis, and collaboration within a matrixed environment. | — | 0 |
| NPI Test Engineer/Surgical Robotics-OTTAVA This role focuses on developing and deploying test software solutions to support the manufacturing of complex electro-mechanical components within a medical robotics system. It involves designing automated test algorithms, building scalable software infrastructure, and ensuring high standards of repeatability and validation. The position also supports troubleshooting, root cause analysis, and data-driven insights to improve manufacturing processes, while collaborating cross-functionally with design, manufacturing, and data teams in a regulated MedTech environment. | — | 0 |
| MSAT Experienced Scientist The MSAT Experienced Scientist at Johnson & Johnson is responsible for the build, development, and lifecycle management of manufacturing and packaging equipment cleaning processes within the pharmaceutical industry. This role involves leading and supporting cleaning validation activities, developing strategies, coordinating cross-functional efforts, performing risk-based evaluations, and driving continuous improvement initiatives. The position requires a Bachelor's degree with 4+ years of experience or an advanced degree with 2+ years of experience in MSAT, validation, or related technical support within a regulated industry. | — | 0 |
| Process Engineer Process Engineer role at Johnson & Johnson focused on supply chain engineering, specifically process engineering. Responsibilities include project management, PLC-based control system design and installation, equipment reliability, and coordinating activities. The role requires investigating product inquiries, implementing corrective actions, and building expertise in relevant technologies. Compliance with quality management systems (ISO 13485, ISO14001, OSHAS18001) and performing process validations are key duties. Experience with PLCs, vision systems, CIM, robotics, and automation is preferred. | — | 0 |
| R&D Electrical Engineer I - Shockwave Medical R&D Electrical Engineer I at Johnson & Johnson focused on developing innovative medical devices for cardiovascular disease treatment. Responsibilities include mixed-signal analog and digital circuit design, microcontroller and FPGA integration, schematic capture, PCB layout, prototype testing, and ensuring compliance with medical device standards and design controls. | — | 0 |
| Ingeniero de Embalaje - Contrato Plazo Indefinido Packaging Engineer role at Johnson & Johnson, focusing on generating packaging material specifications, managing official packaging lists, coordinating material functionality tests, and ensuring compliance with regulatory standards. Requires a degree in a scientific or engineering field, 1-2 years of experience in pharmaceutical, food, or chemical industries, and proficiency in Microsoft Office, Minitab, SAP, and Project. | — | 0 |
| Senior Principal Scientist, Large Molecule Drug Product Scientific Integrator Senior Principal Scientist role focused on end-to-end scientific integration for late-stage large-molecule drug product programs within the pharmaceutical industry. Responsibilities include leading cross-functional teams, defining drug product strategy, authoring regulatory submissions, and supporting manufacturing. Requires significant experience in biopharmaceutical development and CMC regulatory strategy. | — | 0 |
| Manufacturing Technician III The Manufacturing Technician III role at Johnson & Johnson focuses on operating, adjusting, and maintaining fully automated production lines in a manufacturing environment. Responsibilities include troubleshooting equipment failures, performing routine maintenance, investigating root causes of non-conformances, and participating in process improvement initiatives. The role requires technical skills in areas like PLC systems, electro-mechanical devices, and robotics, with an emphasis on maintaining safety, quality, and production guidelines. | — | 0 |
| Sr. Service Innovation Engineer This role is for a Senior Service Innovation Engineer in the MedTech division, focusing on product development, lifecycle management, and technical support for service solutions. The engineer will act as a liaison between technical groups and service departments, recommend design for serviceability, manage service procedures, and provide escalation support for complex technical issues. The role requires experience in regulated industries and project lifecycle management. | — | 0 |
| Senior Maintenance Technician Senior Maintenance Technician role at Johnson & Johnson in Leiden, Netherlands, focusing on ensuring the reliability and continuity of production and utility systems in a pharmaceutical manufacturing environment. Responsibilities include troubleshooting, maintenance, service, and optimization of equipment, adhering to GMP and safety regulations, and working within a 5-shift system. Requires MBO 4 level education in electrical engineering or measurement and control technology, with proven industrial experience. | — | 0 |
