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 57 new AI-related roles. That is a -46% change versus the prior 30 days (106 → 57).
Currently tracking 49 active AI roles, down 47% versus the prior 4 weeks. Primary focus: Agent · Engineering. Salary range $77k–$283k (avg $144k).
| Title | Stage | AI score |
|---|---|---|
| Associate Maintenance Engineer Associate Maintenance Engineer role focused on supporting maintenance technicians, coordinating projects, managing SOPs, and ensuring compliance with GMP and EHS regulations within a manufacturing environment. Requires a Bachelor's degree in engineering and strong analytical and communication skills. | — | 0 |
| Stage MSAT Internship role supporting Manufacturing Science and Technology (MSAT) at Johnson & Johnson's Latina, Italy plant. Responsibilities include supporting manufacturing process changes, project management for continuous improvement and customer-specific requirements, and data analysis. | — | 0 |
| Health Economics, Market Access & Reimbursement Manager - Lung & Solid Tumors The Health Economics, Market Access & Reimbursement Manager will develop and execute market access strategies in Italy for lung cancer and solid tumors, lead health economic evaluations, design real-world evidence initiatives, and manage pricing and reimbursement strategies, including dossier submissions to AIFA. |
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| Senior Facility Technician This role is for a Senior Facility Technician at Johnson & Johnson in Suzhou, China. The primary responsibilities include maintaining facility systems (clean room, water systems, electrical, etc.), buildings, and pipe systems in good working condition. The technician will execute preventive maintenance (PM) and work orders, ensure compliance with EHS policies and local regulations, and support quality system development. The role also involves guiding junior technicians, identifying cost/efficiency improvements, and participating in technical audits and other assignments. | — | 0 |
| Sr. Manager CQV Johnson & Johnson is seeking a Sr. Manager CQV (Commissioning & Qualification) to lead CQV activities in large capital projects, ensuring compliance with regulatory and quality standards. The role involves strategy development, planning, execution, and handover, with a focus on risk-based qualification and digital validation tools. | — | 0 |
| Senior Strategy & Business Transformation Manager This role is for a Senior Strategy & Business Transformation Manager at Johnson & Johnson in Mumbai, India. The primary focus is on shaping and driving the strategic agenda for JJIM India, including leading commercial strategy development, business insights generation, and transformation projects. It also involves supporting the SEAI Cluster on Haematology portfolio strategy. The role requires strong analytical, problem-solving, and stakeholder management skills, with advanced proficiency in Excel and PowerPoint. Experience in strategy consulting or a similar in-house role is preferred, as is exposure to the pharma/healthcare commercial strategy. | — | 0 |
| Quality Assurance Technician I Quality Assurance Technician I responsible for in-process and final product quality analyses/inspection in compliance with standards and regulatory requirements, interpreting and evaluating analyses against specifications. Identifies quality issues, prevents production issues, and suggests improvements. Uses measuring devices and testing equipment to accept or reject products. Audits manufacturing processes and outputs against internal and regulatory standards. Reports deviations and defects. Requires minimum one year inspection experience, blueprint reading, electrical/mechanical inspection knowledge, understanding of QSR/ISO requirements, and ASQ-CQIA certification. | — | 0 |
| Medical Science Liaison Oncology, Riyadh Medical Science Liaison Oncology role to be located in Riyadh, Saudi Arabia. The purpose is to maximize company product value through high scientific quality communication with Leading Specialists on a peer-to-peer basis. Through activities in line with the Medical Affairs Plan, the MSL is jointly responsible for the realization of short-term and long-term company goals. To be a therapeutic area scientific expert in Genitourinary Oncology (Prostate and bladder cancers), responsible for discussing our products, patients’ treatment trends and studies in the therapeutic areas in which we are involved, on a peer-to-peer basis with defined audience of Leading Specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other partners) and to be considered a trusted scientific counterpart. | — | 0 |
| MRO & Indirect Materials Planner, Orthopedics The MRO & Indirect Materials Planner is responsible for ensuring the availability, control, and cost-effective management of Maintenance, Repair, and Operations (MRO) and other indirect materials required to support uninterrupted operations. This role owns inventory strategies, purchasing execution, and supplier coordination for indirect materials, balancing service levels with working capital and compliance requirements. | — | 0 |
| Specialist, Source-to-Contract - Americas This role supports the implementation and execution of the organization's strategic sourcing plan, including contract negotiation, authoring, and management. It also involves driving continuous improvements and supporting automation and AI initiatives within the Source-to-Contract (S2C) function, acting as a product owner for S2C tools and AI features. | — | 0 |
