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.
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).
Currently tracking 49 active AI roles, down 50% versus the prior 4 weeks. Primary focus: Agent · Engineering. Salary range $77k–$283k (avg $144k).
| Title | Stage | AI score |
|---|---|---|
| Regional Medical Manager Immunology LATAM Regional Medical Affairs Manager for Immunology pipeline assets in LATAM, responsible for shaping and executing regional medical strategy, evidence generation, scientific leadership, and cross-functional integration for pre-launch and launch readiness. | — | 0 |
| Director, Wound Closure & Healing, Life Cycle Management R&D - MedTech Director of R&D, Life Cycle Management (LCM) for Wound Closure & Healing (WCH) products. Responsible for leading a team that maintains a ~$3.6B product portfolio, addressing compliance needs, and developing value creation opportunities like new claims and applications. This role involves leading LCM governance, claims strategy, operating model redesign, talent development, and driving cultural change. Requires a BS in Engineering/Science. | — | 0 |
| Staff Industrial Engineer Staff Industrial Engineer role focused on implementing business improvement initiatives for manufacturing lines, analyzing data, designing line flows, and improving business processes using Lean and Six Sigma methodologies. Responsibilities include capacity modeling, collaborating with cross-functional teams, and mentoring junior members. Requires experience in process/quality improvements, data analysis software, Lean/Six Sigma techniques, project management, and product cost knowledge. |
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| Director, R&D, Healing and Core Technology – MedTech Director of R&D, Healing and Core Technology for MedTech at Johnson & Johnson, focusing on wound closure and healing innovations. The role involves leading cross-functional teams in design, materials selection, and process development for medical devices, translating scientific concepts into regulatory-ready products, and managing project budgets and timelines. Requires strong leadership, project management, and technical expertise in biomedical engineering or materials science within the medical device industry. | — | 0 |
| Manager, Materials Engineering Manager for Materials Engineering at Johnson & Johnson, focusing on R&D Product Development within the MedTech division. The role involves leading a team of engineers, driving process standardization across multiple sites, and applying materials engineering expertise to support product delivery, business continuity, and cost improvement initiatives. Requires strong technical skills in injection molding, polymer materials, and mold fabrication, along with leadership and cross-functional collaboration. | — | 0 |
| Product Security Manager The Product Security Manager will implement Johnson & Johnson's enterprise Product Security strategy and framework for the Vision medical device portfolio. Responsibilities include supporting new product development, reviewing security requirements, recommending design solutions, conducting threat modeling, penetration testing, code analysis, and managing post-market security for marketed devices. This includes monitoring vulnerabilities, assisting with remediation, responding to customer questionnaires, and reviewing contractual agreements. The role also involves driving adherence to the Product Security framework, creating metrics, and enforcing governance. | — | 0 |
| Senior Manager, Global CAPA Management Senior Manager, Global CAPA Management role at Johnson & Johnson, focusing on ensuring the implementation and global improvement of investigation and corrective and preventive action (CAPA) processes within the Innovative Medicines sector. This role involves liaison with technical teams for QMS platform development, continuous improvement of the CAPA QMS platform, and leadership in change management and quality system integration. The position requires ensuring compliance with GxP and other regulatory requirements. | — | 0 |
| Medical Scientific Liaison (MSL) - CDMX Johnson & Johnson is seeking a Medical Scientific Liaison (MSL) for their Oncology team in Mexico City. The role involves building scientific relationships with clinical leaders, educating on evidence-based treatments, preparing the market for therapeutic innovations, and gathering strategic insights. The ideal candidate will have a medical or biomedical degree, strong scientific communication skills, and a commitment to a full-time career in the company. | — | 0 |
| Senior Quality Specialist This role is responsible for leading and supporting Global Compliance activities related to change control and document control processes within Johnson & Johnson's healthcare sector. It involves providing subject matter expertise for integrating new projects into enterprise systems, enhancing system capabilities, and troubleshooting electronic systems like EDMS/PLM. The specialist will analyze metrics, identify process improvements, develop global procedures, and ensure compliance with regulatory requirements, partnering cross-functionally to maintain audit readiness. | — | 0 |
| Transcend Senior Manager Business Test Validation Seeking a Senior Manager for Business Test Validation to drive end-to-end testing cycles for SAP S/4HANA releases within a regulated pharmaceutical environment. This role involves establishing a global testing methodology, leading cross-functional teams, and ensuring compliance with GxP and CSV standards. | — | 0 |
| Senior Quality Engineer (NPD) Senior Quality Engineer for New Product Development in the medical device industry, focusing on ensuring compliance with GMP, ISO, and other applicable standards throughout the product lifecycle. Responsibilities include developing requirements, verification/validation strategies, risk management, and documentation review. | — | 0 |
