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 |
|---|---|---|
| [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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Senior Manager, R&D Software Engineering Senior Manager, R&D Software Engineering for a medical device Vision team, leading a team in the development of safety-critical medical device applications and embedded software systems. Responsibilities include guiding architecture, design, development, integration, and ensuring compliance with regulatory standards like FDA 21 CFR Part 820 and IEC 62304. The role involves project management, talent development, and hands-on troubleshooting. | — | 0 |
| Medical Director, Gastroenterology Therapeutic Area, US Medical Affairs Medical Director role in Gastroenterology Therapeutic Area, US Medical Affairs at Johnson & Johnson. Focuses on developing and executing clinical study programs, evidence generation plans, and contributing to regulatory submissions for GI pipeline and approved products. Collaborates with cross-functional teams to shape clinical and economic value narratives and ensure alignment with business objectives and regulatory standards. | — | 0 |
| Senior Manager Clinical Operations Johnson & Johnson is seeking a Senior Clinical Research Manager to manage a team of Local Trial Managers, Site Managers, and Clinical Trial Assistants. The role focuses on trial delivery in oncology, site engagement, staff development, training, onboarding, and resource management. Responsibilities include overseeing trial execution from feasibility to close-out, ensuring quality, timelines, and compliance with SOPs, HCC, and local regulations. The role also involves contributing to country strategy, optimizing ways of working, driving innovation, and continuous improvement. | — | 0 |
| Regional Manager - SCG North Regional Manager for Johnson & Johnson's Strategy & Corporate Development team, focusing on expanding strategic accounts and building long-term partnerships within the healthcare sector. The role involves developing business strategies, identifying market opportunities, and collaborating with various internal and external stakeholders to drive growth and ensure compliance. | — | 0 |
| PI Lead Lead PI Engineer role in Supply Chain Engineering at Johnson & Johnson, focusing on the Aveva PI system for manufacturing automation. Responsibilities include configuring interfaces, ensuring compliance with cG(a)MP, leading projects, developing global standards, and transforming the site with digital technology. Requires a Bachelor's degree in engineering and 6+ years of experience in a GxP regulated environment, with specific experience in Aveva PI. | — | 0 |
| Senior Manager, Technical Product Owner – End-to-End Anaplan Integration Senior Manager, Technical Product Owner for End-to-End Anaplan Integration role at Johnson & Johnson. Focuses on owning and optimizing the Anaplan platform, ensuring availability, performance, and operational resilience. Involves partnering with Finance, Technology Services, and other teams to translate business priorities into technical solutions, manage integrations, and enforce governance and security. Requires deep Anaplan expertise and cross-functional leadership. | — | 0 |
| Supervisor, Quality Control Microbiology Supervisor for Quality Control Microbiology department at Johnson & Johnson in Schaffhausen, Switzerland. Responsibilities include leading a team of up to 10 employees, ensuring smooth operation of microbiological laboratory activities, driving quality improvements, supporting investigations, and ensuring inspection readiness. Requires a degree in a related scientific field, several years of experience in microbiology quality control in regulated environments, and strong communication skills. Fluency in German and English is required. | — | 0 |
| Technicus This role is for a Medical Device Technician at Johnson & Johnson in Amersfoort, Netherlands. The technician will be responsible for performing pre- and post-tests on medical devices, troubleshooting technical issues, disassembling and assembling devices, documenting work in Salesforce, and managing spare parts inventory. The role requires technical experience, attention to detail, a collaborative mindset, and proficiency in English. Experience with Salesforce and MS Office is a plus. | — | 0 |
| Duales Studium Wirtschaftsingenieurwesen Duales Studium Wirtschaftsingenieurwesen (Dual Study Program in Industrial Engineering and Management) at Johnson & Johnson in Norderstedt, Germany. This program combines theoretical studies with practical experience in various business and technical areas of the company, including business excellence, quality, pricing, production, logistics, and sales. The role focuses on learning business and technical operations within a healthcare company. | — | 0 |