| Senior Clinical Programming Lead Senior Clinical Programming Lead at Johnson & Johnson, responsible for leading clinical trial programming activities, including data models for reporting and CDISC submission packages. Focuses on creating efficiencies and ensuring data quality and consistency across trials. | — | 0 |
| Regulatory Affairs Analyst The Regulatory Affairs Analyst role at Johnson & Johnson supports regulatory activities for medical device approvals and clearances in the US and European markets. Responsibilities include preparing, submitting, tracking, and archiving official documents, collaborating with global regulatory affairs partners and functional teams, and ensuring compliance with international regulations. | — | 0 |
| Commercial Operations Site Lead - Miami, FL-Johnson & Johnson MedTech - Orthopaedics Commercial Operations Site Lead for Johnson & Johnson MedTech's Orthopaedics division in Miami, FL. This role involves leading a sales support team to drive sales growth, manage inventory efficiently using advanced analytics, and act as a liaison between Sales, Customer Service, Finance, and Supply Chain for order management. Responsibilities include processing local inventory, supporting field sales, managing inventory replenishment and expiry, monitoring outbound metrics, and collaborating with supply chain partners. | — | 0 |
| Director, External Innovation, Neuroscience Johnson & Johnson is seeking a Director, External Innovation, Neuroscience to identify and secure external licensing and collaboration opportunities to enhance their internal discovery efforts in Neuroscience. The role involves working cross-functionally to assess and shape external opportunities, manage a pipeline of assets, and engage with external partners in biotech, pharma, and academia. The position requires a PhD in Neuroscience research or significant pharmaceutical R&D experience, a strong track record in drug discovery, and expertise in neurodegenerative, neuropsychiatric, or ophthalmology diseases. | — | 0 |
| Quality LIMS Administrator The Quality LIMS Administrator role at Johnson & Johnson is responsible for managing and maintaining the Laboratory Information Management System (LIMS) for two Medtech sites. This includes user provisioning, configuration, supporting change control, and ensuring compliance with local procedures and regulatory requirements. The role also involves supporting standardization of LIMS governance, system enhancements, user acceptance testing, and documentation. The administrator will use data to identify risks and improvement opportunities, implement mitigations, and escalate issues. This is a support role within the Quality Control department, focused on system administration and process improvement. | — | 0 |
| Senior Industrial Engineer Senior Industrial Engineer at Johnson & Johnson in Santa Clara, CA, focused on leading and implementing manufacturing systems, process improvement, and capacity/layout design for electro-mechanical and robotic medical device assembly. The role involves process design and validation, labor/capacity modeling, optimization, cost reduction, and mentoring junior engineers, with a strong emphasis on Lean, Six Sigma, and medical device regulatory compliance. | — | 0 |
| Sr. Administrative Assistant This is a Sr. Administrative Assistant role in the Hematology DAS team at Johnson & Johnson, supporting global development functions and business support projects. The role involves managing complex calendars, coordinating meetings, handling confidential information, processing expenses, and leading/supporting business support projects. It requires a minimum of 4 years of administrative experience and proficiency in Microsoft Office. | — | 0 |
| Senior Package Development Engineer (Orthopedics) Senior Package Development Engineer for Orthopedics (Trauma) at Johnson & Johnson (DePuy Synthes). Role involves participating in audits, providing technical expertise for risk assessments and compliance assurance, ensuring robust and compliant packaging solutions, leading troubleshooting for packaging issues, and maintaining knowledge of industry and regulatory trends. Requires a Bachelor's degree in engineering or equivalent, 4-6 years of experience in packaging, experience in a regulated environment, and project management skills. | — | 0 |
| Associate Site Manager - Buenos Aires This is an entry-level Associate Site Manager role in Clinical Trial Support at Johnson & Johnson's Innovative Medicine division. The role involves managing investigational sites, ensuring trial activities are conducted according to SOPs, monitoring site performance, managing data accuracy, and ensuring compliance with regulatory requirements. It requires collaboration with various stakeholders and adherence to strict timelines and documentation standards. | — | 0 |
| Medical Science Liaison, GU Oncology - Ontario, Canada Johnson & Johnson is seeking a Medical Science Liaison (MSL) for their GU Oncology team in Ontario, Canada. This role focuses on executing the Medical Affairs Plan by serving as a point of contact for Key Opinion Leaders (KOLs) and Healthcare Professionals (HCPs) in the territory. Responsibilities include developing and implementing scientific engagement plans, cultivating relationships with KOLs, engaging in scientific exchange, staying updated on scientific literature and clinical data, collecting KOL insights, assisting in the interpretation of clinical trial outcomes and real-world data, participating in medical forums, providing clinical consultation to business partners, supporting clinical development programs, and assisting with investigator-initiated studies and compassionate drug requests. A Pharm D, PhD, or MD is required, along with a strong clinical/scientific background, excellent communication and interpersonal skills, project management abilities, and business acumen. | — | 0 |