| Service and Repair Sr. Quality Engineer Quality Engineer role focused on supporting Service and Repair operations within the healthcare industry, ensuring compliance with J&J standards, regulations, and quality systems. Responsibilities include managing escalations, non-conformances, CAPA, change control, and supporting audits. | — | 0 |
| Transcend Senior Manager Business Test Validation This role is for a Senior Manager of Business Test Validation for a global business transformation program modernizing foundational transactional processes into a standardized SAP S/4HANA ERP platform within a regulated pharmaceutical environment. The role focuses on driving end-to-end testing cycles, including integration testing, Business Simulation Testing (BST), user acceptance testing (UAT), performance testing, and validation activities, ensuring alignment with GxP and CSV compliance standards. | — | 0 |
| Senior Manufacturing Engineer Senior Manufacturing Engineer at Johnson & Johnson's Limerick site, supporting a high-volume, fully automated manufacturing environment. Responsibilities include the design, installation, and improvement of lens production processes and equipment, troubleshooting, leading cost and technical improvements, project management, and ensuring quality and safety compliance within an FDA-regulated environment. | — | 0 |
| Quality Process Lead This role is for a Quality Process Lead at Johnson & Johnson, focusing on the execution and management of global Stop Shipments. Responsibilities include coordinating stakeholders, providing ERP support, managing product traceability, handling batch information, revising procedures, and supporting investigations and audits within a quality management system. The role requires experience in a quality environment and with ERP systems, with preferred knowledge of ISO and FDA standards for medical products. | — | 0 |
| Director, Public Affairs, US Oncology Johnson & Johnson is seeking a Director, Oncology Public Affairs to lead the development and execution of strategic public affairs and advocacy initiatives for their U.S. Oncology business. This role involves identifying and advancing opportunities to strengthen the external environment for their in-market portfolio and pipeline, focusing on patient access and long-term growth. The individual will act as a strategic partner, building relationships with internal and external stakeholders, including business leaders, government affairs, patient advocacy groups, and professional societies. Key responsibilities include developing and implementing public affairs strategies, advancing policy positions, leveraging platforms to strengthen the company's voice, building stakeholder networks, and managing sensitive issues. The role requires a deep understanding of business strategy, access dynamics, and the policy landscape. | — | 0 |
| Maintenance Engineering Manager, Machine Shop & Asset Management Johnson & Johnson MedTech is seeking a Maintenance Manager to lead Maintenance, Machine Shop, and Asset Management teams to ensure safe, reliable, compliant, and cost-effective manufacturing operations. The role involves developing maintenance strategies, overseeing machine shop operations, managing asset lifecycle, and partnering with other departments to maximize equipment performance. Responsibilities include leading teams, managing budgets, ensuring compliance, and coordinating breakdown responses. | — | 0 |
| Senior Quality Clerk The Senior Quality Clerk at Johnson & Johnson supports activities related to the Quality System, including managing defect tracking, document retention, records management, and product evaluations. This role also involves supporting Non-Conformance (NC) and Corrective and Preventive Action (CAPA) processes, generating reports, assisting with audits, and ensuring compliance with Good Manufacturing Practices (GMP), ISO, and QSR requirements. The position requires experience in quality control and administrative support within a regulated environment. | — | 0 |
| Programador de Produccion y Transferencias( Fixed - Term 6 Months) This role is responsible for managing the flow of raw materials and finished products in manufacturing areas, ensuring materials are handled according to production line procedures. Key responsibilities include programming production orders, balancing production lines, communicating between departments to prevent material shortages, managing production priorities, performing cycle counts, assigning components, and reconciling production orders to avoid financial impact. The role also involves managing specific product components and ensuring accurate inventory levels. | — | 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 |
| Associate Director, Regulatory Medical Writing, Oncology Associate Director, Regulatory Medical Writing, Oncology role at Johnson & Johnson. This position involves leading the writing and coordination of complex clinical and regulatory documents, setting functional tactics and strategy, and potentially managing a team of medical writers. The role requires a strong understanding of regulatory guidelines and best practices within the pharmaceutical industry, specifically in oncology. | — | 0 |
| MedTech Supply Chain Procurement Co-Op This is a co-op position supporting the MedTech Supply Chain Procurement Organization at Johnson & Johnson. The role involves enhancing project portfolio processes, supporting technology design and adoption, exploring digital tools for procurement and supplier collaboration, developing PMO strategies, tracking KPIs, and applying data-driven insights to sourcing decisions. The ideal candidate is an undergraduate student pursuing a degree in business, engineering, supply chain, or a related field, with strong analytical skills and technological curiosity. | — | 0 |
