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 67 new AI-related roles. That is a -39% change versus the prior 30 days (109 → 67).
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 |
|---|---|---|
| Senior Director Site Engineering Lead Senior Director, Site Engineering Lead for BioTherapeutics and Lentivirus production at Johnson & Johnson in Leiden, Netherlands. This role oversees all engineering functions, manages a significant capital investment portfolio, and ensures the delivery of high-impact engineering projects and operational excellence. Responsibilities include developing and executing the Site Asset Master Plan, managing the capital project portfolio, directing the implementation of global automation strategy (ISA S95 Levels 0-1-2), defining and governing maintenance strategies, ensuring regulatory compliance, and driving the deployment of the Asset Management Framework. The role also involves cross-functional collaboration, stakeholder engagement, and providing executive oversight for digital tool implementation, including AI-enabled tools to drive productivity and efficiency. | — | 0 |
| LATAM Administration & Secretarial This role is an administrative and secretarial position within Johnson & Johnson, focusing on business support. It does not involve AI/ML development or research. | — |
| 0 |
| Business Analyst Business Analyst role at Johnson & Johnson (DePuy Synthes) in Seoul, Korea, focusing on data analytics and business intelligence. Responsibilities include communicating data findings, analyzing complex datasets for trends, establishing master data, and data visualization. Requires 3+ years of experience in business analysis/market intelligence, strong analytical skills, proficiency in SQL, Excel, and data visualization tools (Tableau/Power BI), and good communication skills in English and Korean. | — | 0 |
| Sr. Mgr, Prod/Pipe Comm Spine/Sports/CMF The Senior Manager, Product & Pipeline Communications is responsible for leading strategic communications for the Spine, Sports, and Craniomaxillofacial (CMF) portfolios within Johnson & Johnson's DePuy Synthes division. This role involves shaping how innovation, product strategy, and pipeline progress are communicated to internal and external audiences, supporting product launches, and ensuring communications are accurate, compliant, and aligned with business objectives and regulatory standards. The role requires strong collaboration with R&D, marketing, and corporate communications, as well as managing external agencies. | — | 0 |
| JJV PKG ENG 2027 CO-OP Co-op position for an aspiring package engineer in the healthcare industry, focusing on packaging design, validation, verification, procurement, and specification development for sterile and non-sterile products. Responsibilities include supporting project deliverables, understanding regulations (21 CFR, ISO standards), improving internal procedures, managing stakeholder relationships, and interacting with suppliers. Requires critical thinking and problem-solving skills. | — | 0 |
| Sr. Manager, Provincial Market Access The Sr. Manager, Provincial Market Access role at Johnson & Johnson is responsible for developing and executing market access strategies at the regional and provincial levels within China's healthcare system. This involves understanding and engaging with local healthcare policies, insurance, pricing, and procurement regulations, building relationships with authorities, and coordinating with internal teams to ensure compliant and effective market access for medical devices. | — | 0 |
| Senior Design Quality Engineer Senior Design Quality Engineer at Johnson & Johnson in Galway, Ireland, focusing on design control, risk management, and quality system compliance for new and existing medical products. Requires a degree in engineering, 5+ years of industry experience, and knowledge of medical device regulations (21 CFR 820, ISO 13485). | — | 0 |
| Director, Major Markets Europe & Canada Director of Regulatory Affairs for Major Markets Europe & Canada at Johnson & Johnson (DePuy Synthes). Responsible for leading regulatory strategy, ensuring compliance with EU, Canadian, and country-specific requirements, and enabling market access for medical devices. Partners with cross-functional teams, manages regulatory risk, and leads regional regulatory teams. | — | 0 |
| Director, Major Markets Europe & Canada Director of Regulatory Affairs for Major Markets Europe & Canada at Johnson & Johnson, focusing on ensuring compliance with local and regional regulatory requirements for medical devices and enabling market access. This role involves strategic leadership, cross-functional partnership, and team management within a highly regulated environment. | — | 0 |