| Senior Scientist Clinical Pharmacokinetics The Senior Scientist Clinical Pharmacokinetics (PK Scientist) role is responsible for end-to-end Phase 1 study execution, including protocol development, pharmacokinetic/pharmacodynamic data analysis, and generating reports for clinical study reports and regulatory submissions. The role also supports other study phases with non-compartmental analysis and mentors junior scientists. | — | 0 |
| Senior Scientist Clinical Pharmacokinetics This role focuses on clinical pharmacokinetics (PK) and pharmacodynamics (PD) analysis for drug development studies, from Phase 1 through Phase 4. Responsibilities include protocol development, data analysis (specifically non-compartmental analysis - NCA), generating reports for clinical study reports (CSRs) and regulatory submissions, and mentoring junior scientists. The role requires collaboration with various departments and adherence to SOPs and regulatory requirements. | — | 0 |
| Manufacturing Operator Johnson & Johnson is seeking Manufacturing Operators for their new Lenti Viral Vector Facility in Sassenheim, Netherlands. The role involves supporting the installation and operation of new equipment, performing process and GMP documentation, and working safely in a BSL2 environment under GMP and EHS standards. The position requires experience in biotech or biopharma manufacturing, preferably with an MBO 4 or HBO education in a relevant field. | — | 0 |
| [Innovative Medicine] 生産物流本部 富士工場 オペレーションスタッフ This role is for an Operations Staff member in pharmaceutical manufacturing at Johnson & Johnson's Fuji plant in Japan. The primary responsibilities include leading inspection, manufacturing, and preservation operations according to correct procedures to ensure continuous production of quality products. The role involves managing production schedules, driving operational efficiency, safety, and quality control, and actively participating in factory improvement initiatives. Compliance with GMP and other regulations is critical. Experience with GMP/CGTP, Lean, or Six Sigma is preferred. | — | 0 |
| [Innovative Medicine] Specialist, Quality System 3 Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant) This role is a Specialist in Quality System within the Quality Operations Department at Johnson & Johnson's Fuji Plant. The primary responsibilities include managing GMP/GCTP activities such as risk assessments, investigations, CAPA, and change control. The role also involves supporting other team members, troubleshooting deviations, and leading or supporting improvement initiatives. A degree in Pharmacy, physics and chemistry, or biology is preferred, along with over 5 years of experience in quality control, quality assurance, or regulatory compliance in the pharmaceutical industry. Knowledge of GMP/GQP/QMS quality systems and business-level English proficiency are also desired. | — | 0 |
| Principal Scientist(MSAT)首席科学家-常州/苏州/上海 The Principal Scientist (MSAT) at Johnson & Johnson provides technical support for New Product Introduction (NPI), Life Cycle Management (LCM), process improvements, and new technology deployment within the Supply Chain Manufacturing division. This role involves technical assessment, due diligence, onboarding, process fit assessment, managing tech transfers, leading characterization and PPQ batches, and supporting regulatory audits. The scientist will also contribute to process optimization, cleaning validation, and cross-contamination assessments, ensuring operational discipline, safety, and quality. | — | 0 |
| Team Lead, Source Quality Team Lead for Source Quality Engineering role at Johnson & Johnson, focusing on applying quality engineering tools and methods (Six Sigma, Lean) to new product introductions, process improvements, risk management, root cause analysis, and quality control plans. The role involves mentoring and supervising junior engineers. | — | 0 |
| [HR] Talent Acquisition Contract/契約社員 [MedTech] This is a Talent Acquisition role at Johnson & Johnson's MedTech division in Tokyo, Japan. The role focuses on sourcing and managing the end-to-end recruitment process for sales and other positions. It requires direct sourcing experience, strong administrative skills, proficiency in MS Office and Workday, and the ability to analyze recruitment data. Fluency in Japanese is essential, with English proficiency preferred for reading emails and system interfaces. The role involves collaboration with hiring managers and HRBPs, candidate assessment, offer management, and ensuring a smooth onboarding process. | — | 0 |