| Medical Science Liaison-Neuroimmunology, South Central Johnson & Johnson Innovative Medicine is seeking a Medical Science Liaison-Neuroimmunology for the South Central region (Texas, Louisiana, Oklahoma). The role involves providing scientific and clinical information to healthcare professionals and opinion leaders, staying updated on therapeutic area trends, and supporting research. The MSL will build external relationships, develop territory strategic plans, and conduct all activities compliantly. Requires a PharmD, PhD, MD, NP, or PA with relevant experience and travel. | — | 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 |
| Junior Oncology Medical Science Liaison - São Paulo Johnson & Johnson is seeking a Junior Oncology Medical Science Liaison in São Paulo, Brazil. This role involves building relationships with healthcare professionals (HCPs), discussing treatments, and gathering medical insights to inform medical strategy. Key activities include conveying treatment value, shaping medical practice, responding to scientific inquiries, and executing educational events. Requires a scientific background, technical English, and significant travel. | — | 0 |
| Senior Director, Lean Excellence Senior Director of Lean Excellence at Johnson & Johnson Vision, responsible for applying Lean Methodology and similar tools (Six Sigma, Lean) to drive significant business improvements in manufacturing site operational models. This includes developing and executing a multiyear roadmap, coaching team members and leaders, and creating a continuous improvement culture. | — | 0 |
| Medical Science Liaison Johnson & Johnson is seeking a Medical Science Liaison in Casablanca, Morocco. This field-based role involves scientific expertise, building relationships with healthcare professionals and key opinion leaders, generating medical insights, and supporting medical affairs strategy. The role requires strong scientific and clinical expertise, excellent communication, insight gathering, and adherence to compliance frameworks. | — | 0 |
| Eng Project Engineering - Fixed Term 24 months Project Engineering role at Johnson & Johnson focused on driving global initiatives for product families manufactured across multiple sites. Responsibilities include leading cross-functional teams, managing technical projects, solving challenges, and ensuring compliance with GMP and regulations. Requires a Bachelor's in Engineering with at least 1 year of experience in equipment/packaging/product engineering and project management, with a strong understanding of manufacturing processes and GMPs. | — | 0 |
| Operator I This role is an Operator I at Johnson & Johnson in Suzhou, China. The primary responsibilities include supporting daily production management, operating machines safely and effectively to ensure high efficiency, maintaining traceability of materials and products, balancing materials according to production plans, and completing quality records and production line activities. The role requires adherence to all applicable laws, regulations, and company procedures related to health, safety, and environmental practices. | — | 0 |
| Principal Scientist Process Johnson & Johnson is seeking a Principal Scientist to lead late-stage process development, technology transfer, and validation for biotherapeutic fill/finish manufacturing. This role requires expertise in scale-down models, process parameter evaluation, technical project management, and ensuring compliance with regulatory and cGMP standards. The scientist will act as a subject matter expert for audits and partner with cross-functional teams to define scientific strategies for new product introductions. | — | 0 |
| Operator I This role is an Operator I at Johnson & Johnson in Suzhou, China. The primary responsibilities include supporting daily production management, operating machines safely and effectively to ensure high efficiency, maintaining traceability of materials and products, balancing materials according to production plans, and completing quality records and production line activities. The role requires adherence to all applicable laws, regulations, and company procedures related to health, safety, and environmental practices. | — | 0 |
| Operator I This role supports daily production management in a manufacturing environment, focusing on operating machines safely and efficiently, maintaining traceability, balancing materials, and completing quality records and production line activities. It requires adherence to production specifications and company regulations. | — | 0 |
| Operator I Operator I role at Johnson & Johnson in Suzhou, China, focusing on supporting daily production management, operating machinery safely and efficiently, ensuring traceability, and collaborating with engineers on machine settings. Responsibilities include production work, quality record completion, and line maintenance. | — | 0 |
| Operator I Operator role at Johnson & Johnson focused on supporting daily production management, operating machinery safely and efficiently, ensuring traceability, and collaborating with engineers on machine settings. Responsibilities include production work, quality record completion, and line cleaning. This role is not directly related to AI/ML development. | — | 0 |
| Operator I Operator I role at Johnson & Johnson in Suzhou, China, focused on supporting daily production management, operating machinery safely and efficiently, maintaining traceability, and collaborating with engineers on machine settings. Responsibilities include following production schedules, completing quality records, and performing line cleaning activities. | — | 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 |
| 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. | — | 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 |
| 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 |