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 47% 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 57 new AI-related roles. That is a -46% change versus the prior 30 days (106 → 57).
| Title | Stage | AI score |
|---|---|---|
| Regulatory Affairs Professional, Data Integrity EMEA - IDMP Project This role is responsible for managing and ensuring the integrity of regulatory data within EMEA for Johnson & Johnson's Innovative Medicine division. It involves updating regulatory tracking systems, scrutinizing data entry requests, collaborating with data owners, and supporting audits and process improvements, with a focus on IDMP project activities. | — | 0 |
| Director, Clinical Risk Management Post Approval Delivery Unit Director, Clinical Risk Management Post Approval Delivery Unit at Johnson & Johnson oversees the risk management of a Disease Area Stronghold (DAS) or development phase, ensuring coordination, identification, assessment, and mitigation of quality risks impacting trial data integrity, patient rights, safety, or well-being. The role involves providing oversight to data-driven, risk-based trial execution, ensuring compliance with regulatory requirements and internal procedures, and maintaining inspection readiness. Responsibilities include people leadership, strategic guidance on quality risk assessments, issue consultation, escalation, compliance assessment, and leading inspection readiness processes. |
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| Director, Clinical Risk Management Post Approval Delivery Unit This role oversees the overall risk management of a Disease Area Stronghold (DAS) or development phase within Johnson & Johnson's healthcare sector. The Director will work with CRM Representatives to ensure the coordination, identification, assessment, and mitigation of quality risks impacting trial data integrity, patient rights, safety, or well-being. The role also involves providing oversight for data-driven, risk-based trial execution, ensuring compliance with regulatory requirements and internal procedures, and maintaining inspection readiness. Key responsibilities include people leadership, strategic guidance on quality risk assessments, issue consultation, escalation, compliance assessment, inspection readiness and support, consultancy on research quality, and supporting post-licensing/acquisition integration. | — | 0 |
| Director, Clinical Risk Management Post Approval Delivery Unit Director overseeing clinical risk management for post-approval delivery units in healthcare. Responsibilities include managing a team, ensuring quality risk assessments, compliance with regulations, and leading inspection readiness activities. Focuses on trial data integrity, patient safety, and regulatory adherence. | — | 0 |
| Quality Assurance Associate (New Product Introduction) The Quality Assurance Associate will ensure compliance with GMP, company procedures, and regulatory requirements during new product introduction, technology transfer, and commercial launch phases. The role supports NPI activities, ensuring processes, documentation, and systems are robust and compliant for clinical and/or commercial production, contributing to site compliance and product quality, safety, and efficacy. | — | 0 |
| Scientist Biological Research (Fixed Term Contract 3 years) Scientist role in Oncology Discovery at Johnson & Johnson, focusing on identifying and validating novel therapeutic targets for lung and head and neck cancers. Responsibilities include designing and performing in vitro experiments, mammalian cell culture, and various cell-based assays. Requires a Bachelor or Masters degree and strong organizational and communication skills. | — | 0 |
| Employee Experience Specialist with Dutch Johnson & Johnson is seeking an Employee Experience Specialist with Dutch language skills to support HR-related inquiries from employees. This role involves answering questions about employee programs, services, policies, and processes, investigating issues, and detailing cases in a case management application. The specialist will collaborate with HR operations and specialist teams, with training provided for those new to HR. The position is based in Taguig, Philippines. | — | 0 |
| Employee Experience Specialist with Dutch This role is an Employee Experience Specialist in HR, supporting employees with HR-related inquiries, policies, and processes. It involves collaborating with specialist teams and providing support in multiple countries. The role requires fluent Dutch and English, customer service skills, and an interest in HR or payroll. | — | 0 |
| [MedTech] Transport & Trade Operations Manager, Integrated Supply Chain, Deliver Japan The Transport & Trade Operations Manager is responsible for managing import and export operations, ensuring compliance with regulations, monitoring KPIs, managing freight costs, and collaborating with cross-functional stakeholders. This role requires experience in supply chain management, people management, and supplier management, with a strong emphasis on trade compliance and operational efficiency. | — | 0 |
| [Innovative Medicine] Experienced Specialist, Risk Management Hematology, Local Medical Safety This role focuses on product safety and pharmacovigilance within the pharmaceutical industry, specifically managing risk management activities for J&J's Innovative Medicine portfolio in Japan. The individual will ensure compliance with local regulations and company policies, prepare and submit aggregate reports, and collaborate with cross-functional teams and health authorities. The role requires strong analytical, communication, and leadership skills, with fluency in both Japanese and English. | — | 0 |