| Principal – Third Party Cyber Risk Assessment This role is for a Principal - Third Party Cyber Risk Assessment at Johnson & Johnson. The individual will serve as a senior technical authority and thought leader for third-party cyber risk assessments across the company's global ecosystem of vendors, SaaS providers, and strategic partners. Responsibilities include performing and leading risk assessments, evaluating technical controls, identifying and documenting cyber issues, driving automation, communicating results to senior leaders, and enhancing assessment processes. The role requires a bachelor's degree in a relevant field, 5+ years of direct third-party cybersecurity risk assessment experience, and proficiency with ServiceNow GRC. Foundational knowledge of regulatory requirements is preferred. | — | 0 |
| Principal – Third Party Cyber Risk Assessment This role focuses on assessing and managing cyber risks associated with third-party vendors and partners within a large healthcare organization. It involves technical reviews of security controls, risk evaluation, and driving process improvements and automation in third-party risk assessments. The position requires strong analytical skills, experience with GRC tools like ServiceNow, and the ability to translate technical findings into business impact. | — | 0 |
| [IT] Order to Cash (O2C) Product Manager-Contract/契約社員 [Shockwave] Product Manager for Oracle Order to Cash (O2C) functionalities, focusing on design, implementation, and support of Order Management & Invoicing within Oracle Cloud ERP. Requires experience with Oracle Cloud implementations, specifically in Order Management, Billing, Account Receivable, Customer Master Data, and Pricing. Must also have knowledge of integrating Oracle Cloud with CRM applications like Salesforce and collaborate with Salesforce IT teams. The role involves translating business needs into scalable solutions, working with customer service and finance stakeholders, managing integrations with 3PL partners, and ensuring continuous system improvement. | — | 0 |
| Director, Oncology Pre-Approval Access Johnson & Johnson Innovative Medicine is seeking a Director, Oncology Pre-Approval Access (PAA) Project Owner. This role is responsible for obtaining funding and program approval, developing treatment guidelines, and managing country exit plans for Oncology PAA programs. The Director will collaborate closely with various cross-functional stakeholders including R&D, Medical Affairs, Regulatory Affairs, and Legal to ensure timely and compliant delivery of these programs. | — | 0 |
| (Jr.) Category Manager (m/f/d) This role is for a Category Manager for Direct Materials at Johnson & Johnson, focusing on procurement and strategic sourcing for medical device components. It involves developing sourcing strategies, managing supplier relationships, and ensuring compliance within the supply chain. The role does not involve AI/ML development or research. | — | 0 |
| [Innovative Medicine] Analyst, Operational Quality Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant) This role supports manufacturing operations from a quality perspective, ensuring compliance with GMP/GCTP, safety, and corporate policies. Responsibilities include supporting and overseeing operations, addressing manufacturing issues, facilitating process improvements, supporting regulatory inspections, and making batch release decisions. The role also involves creating/updating procedures, completing training, and promoting quality culture. | — | 0 |
| [Quality] Senior Manager Commercial Quality [IM] Senior Manager/Director of Commercial Quality for Johnson & Johnson in Japan, serving as the Japan Quality Leader. Responsible for ensuring post-marketing GxP activities comply with Japan GQP, J&J global quality policies, and MAH requirements. The role also fulfills legal responsibilities of Marketing Supervisor General under the PMD Act, overseeing market quality surveillance and regulatory compliance for pharmaceuticals and regenerative products. Key responsibilities include QMS governance, GxP compliance, market quality surveillance, MAH accountability, and cross-functional leadership. | — | 0 |
| Sr. Clinical Research Associate- Shockwave (Reducer) Johnson & Johnson is seeking a Sr. Clinical Research Associate to manage and execute global clinical studies for medical devices, ensuring compliance with regulatory standards. Responsibilities include study design, site management, data evaluation, and contract negotiation. | — | 0 |