| Global Neuroscience Market Access Co-Op This role supports global health economics and market access tactical plans for neuroscience brands/portfolio, develops tools for market access strategies, and conducts literature searches for clinical/real-world data. It is a co-op position for students pursuing a degree in a relevant field. | — | 0 |
| MES SPECIALIST I This role is for an MES Specialist I at Johnson & Johnson, focusing on the Manufacturing Execution System (MES) and connected systems. Responsibilities include supporting shopfloor control, managing change requests, performing impact assessments, maintaining SOPs, mapping processes, writing documentation, training users, and participating in system configuration, testing, validation, and implementation. The role also involves monitoring interfaces, participating in QA non-conformities and CAPA actions, and ensuring compliance with health, safety, and environmental practices. The position requires a technical background, experience in system integration testing and user problem understanding, and strong communication skills. Knowledge of GMP, ISO, FDA regulations, SQL, and programming tools is preferred. | — | 0 |
| Senior Principal Scientist, Discovery-Immunology Senior Principal Scientist, Discovery Immunology role at Johnson & Johnson focused on leading discovery-stage research programs, translating complex biology into therapeutic hypotheses, and mentoring a team of scientists. Requires a Ph.D. in Immunology or related discipline with 5-7 years of drug discovery experience. | — | 0 |
| Senior Director, Therapeutic Area Lead, Mood – US Medical Affairs, Neuroscience Senior Director, Therapeutic Area Lead, Mood – US Medical Affairs, Neuroscience at Johnson & Johnson. This role defines and executes the scientific strategy for the mood portfolio, focusing on data generation, dissemination, and pre-launch initiatives. It involves leading a high-performing team, collaborating cross-functionally, and managing relationships with external experts. The position requires deep expertise in mood disorders and pharmaceutical industry experience, with a strong emphasis on leadership and people management within a regulated healthcare environment. | — | 0 |
| Marketing Intern,Neuroscience Johnson & Johnson is seeking a Marketing Intern in Istanbul, Turkey, to support the Neuroscience portfolio. The role involves assisting with marketing activities, brand plan implementation, material approval, monitoring material utilization, developing CLM materials, enhancing insight generation through BI tools and market research, tracking brand performance, and engaging with external stakeholders. The ideal candidate is a university student in Business Administration or Economics with a passion for marketing and strong communication skills in English and Turkish. | — | 0 |
| Maintenance Technician This role is for a Maintenance Technician in a pharmaceutical manufacturing environment, responsible for ensuring the reliability and continuity of production and utility systems. The job involves troubleshooting, maintenance, service, and optimization of equipment, with a strong emphasis on GMP, safety, and compliance. | — | 0 |
| Senior Injection Moulding Engineer Senior Injection Moulding Engineer role focused on providing polymer processing and engineering expertise for medical devices and pharmaceutical products. Responsibilities include project delivery, equipment and process design/installation, troubleshooting, and leading cross-functional teams for new product introductions, all within a regulated quality management system. | — | 0 |
| Therapeutic Area Manager, Medical Information Scientific Engagement This role focuses on engaging healthcare professionals in scientific dialogue, developing materials for medical information requests, and analyzing customer insights within the pharmaceutical industry. It involves handling inquiries, creating patient scientific content, providing escalation support, and conducting scientific training. | — | 0 |
| Principal Scientist The Principal Scientist will conduct research aimed at the development of therapeutic agents, originating scientific experiments, developing new methodologies, and maintaining state-of-the-art scientific knowledge. This role involves guiding and training external CROs, maintaining a lab presence, and actively participating in lab work. The scientist will also be responsible for summarizing, interpreting, and drawing conclusions from data, preparing technical reports, and publishing work where appropriate. They will apply scientific knowledge to projects, introduce new techniques, establish priorities, and keep abreast of scientific developments. Additionally, the role involves advising on resources, planning developmental opportunities for personnel, and participating in research discussions. | — | 0 |
| Staff Project Engineer Staff Project Engineer responsible for executing site-wide capital projects for manufacturing platforms and supporting systems in a regulated medical device industry. This includes equipment upgrades, product brand conversions, and new line installation/commissioning, with a focus on budget adherence, schedule execution, and technical expertise. Requires experience with formal project management tools, leading multi-functional teams, and ensuring compliance with FDA/Safety/Quality policies. | — | 0 |