| Manager, External Manufacturing Manager for External Manufacturing Supply Integration (EMSI) at Johnson & Johnson's DePuy Synthes, focusing on managing global external manufacturers for the Enabling Tech platform. Responsibilities include seamless supply integration, business continuity, quality, compliance, supplier OTIF, tactical and continuous improvement initiatives in planning, NPI, and technical operations, and leading issue resolution. The role also involves managing, coaching, and developing a team. | — | 0 |
| Manager, External Manufacturing Manager for External Manufacturing Supply Integration (EMSI) at Johnson & Johnson's DePuy Synthes Supply Chain, focusing on managing global external manufacturers for the Enabling Tech platform. Responsibilities include seamless supply integration, ensuring business continuity, quality, compliance, and supplier OTIF. The role involves managing tactical and continuous improvement initiatives in planning, NPI, and technical operations, resolving supplier issues, and leading a team. Requires a BA/BS degree, 6+ years of experience in supplier management, planning, or manufacturing operations, preferably in medical devices, and strong cross-functional collaboration skills. | — | 0 |
| R&D Engineer 2 - Electrophysiology R&D Engineer 2 at Johnson & Johnson focused on the design, development, verification, and manufacturing transfer of electrophysiology and ultrasound catheter products. The role involves mechanical and mechatronic design, collaboration with cross-functional teams, and adherence to design controls in a regulated medical device environment. | — | 0 |
| Engineer I Innovation Excellence Entry-level engineering role focused on product development, testing, validation, and documentation within the MedTech industry, with a strong emphasis on regulatory compliance and collaboration. | — | 0 |
| Lead Senior Administrative Assistant This role provides high-level administrative and operational support to senior leaders within the Treasury organization, including the Assistant Treasurer, Chief Investment Officer, and the Benefit Investments and Operations leadership team. Responsibilities include managing complex calendars, coordinating meetings, processing travel and expenses, overseeing office operations, supporting onboarding/offboarding, and ensuring compliance with company policies and regulatory requirements. | — | 0 |
| Associate Director Discovery- Oncology Associate Director for Oncology Discovery at Johnson & Johnson, focusing on characterization and development of cancer therapeutics through in vivo pharmacology studies. Responsibilities include leading a team, designing and interpreting experiments, and collaborating across functions. Requires expertise in oncology drug development, team leadership, and in vivo study design. | — | 0 |
| Associate Marketing Director - Surgical Vision, Sydney Associate Marketing Director for Surgical Vision at Johnson & Johnson in Sydney. This role involves developing and executing strategic marketing plans, overseeing product management, driving market share and profitability growth, and building relationships with key opinion leaders. Requires marketing/product management experience in medical devices, preferably Ophthalmology or Capital Equipment. | — | 0 |
| Customer Engagement Platform Manager The Customer Engagement Platform Manager will lead the business ownership, adoption, and evolution of existing and next-generation field engagement platforms. This role focuses on integrating face-to-face and digital engagement into a cohesive customer experience, driving continuous digital experience evolution, and managing the collaboration between business partners and technical teams to define product requirements. The role involves defining product vision and roadmaps, enabling integrated customer experiences, driving adoption of scalable ways of working, establishing feedback loops for insights, leading local rollouts of new CRM and engagement capabilities, and owning business-side platform management. | — | 0 |
| Sr. Manager, Trade Markets This role is for a Sr. Manager in Greece for DePuy Synthes, a Johnson & Johnson company. The primary focus is on supporting business operations, strategy execution, and organizational effectiveness within the Greek market. The role involves partnering with cross-functional teams, analyzing performance metrics, ensuring compliance, and supporting transformation initiatives. It is a business management and operations role within the healthcare industry, not directly related to AI/ML development. | — | 0 |
| Sr. Manager GBS, Manila This role is a Sr. Manager GBS in Human Resources, specifically an HR Business Partner, at Johnson & Johnson. The posting mentions a planned separation of the Orthopaedics business and potential future employment with the new entity, DePuy Synthes. The role focuses on HR functions and does not involve AI/ML development. | — | 0 |
| Sr. Manager, SEA NA This role is for a Sr. Manager, SEA NA in Human Resources at Johnson & Johnson, focusing on supporting business operations, strategy execution, and organizational effectiveness across Southeast Asia and North Asia markets. It involves partnering with stakeholders, analyzing business performance, supporting planning and forecasting, ensuring compliance, and managing change initiatives. The role also includes administrative tasks related to document handling and records management. The required qualifications include a Bachelor's degree and 8-10 years of experience in business management or related fields, with a preference for experience in regulated industries or specific Asian markets. | — | 0 |