| Senior QA Associate Senior QA Associate responsible for quality oversight and timely release of commercial API's, ensuring compliance with applicable regulations and providing quality support to production plants. | — | 0 |
| Commercial Quality Senior Executive This role is for a Commercial Quality Senior Executive at Johnson & Johnson in Malaysia. The position involves leading and implementing the Quality Management System (QMS) for operations in Malaysia & Brunei, overseeing critical processes like Change Control, Non-Conformance, CAPA, and Complaint Management. The role also requires managing quality oversight for labelling, packaging, and distribution, acting as a Subject Matter Expert (SME) for audits and inspections, and ensuring compliance with J&J standards and local regulations. Experience with digital tools like SAP, Power BI, and Power Automate is mentioned, but the core function is quality management in a regulated healthcare environment. | — | 0 |
| Manufacturing Tech III The Manufacturing Technician III role at Johnson & Johnson involves performing electro-mechanical assembly of robotic modules and components for surgical robotics. The position requires adherence to medical device regulations (ISO 13485, FDA QSR, GDP, GMP), operating within a structured production environment, conducting various tests, troubleshooting issues, and documenting production activities. The role also involves quality improvement initiatives, collaboration with engineering and quality teams, and training junior technicians. Experience with medical device manufacturing and a vocational certificate or associate degree is required. | — | 0 |
| [MedTech] Asso. Professional Education Manager - Electrophysiology The Associate Professional Education Manager for Electrophysiology & Neurovascular at Johnson & Johnson is responsible for developing and executing educational strategies and programs for healthcare professionals. This role involves collaborating with commercial teams, Key Opinion Leaders (KOLs), and cross-functional teams to ensure safe and effective product utilization, develop educational content, and ensure compliance with regulations. The position requires strong analytical, strategic thinking, and project management skills, with a focus on the Electrophysiology market. | — | 0 |
| Programa de Internship 2026 –Santiago de Chile (eic) Internship program at Johnson & Johnson focused on Sales and Marketing, supporting product launches, market research, and customer engagement strategies for pharmaceutical and MedTech products. | — | 0 |
| Sr. Manager, Tech., Insights & Analytics This role is for a Sr. Manager, Technology, Insights & Analytics at Johnson & Johnson, focusing on defining and owning the digital, data, and analytics strategy for global real estate, facilities management, and capital project delivery. The goal is to provide leadership with accurate insights for strategic decision-making, investment, portfolio optimization, and performance. Responsibilities include establishing a single source of truth for data, developing executive dashboards, incorporating external benchmarks, and leading a team of analytics professionals. The role requires a Bachelor's degree in a related field and 8-10 years of experience in analytics and business intelligence. | — | 0 |
| Sr. Manager, Process Engineering Sr. Manager, Process Engineering role at Johnson & Johnson (DePuy Synthes) focused on leading manufacturing and process engineering activities within a regulated medical device environment. Responsibilities include developing, optimizing, and sustaining robust manufacturing processes, driving continuous improvement, supporting new product introductions, and ensuring regulatory compliance. Requires a Bachelor's degree in Engineering and 8+ years of experience, including people leadership and experience in regulated manufacturing. | — | 0 |
| Clinical Research Leader, Neurovascular Johnson & Johnson MedTech, Neurovascular is seeking a Clinical Research Leader to lead and support clinical trials for neurovascular stroke treatments. Responsibilities include overseeing trial execution, site management, developing trial documents, ensuring regulatory compliance, data review, and collaborating with cross-functional teams. The role requires adherence to ICH-GCP and company SOPs. | — | 0 |
| Project Manager Engineering Project Manager, Engineering role at Johnson & Johnson (DePuy Synthes) responsible for planning, coordinating, and executing engineering projects supporting manufacturing operations, product development, and continuous improvement. This role requires managing cross-functional teams, ensuring project delivery on time and within scope, and compliance with quality and regulatory requirements in a regulated environment. | — | 0 |