| Programa de Prácticas (Marketing) - CDMX, México This is a Marketing Internship role at Johnson & Johnson, focusing on supporting administrative and operational tasks, collaborating on new drug launches and established product tracking, data analysis, report and presentation creation for the sales force, and market analysis. The role requires active participation in team meetings and tracking assigned tasks and activities. It also involves creating and tracking materials, events, content for the sales team, budget tracking, and market analysis to identify opportunities. | — | 0 |
| Intership Program (Legal and HCC) - Grecia, Alajuela, Costa Rica Internship program focused on Legal and Health Care Compliance (HCC) at Johnson & Johnson in Grecia, Costa Rica. Responsibilities include internal communication, training material development, audit mitigation, third-party due diligence, risk assessments, and project participation. Requires active enrollment in higher education pursuing Accounting, Finance, Law, or related fields, 40 hours/week availability, and advanced English proficiency. | — | 0 |
| Patient Solutions Program Coordinator This role focuses on the operational execution and data management of Patient Education programs within Johnson & Johnson's Innovative Medicine division. It requires a strong data-driven mindset, analytical capability, and attention to detail to ensure program consistency, quality, and compliance with regulatory standards. The coordinator will track KPIs, analyze data for insights, identify process improvements, and collaborate with stakeholders to align execution with strategic priorities. | — | 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 |
| Manager- ServiceNow Solution Architect Manager-level ServiceNow Solution Architect at Johnson & Johnson, responsible for designing and implementing scalable, secure solutions within their enterprise ServiceNow platform. The role emphasizes technical judgment, platform sustainability, and hands-on solution quality in a large-scale, highly governed environment, with a focus on configuration over customization and supporting upgrade readiness. Collaboration with platform leadership on GenAI initiatives is also mentioned. | — | 0 |
| Quality Inspector I (2nd Shift) The Quality Inspector I role at Johnson & Johnson is responsible for performing inspections, checks, and tests on incoming materials, parts, subassemblies, and finished medical devices. This includes visual, physical, mechanical, and electrical measurements, as well as documentation and data entry. The role requires attention to detail, ability to follow SOPs, and computer literacy. | — | 0 |
| Quality Inspector II (2nd Shift) The Quality Inspector II at Johnson & Johnson is responsible for performing inspections, checks, and tests on incoming materials, components, and finished medical devices. This role involves using various measurement tools, documenting inspection results, maintaining quality records, and identifying potential issues. Prior experience in quality inspection within the medical device industry is preferred, along with knowledge of relevant quality standards and regulations. | — | 0 |
| Production Associate II This role is for a Production Associate II at Johnson & Johnson, focused on manufacturing fiber optic sensors. Responsibilities include handling optical fiber, using chemicals for sheathing removal, attaching connectors with epoxy, polishing and inspecting components, cleaning optical parts, using precision equipment, assembling small components under a microscope, performing chemical tuning, and using calibrated instruments for testing. The role also involves data collection, clean room maintenance, and troubleshooting equipment. | — | 0 |
| Medical Science Liaison - Neuroscience - Schizophrenia (MD, VA, DC, DE) The Medical Science Liaison (MSL) is a field-based role responsible for developing relationships with Key thought leaders/HCPs and providing scientific and clinical information about Johnson & Johnson's neuroscience products, specifically for Schizophrenia. The role involves scientific exchange, territory execution, insight generation, and supporting investigator-initiated studies. Candidates are expected to reside in the Baltimore, Washington, DC or Northern Virginia area and possess a Doctorate level degree or equivalent experience. | — | 0 |
| J&J Operating System Senior Analyst The JJOS Senior Analyst supports the strategy, deployment, and continuous improvement of the Johnson & Johnson Operating System (JJOS) within Supply Chain Excellence (SCE). This role helps to enable the operating model execution and adoption by translating JJOS standards into usable materials and by supporting structured engagement governance to help mature the operating system. The role enables execution of the JJOS strategic roadmap by providing analytical insight, operational support, and coordination across initiatives, governance forums, and performance management processes. In addition, this role supports digital tools to translate requirements into actionable analyses, materials, reporting, and process documentation. | — | 0 |
| R&D Product Support Engineer The R&D Product Support Engineer role at Johnson & Johnson focuses on supporting R&D activities for in-house robotic endoscopy systems. Responsibilities include managing and troubleshooting mechanical, electrical, and electromechanical equipment, maintaining system configuration documentation, supporting verification and testing activities, and ensuring compliance with regulatory standards. The role requires experience in mechanical or electromechanical environments, preferably within the medical device industry. | — | 0 |