| Senior Supply Chain Project Specialist This role is responsible for the planning, alignment, and execution of Supply Chain activities for approved projects, including new product introductions, product line extensions, network optimization, and lifecycle management. The position requires collaboration with various internal teams and business partners to ensure project objectives are met, utilizing project management excellence and LEAN methodology. | — | 0 |
| Experienced I Statistical Programmer Experienced Programmer (ST05) in Integrated Data Analytics and Reporting (IDAR) to support data analyses and reporting activities within trial activities. This role is responsible for the design and development of programs in support of clinical research analysis and reporting, ensuring CDISC compliance, and collaborating with cross-functional teams. Requires 2+ years of programming experience, preferably in Pharma/CRO/Biotech, with knowledge of SAS (preferred), R, or Python, and basic understanding of regulatory guidelines (ICH-GCP). | — | 0 |
| National Scheduling Assistant Manager This role is a National Scheduling Assistant Manager in the Supply Chain Deliver function, specifically within Warehouse & Distribution at Johnson & Johnson. The primary focus is on supporting operational delivery of the National Scheduling team, driving daily/weekly/monthly cadences, solving operational problems, delivering reporting, and leading continuous improvement. The role involves leading daily operations, acting as a first-line escalation point, establishing planning cadences, driving continuous improvement through root-cause analysis and process optimization, and collaborating cross-functionally to lead, coach, and develop the scheduling team. While the role mentions 'adoption of digital/automation solutions', it does not indicate AI/ML as a core craft. | — | 0 |
| EAMA AM This role focuses on researching and analyzing national and local medical insurance policies, tracking trends, and assessing their impact on the medical device industry. The individual will develop company strategies for medical insurance, identify market opportunities, manage policy risks, conduct internal policy training, support government affairs, and collaborate with industry stakeholders. The role requires a Master's degree or higher in public health, medical insurance management, or pharmaceutical policy, with experience in government affairs, policy research, or market access within the medical device or pharmaceutical industry. Strong analytical, research, reporting, and strategic planning skills are essential, along with excellent communication and collaboration abilities. | — | 0 |
| Manager, WW Professional Education, Robotics Manager, WW Professional Education, Robotics at Johnson & Johnson is responsible for developing and delivering professional education content for surgical robotic systems, including hands-on training and curriculum development. The role involves collaboration with R&D, Marketing, and external partners, and adherence to regulatory requirements. | — | 0 |
| Senior Business Analyst, Medical Affairs This role focuses on designing, delivering, and optimizing reporting and analytics solutions for Medical Affairs within Johnson & Johnson. The Senior Business Analyst will be responsible for enabling transparency in business and field performance, operational and compliance oversight, and monitoring grants and giving through scalable reporting frameworks, dashboards, and analytics products. The role involves end-to-end delivery from requirements gathering to data management, extraction, transformation, modeling, and visualization, aiming to provide clear visibility into business performance, compliance adherence, and operational impact. The candidate will also drive continuous improvement, manage reporting solutions as a portfolio, and explore advanced analytics and reporting technologies, including AI, to enhance automation and transparency. | — | 0 |
| Senior Design Quality Engineer Senior Design Quality Engineer at Johnson & Johnson's MedTech division, focusing on supporting new product development and sustaining activities within a regulated healthcare environment. Responsibilities include ensuring compliance with regulations, managing product risk, cybersecurity, change controls, and design controls throughout the product development lifecycle. | — | 0 |
| Sr. Data Engineer This role focuses on enabling self-service analytics and developing high-quality dashboards, reports, and data models in Power BI. The Sr. Data Engineer will partner with business stakeholders to translate analytical needs into robust, scalable semantic models and intuitive dashboards, driving decision-making. The role involves data modeling in Power BI, DAX, working with Snowflake, and collaborating with other data engineering tools. | — | 0 |
| Manager Scheduling, Advanced Therapies Manager of Scheduling for Advanced Therapies at Johnson & Johnson, focusing on leading a team of schedulers for CAR-T slot scheduling across US manufacturing sites. The role emphasizes team leadership, operational execution, and schedule reliability to ensure accurate slot allocation and patient material flow. Responsibilities include people management, overseeing scheduling execution, operational coordination with various departments, issue resolution, performance tracking, and ensuring compliance with safety, quality, and cGMP standards. Requires a Bachelor's degree and 6 years of experience in scheduling, supply chain, or manufacturing operations, with familiarity in ERP/MRP or scheduling systems. Experience in regulated environments (GMP) and people leadership is preferred. | — | 0 |