| AM Engineering Projects This role is for an Automation Engineering Project Manager in the healthcare industry, focusing on the end-to-end execution of engineering, automation, and custom machine-building projects. Responsibilities include project management, vendor management, automation and controls expertise (PLC, HMI, SCADA, motion control), integration of vision systems, electrical and instrumentation engineering, and ensuring compliance with EHS, GMP, and validation requirements in a regulated environment. | — | 0 |
| Director Quality Assurance Director of Quality Assurance for Commercial Drug Product manufacturing, responsible for quality oversight, final release of Drug Products, and ensuring compliance with regulations. Acts as Qualified Person, overseeing GMP quality systems and leading a team of QA managers and professionals. | — | 0 |
| Operations Risk and Capacity Manager Operations Risk and Capacity Manager for DePuy Synthes, a Johnson & Johnson company, focused on managing strategic suppliers' risk and capacity health, planning for component flow and inventory, and orchestrating the Raw Material Strategic Capacity Program. The role involves assessing supplier capacity, identifying risks, and recommending actions to ensure production needs are met, particularly for new product introductions and lifecycle management. | — | 0 |
| Global Medical Affairs Leader Psoriatic Disease This role is for a Global Medical Affairs Leader in Psoriatic Disease at Johnson & Johnson, focusing on developing and leading global medical affairs strategies, clinical-commercial optimization, and lifecycle planning for specific assets. It involves collaboration with regional medical affairs, global publications strategy, KOL engagement, and representing medical affairs on various cross-functional teams. The role requires an advanced scientific or medical degree and at least 8 years of relevant experience in the pharmaceutical industry, with a strong preference for global medical affairs and dermatology therapeutic expertise. | — | 0 |
| Associate Director, Medical Science Liaison, Cardiac Electrophysiology for the Pacific Region Associate Director, Medical Science Liaison for Cardiac Electrophysiology in the Pacific Region. This role involves engaging with Key Opinion Leaders (KOLs), providing medical and scientific education, collaborating with internal teams, and staying updated on cardiac electrophysiology research and trends. The primary objective is to bridge the gap between J&J and customers by maintaining product knowledge and understanding scientific literature. | — | 0 |
| Sr. Princ. Process Engineer – DP Aseptic Biotherapeutic Filling Equipment Johnson & Johnson is seeking a Sr. Principal Process Engineer to lead end-to-end process engineering for aseptic drug product manufacturing, focusing on vial and syringe filling lines in a new cGMP facility. This role involves technical leadership in design, implementation, start-up, and optimization of filling systems, ensuring compliance with global regulatory expectations. | — | 0 |
| Sr. Principal Engineer, Aseptic DP Compounding Owner – Aseptic DP Compounding Sr. Principal Engineer, Aseptic DP Compounding Owner responsible for technical subject matter expertise in aseptic, biotherapeutic drug product compounding. This role leads the design, implementation, optimization, and compliance of compounding areas, including single-use technology, stainless steel tank design, mixing, and filtration. Responsibilities include developing specifications, assessing vendors, leading design and execution, commissioning, qualification, and issue resolution within a cGMP environment. | — | 0 |
| Senior Regulatory Affairs Specialist Senior Regulatory Affairs Specialist for J&J Vision products in Hong Kong and Macao, responsible for product registrations, renewals, lifecycle management, compliance, and supporting business activities. Requires experience with Hong Kong and Macao regulatory frameworks for medical devices. | — | 0 |
| Duales Studium Betriebswirtschaftslehre Duales Studium Betriebswirtschaftslehre (Business Administration) at Johnson & Johnson in Hamburg, Germany. This program offers a dual study path combining academic learning with practical experience in various business departments such as Sales, Marketing, HR, Controlling, and Product Management. The role focuses on general business administration, not AI/ML development. | — | 0 |