| Production Associate II Production Associate II responsible for manufacturing fiber optic sensors, including precise assembly, chemical handling, polishing, inspection, and data collection in a clean room environment. | — | 0 |
| External Planning Lead The External Planning Lead at Johnson & Johnson is responsible for strategic liaison between internal customers and external manufacturing sites for global site planning management of biologic products. This role involves defining, measuring, analyzing, and implementing planning controls and processes to ensure alignment with strategic objectives, focusing on timely deliveries, target inventory levels, and continuity of supply. Key responsibilities include setting up business plans, managing supply agreements, following global planning routines, identifying supply risks, and tracking performance indicators. | — | 0 |
| Quality Control Scientist Quality Control Scientist at Johnson & Johnson responsible for performing routine QC testing on raw materials, in-process, and finished products, including physical, analytical, and chemical testing. The role involves maintaining lab equipment, managing consumables, ensuring documentation compliance with cGMP, ISO 13485, and FDA QMSRs, and liaising with external testing organizations. Requires a BSc in a relevant scientific discipline and at least 3 years of senior quality laboratory experience in the healthcare industry. | — | 0 |
| Technology Leader - Manager Technology Leader - Manager role at Johnson & Johnson focused on supporting technology strategy and execution for Immunology. This role partners with business leaders to shape technology direction, set objectives, and prioritize demand to deliver measurable outcomes, operating in a cross-functional environment to drive innovation and continuous improvement. | — | 0 |
| Clinical Science & External Research Manager Johnson & Johnson MedTech is seeking a Clinical Science & External Research Manager to lead end-to-end evidence generation strategies for the Electrophysiology business unit. This role involves managing investigator-initiated studies, registries, and real-world evidence projects, ensuring adherence to GCPs, and collaborating with cross-functional teams and external investigators to generate clinically relevant evidence and support publication plans. The ideal candidate will have strong project management, scientific, and communication skills, with a background in clinical research and a preference for medical device experience, particularly in cardiovascular or electrophysiology. | — | 0 |
| Sr Principal Eng - Process Engineering Lead early design inputs and technical strategy for synthetic drug product manufacturing processes, focusing on oral solid dose (OSD) and innovative forms, including bioavailability enhanced technologies like amorphous solid dispersions (ASD) and spray drying. This role involves collaborating with multi-functional teams across global sites to ensure robust process design, standardization, and technology selection. | — | 0 |
| Sr Principal Eng - Process Engineering This role focuses on process engineering for synthetic drug product manufacturing, specifically oral solid dose and innovative forms, with expertise in bioavailability enhanced technologies like amorphous solid dispersions and spray drying. The Sr. Principal Engineer will lead early design inputs, technical strategy, and problem-solving for capital projects and manufacturing sites, collaborating with cross-functional teams and external partners. The role requires a Master's degree or equivalent and 10 years of relevant experience in synthetic drug product manufacturing. | — | 0 |
| Sr Principal Eng - Process Engineering The Sr Principal Engineer - Process Engineering role at Johnson & Johnson focuses on leading early design inputs and technical strategy for synthetic drug product manufacturing processes. This includes expertise in controlled bioburden-drug product manufacturing (OSD and innovative forms) and drug product intermediates with bioavailability enhanced technologies, supporting internal and external manufacturing sites. The role involves collaborating with multi-functional teams, influencing technology direction, and ensuring robust process design and standardization. | — | 0 |
| Sr. Manufacturing Engineer - Shockwave Medical This role is for a Sr. Manufacturing Engineer in the medical device industry, focusing on designing, developing, and implementing manufacturing processes, tooling, and fixtures throughout the product lifecycle. It involves collaboration with R&D, QA, and Production, process improvement using Lean principles, and ensuring compliance with quality system requirements. | — | 0 |
| Sr. Site Transfer Manufacturing Engineer - Shockwave Medical This role is for a Sr. Site Transfer Manufacturing Engineer in the medical device industry, focusing on leading and executing product and process transfers between manufacturing sites. The engineer will coordinate cross-functional teams, manage transfer plans, oversee validation and qualification, and ensure compliance with quality system regulations. The role requires experience in manufacturing engineering within a regulated environment, specifically with site-to-site transfers, process validation, and statistical methods. | — | 0 |