| Programa de Estágio 2026 São Paulo | Jurídico Internship program for the Legal department at Johnson & Johnson in São Paulo, Brazil. The role involves supporting the legal team with contractual matters, corporate governance, and daily administrative tasks within the legal department. The intern will gain practical experience in an in-house corporate legal environment, supporting lawyers and internal clients across Latin America. Key responsibilities include assisting with contract review, organizing legal documentation, and maintaining legal databases. Requires active university student status with a graduation date between August 2027 and August 2028, advanced English proficiency, and availability for a hybrid work model. | — | 0 |
| Sr. Regulatory Affairs Professional Johnson & Johnson is seeking a Sr. Regulatory Affairs Professional to support drug development programs and marketed products. This role involves advising regulatory teams, preparing submissions, interacting with regulatory agencies, and ensuring compliance with regulatory requirements within the pharmaceutical industry. | — | 0 |
| QA Validation Specialist II LVV QA Validation Specialist II LVV at Johnson & Johnson, providing quality oversight for production of analytical cell banks, cryopreservation, and viral vector testing in a cGMP environment. Responsibilities include reviewing environmental monitoring data, verifying GMP and ISO cleanroom standards, evaluating contamination control, documenting validation activities, supporting investigations, overseeing equipment/facility/process qualification (IQ/OQ/PQ), and Computerized System Validation (CSV). | — | 0 |
| Case Manager, PSC Johnson & Johnson is seeking a Case Manager for their Patient Service Center (PSC) to handle inquiries about patient programs, referral status, benefits verification, and financial assistance. This client-facing role involves supporting Healthcare Providers (HCPs) and patients, managing program enrollment, processing requests, and ensuring clear communication and access to therapy. The role requires strong customer service skills and the ability to manage a caseload efficiently. | — | 0 |
| Field Medical Advisor Field Medical Advisor for Immunology in Greece, responsible for scientific engagement with healthcare professionals, medical education, clinical research support, and providing medical information. Requires advanced life sciences degree and experience in medical affairs. | — | 0 |
| Senior Specialist, Source-to-Contract-NA This role is a Senior Specialist in Source-to-Contract (S2C) within the Healthcare Professional (HCP) Contracting team at Johnson & Johnson. The primary focus is on the operational execution of contracting processes for Marketing, Research, and Clinical Development categories. Key responsibilities include managing daily operations of the HCP Contracting Team, reviewing contract requests, drafting and negotiating agreements, ensuring compliance with policies, and supporting automation and AI initiatives. The role requires a Bachelor's degree and a minimum of 3 years of professional experience in HCP contract drafting, review, and negotiation, with 4-6 years of relevant experience in Procurement, Finance, or Legal within the pharmaceutical/life sciences industry. | — | 0 |
| Clinical Training Mgr Monarch This role is for a Clinical Training Manager for the Monarch program at Johnson & Johnson. The primary responsibilities include facilitating technical and clinical training for physicians and their staff, supporting initial procedures and advanced training, and collaborating with sales and customer success teams. The role also involves supporting commercial education programs and providing product demonstrations. It requires experience educating clinicians on complex medical devices and strong communication skills. | — | 0 |
| Sr Anlst Contract Serv This role is for a Senior Analyst of Contract Services in Procurement at Johnson & Johnson, focusing on IT categories. The role involves managing the source-to-contract process, including negotiation, contract drafting, and supplier relationship management. While the role supports automation and AI initiatives, its core function is procurement and contract services, not direct AI/ML development. | — | 0 |
| Senior Regulatory Affairs Specialist - Vision Senior Regulatory Affairs Specialist for Johnson & Johnson's Vision division, focusing on product lifecycle management, regulatory strategy development, submissions (e.g., 510k), compliance, and labeling review for medical devices. Requires experience in regulated environments and interaction with regulatory bodies like the FDA. | — | 0 |
| Manager, Patient Reported Outcomes Manager, Patient Reported Outcomes role at Johnson & Johnson, focusing on developing PRO strategies to measure patient experience and support product value in the drug development process. Responsibilities include conducting research, managing outsourced projects, developing training materials, and standardizing evidence communication. Requires a Master's degree with 4+ years of experience or a Bachelor's with 6+ years, including R&D understanding and project management. Experience in PROs is preferred. | — | 0 |