| Cryopreservation Mfg Operator, CAR-T Operates manufacturing equipment and executes tasks in a cGMP environment for cryopreservation of CAR-T products. Responsibilities include cell culturing, purification, aseptic processing, and documentation according to SOPs and regulations. Requires a high school diploma with 4 years of relevant experience or a Bachelor's degree with 0-2 years of experience. | — | 0 |
| Post-Doctoral Scientist Emerging Technologies Post-doctoral scientist role focused on developing and validating continuous manufacturing concepts for biologics drug product, integrating advanced analytics, Process Analytical Technology (PAT), and data-driven approaches for real-time monitoring and control. The role involves hands-on lab work, experimental design, data analysis, and collaboration with R&D, engineering, and quality teams to advance technologies towards GMP readiness. | — | 0 |
| Senior NPI Engineer (m/f/d) Senior NPI Engineer responsible for supplier and process engineering activities for new product introductions, focusing on robust industrialization, supplier readiness, process validation, and risk management in a regulated healthcare environment. | — | 0 |
| Experienced RA professional Lifecycle Submission This role is for an Experienced RA Professional in Lifecycle Submissions within Johnson & Johnson's Innovative Medicine division, based in Cairo, Egypt. The primary focus is on coordinating and executing lifecycle management procedures for pharmaceutical products, ensuring timely submissions, implementation of changes, and database updates in compliance with country-specific requirements and health authority approvals. The role involves strategic planning for submissions, preparing documentation, and acting as a Subject Matter Expert for regulatory affairs. | — | 0 |
| Principal R&D Project Manager The Principal R&D Project Manager will be responsible for planning and executing projects within the Navigation platform in Digital R&D, ensuring delivery against scope, schedule, cost, and quality in a regulated medical device environment. This role involves coordinating cross-functional teams, managing project budgets, risks, and communications, and driving disciplined design controls and phase-gate readiness. | — | 0 |
| Sr R&D Program Manager Senior R&D Program Manager for Power Tools portfolio within Digital R&D at Johnson & Johnson. This role provides platform-level program leadership for electro-mechanical orthopaedic solutions, integrating multiple product and technology initiatives, platform priorities, cross-functional dependencies, and governance mechanisms. The role operates as a senior cross-functional leader across various departments to drive prioritization, product roadmap decisions, release planning, tradeoff recommendations, integrated execution, and executive visibility in a regulated medical device environment. | — | 0 |
| Senior RA Specialist, Program Lead, EPNV Senior Regulatory Affairs Specialist and Program Lead at Johnson & Johnson, responsible for coordinating regulatory activities, defining strategies for new product introductions and lifecycle management, managing submissions and post-approval actions, and ensuring databases are current. The role involves leading RA specialists, liaising with cross-functional teams and health authorities, and monitoring regulatory changes to ensure compliance and timely product approvals. Requires knowledge of local and international regulations, analytical and problem-solving skills, and experience in regulatory environments, particularly with complex devices. | — | 0 |
| Technical Service Product Leader This role is for a Technical Service Product Leader in the MedTech Cardiovascular division at Johnson & Johnson. The primary focus is on representing Technical Service interests throughout project phases, defining service requirements, managing deliverables, analyzing field feedback, and improving service documentation for new products. The role requires collaboration with R&D, QA, and project management teams, with a strong emphasis on compliance and regulatory standards. | — | 0 |
| Finance Leadership Development Program Johnson & Johnson is seeking recent graduates for its 30-month Finance Leadership Development Program (FLDP). This program offers rotational assignments in various finance and accounting areas across the company's businesses and locations, along with formal training and coaching to develop future finance leaders. Participants will gain experience in areas like Financial Planning and Analysis, Commercial Finance, Supply Chain Finance, R&D Finance, General Accounting, Treasury, and Global Audit & Assurance. | — | 0 |
| Analyst Contract & Processing Services, Bogotá, Colombia. Individual contributor role focused on contract and processing services within Johnson & Johnson's procurement function. Responsibilities include supporting program implementation, contributing to projects, performing simple trend analysis, and drafting responses related to departmental procedures. Requires a degree in Law, Business Law, or Business Administration with at least 2 years of experience in contract management. | — | 0 |