| Engineer Manufacturing Systems This role focuses on managing and improving manufacturing execution systems (MES) within a regulated manufacturing environment. The Engineer, Manufacturing Systems will handle change requests, coordinate workshops, document processes, develop training, and provide first-level support for shop floor users. The ideal candidate has experience with MES/ERP systems and a passion for using digital systems to optimize supply chain performance. | — | 0 |
| Director, Global Real-world Evidence (RWE) Global Commercial Strategy Organization (GCSO) Director, Global Real-world Evidence (RWE) Global Commercial Strategy Organization (GCSO) at Johnson & Johnson. This role focuses on developing and executing RWE strategies to enhance global go-to-market launch planning for oncology assets. Responsibilities include defining research questions, study design, data selection and analysis, results dissemination, and ensuring compliance. Requires a Master's degree in a quantitative field, 6+ years of experience in pharma/biotech/healthcare consulting, and expertise in observational research. Familiarity with statistical programming tools like SAS, R, or Python is required. | — | 0 |
| Senior Quality Engineer Senior Quality Engineer at Johnson & Johnson, focusing on quality engineering oversight for the manufacture of capital systems, particularly complex electro-mechanical, software-controlled systems for medical applications. Requires experience with medical device regulations (ISO 13485, ISO 14971, 21 CFR 820), equipment qualifications, process validations (IQ/OQ/PQ), and test method validations. | — | 0 |
| Product Quality Vigilance, E2E Supervisor The Product Quality Vigilance (PQV) E2E Supervisor at Johnson & Johnson is responsible for overseeing a team that manages the end-to-end product quality vigilance process, including complaint intake, triage, investigation, issue escalation, trending, and reporting. This role ensures activities conform to current standards, procedures, and regulatory requirements, and supports quality initiatives and improvement programs. | — | 0 |
| Manager - Planning Systems & Capability Manager role focused on supply chain planning systems and capability development within Johnson & Johnson's Innovative Medicine division. The role involves owning demand intake, standardizing global planning processes, automating and integrating processes, and enabling system project execution. Requires a Bachelor's degree and 6+ years of experience in supply chain planning or systems implementation. | — | 0 |
| Product Quality Vigilance, E2E Supervisor This role is a supervisor for Product Quality Vigilance (PQV) at Johnson & Johnson, focusing on the end-to-end complaint handling process for healthcare products. It involves overseeing a team of analysts, ensuring adherence to quality standards and regulatory requirements, managing investigations, and reporting on product quality data. The role requires collaboration with various internal and external stakeholders and ensuring compliance with corporate policies and regulatory agency requirements. | — | 0 |
| Manager – Planning Systems & Capability Manager role focused on developing and deploying V2V planning capabilities within the supply chain organization. This involves driving process decomposition, aligning system requirements with business needs, and partnering across teams to deliver integrated global solutions. Responsibilities include owning demand intake, standardizing processes, supporting platform operations, and enabling system project execution. | — | 0 |
| Medical Science Liaison Johnson & Johnson is seeking a Medical Science Liaison (MSL) for their Haematology franchise in South East England. This field-based role involves providing scientific and medical support to Key Opinion Leaders and internal teams, sharing knowledge to optimize brand and medical strategy, and gathering insights. The role requires strong academic/healthcare/industry background, resilience, a passion for healthcare, and the ability to learn quickly, assimilate information, build relationships, and communicate data concisely. Critical thinking, project management, business insight, prioritization, problem-solving, and cross-functional collaboration are also essential. | — | 0 |
| Medical Science Liaison Johnson & Johnson is seeking a Medical Science Liaison (MSL) for their Oncology franchise. This field-based role involves providing scientific and medical support to Key Opinion Leaders, sharing knowledge to optimize brand and medical strategy, and gathering insights for the Medical Affairs team. The role requires strong academic/healthcare/industry background, resilience, passion for healthcare, ability to learn quickly, assimilate information, build relationships, critical thinking, project management, business insight, prioritization, problem-solving, and collaboration skills. | — | 0 |
| Analyst Quality Control, 3rd shift (2 positions) Quality Control Analyst role at Johnson & Johnson focusing on microbiological testing and monitoring in a biosynthetic facility. Responsibilities include environmental monitoring, various laboratory tests (BET, Bioburden, Sterility), supporting investigations, and ensuring GMP compliance in pharmaceutical manufacturing. | — | 0 |
| ELEC MECH ASSEMBLER II This role is for an Electro Mechanical Assembler II at Johnson & Johnson's MedTech division. The primary responsibility is to assemble electromechanical products according to documented procedures and specifications, perform dimensional measurements, conduct tests, and document work performed. The role requires experience with electrical, electronics, IT, or mechanical equipment, interpreting schematic diagrams, and knowledge of manufacturing principles. Experience in a regulated industry is preferred. | — | 0 |
| Principal Embedded Software Test Engineer - Abiomed Principal Embedded Software Test Engineer for a medical device company (Abiomed) focusing on cardiovascular solutions. Responsibilities include leading test plan development, execution of manual and automated tests for embedded software, collaborating with engineering teams, enhancing test automation frameworks and CI/CD pipelines, and mentoring junior members. Requires experience with embedded platforms, real-time operating systems, Python scripting, and understanding of FDA cybersecurity guidelines. Medical device industry experience is strongly preferred. | — | 0 |
| Sr Embedded Software Test Engineer - Abiomed Senior Embedded Software Test Engineer for medical devices, focusing on developing and executing manual and automated test plans, enhancing test automation frameworks and CI/CD pipelines, and performing root cause analysis. Requires experience with embedded platforms, real-time operating systems, Python scripting, and familiarity with cybersecurity guidelines and DevOps tools. | — | 0 |
| Lead Project Analyst (PMO) This role is for a Lead Project Analyst in Global Compensation COE at Johnson & Johnson. The primary focus is on managing end-to-end projects related to year-round and year-end compensation processes, utilizing J&J FPX methodologies and Lean Six Sigma for process optimization and operational excellence. Key responsibilities include coordinating cross-functional teams, managing project plans, improving processes, enhancing documentation, and ensuring timely delivery of compensation programs globally. The role also involves supporting governance, managing survey participation, salary structure development, market pricing, and coordinating with HRIS/Workday and other partners. Experience with compensation processes, project management tools, and a complex global organization is required. | — | 0 |
| Lead Project Analyst Lead Project Analyst for Global Compensation COE at Johnson & Johnson, responsible for driving high-impact projects in compensation processes, process optimization, risk mitigation, and operational excellence. Requires strong project management, FPX experience, and preferred Lean Six Sigma certification. Role involves coordinating cross-functional teams, executing project plans, improving processes, and ensuring delivery of compensation programs globally. | — | 0 |
| Quality Engineer This role is a Process Quality Engineer in the Supply Chain Engineering function at Johnson & Johnson. The primary focus is on maintaining and developing the Quality System for site manufacturing processes, ensuring compliance with ISO 9000, ISO13485, FDA QSRs, and the Medical Devices Directive. Responsibilities include trending non-conformances, investigating issues, identifying root causes, leading investigations, partnering with engineering on new processes, owning validation master plans, supporting maintenance activities, and working on process improvement. The role requires a degree in science or engineering, at least 3 years of experience in a regulated industry, and knowledge of quality systems and tools. A demonstrated understanding of AI concepts and prompt generation is also mentioned. | — | 0 |
| Process Microbiologist The Plant Microbiologist owns and integrates contamination control within operations by translating microbiological risks into practical controls, investigations, and continuous improvement programs across the plant. This role reports to the Sr. Director Biotherapeutics Operations and partners closely with Operations, the Centre of Expertise (CoE), and Quality. The position has no direct reports but provides dotted-line leadership to operations project leads and the Contamination Prevention Team, serving as the single point of contact (SPOC) for contamination control in Operations. | — | 0 |
| Sr. Demand Planner The Senior Demand Planner role at Johnson & Johnson is responsible for leading US Demand Planning and the Integrated Business Planning (IBP) process for the Surgery team. This includes business planning, coordinating US inventory strategy, driving service management and product allocations, and identifying/leading digital initiatives to improve efficiency and data quality. The role requires a Bachelor's degree, 2 years of related experience, and proficiency in MS Office and ERP/MRP systems. | — | 0 |
| Senior Director, Global Cost, Service & Repair Senior Director, Global Cost, Service & Repair leader responsible for end-to-end service and repair supply chain strategy and execution across a global, multi-site network. Drives availability, speed, cost, and quality of repaired/refurbished medical devices through integrated planning, service supply, repair operations enablement, logistics, inventory management, and supplier performance. Partners closely with Quality, Regulatory, Operations, Engineering, Finance, and Commercial teams to ensure compliance and customer experience while delivering measurable improvements in service levels and gross margin/margin rate. Identifies and implements capabilities (systems, analytics, network design, and standard work) that provide competitive advantage and scalable growth. Accountable for Service & Repair supply chain performance in Danvers, Aachen, DE, and Japan locations. Focuses on Abiomed’s global cost improvement focused on driving Abiomed Gross Margin Improvements. Builds team to work with Abiomed Finance, Ops, and Quality to drive overall product and process improvements that will deliver meaningful cost savings targeted at driving gross margin improvements. | — | 0 |