| Director, Major Markets Europe & Canada Director of Regulatory Affairs for Major Markets Europe & Canada at Johnson & Johnson (DePuy Synthes). This role focuses on ensuring compliance with regulatory requirements for medical devices, managing product registrations, renewals, and lifecycle management, and partnering with cross-functional teams to enable market access and business growth in highly regulated markets. The position requires strong leadership and strategic guidance in regulatory affairs within the healthcare industry. | — | 0 |
| Director, GDCL oUS (North & South Asia) Director, Global Deliver & Customer Logistics (GDCL) oUS for Southeast & North Asia (SENA) within DePuy Synthes Orthopedics. Responsible for overseeing and advancing GDCL strategy, end-to-end customer logistics, distribution, and delivery operations, ensuring service, cost, quality, and compliance. Drives continuous improvement, digital enablement, and operational excellence. Requires 12-15 years of progressive experience in supply chain/logistics/operations leadership in a regulated industry. | — | 0 |
| IT Director Architecture EMEA IT Director Architecture EMEA at Johnson & Johnson responsible for shaping the end-to-end application architecture strategy, enabling secure integration, reusability, and faster delivery of business value. The role involves setting the EMEA architecture direction across technology, business process, data, AI, security, and solution design, influencing product roadmaps, championing reusable platforms and patterns, and partnering across product, engineering, and global architecture. | — | 0 |
| Job Posting Title Associate Director, QARA SE Asia & India Associate Director, Quality Assurance & Regulatory Affairs (QARA) – Southeast Asia & India, providing regional leadership for quality assurance and regulatory affairs, ensuring regulatory compliance, effective quality management system execution, and sustainable market access across diverse and highly regulated markets in the healthcare industry. | — | 0 |
| Director, RA Submissions CTA Director, RA Submissions CTA at Johnson & Johnson, responsible for end-to-end stewardship of Clinical Trial Application (CTA) submission delivery globally, with a focus on EU compliance under the EU CTR. The role involves setting strategic direction, defining operating models and standards, driving continuous improvement, and leading a team of professionals. Key responsibilities include ensuring high-quality, compliant submissions, managing capacity, assessing and adapting capabilities, and acting as a subject matter authority. | — | 0 |
| Manager, Strategic Planning Manager, Strategic Planning for DePuy Synthes China, focusing on shaping portfolio strategy, ecosystem partnerships, and data-enabled decision making to drive growth. Responsibilities include market analysis, initiative governance, market intelligence, data catalog management, and analytics governance. | — | 0 |
| Director, Quality Assurance, Regulatory Affairs, Distribution and Operations, APAC Director, Quality Assurance, Regulatory Affairs, Distribution and Operations, APAC for Johnson & Johnson's DePuy Synthes in Pune, India. This role provides enterprise-level leadership for quality assurance and regulatory affairs across the Asia-Pacific region, ensuring local market regulatory compliance, quality management system execution, and sustainable market access. The position is a key member of the international QARA leadership team and partners closely with Global QARA, Commercial, Operations, and Supply Chain leaders, impacting patient safety, compliance outcomes, and the long-term success of the APAC portfolio in highly regulated markets. | — | 0 |
| Senior Manager - Supply Chain Procurement, PMO Senior Manager role focused on program management for continuous improvement initiatives within supply chain procurement for Johnson & Johnson's MedTech Surgery Business Unit. The role involves optimizing direct material costs, deploying value creation strategies, managing end-to-end portfolios, and driving process harmonization and digitization. | — | 0 |
| Associate Director, Audit Process Lead The Associate Director, Audit Process Lead will be the global, cross-domain Audit Business Process Owner (BPO) for R&D Quality (RDQ), with end-to-end accountability for the RDQ audit process across people, process, and technology. This role will set the strategic direction for the audit process, lead continuous improvement efforts, and ensure the process remains efficient, effective, compliant, and aligned with evolving regulatory expectations and industry leading practices. This role will also expand and strengthen RDQ’s partnership with other audit-related functions within J&J, as well as external organizations, to establish a sustainable approach to innovation and audit process modernization. | — | 0 |
| Sr Manager, Business Analytics & Ops This role is a Sr. Manager for Business Analytics & Operations at Johnson & Johnson's DePuy Synthes division in Shanghai. The primary focus is on driving data-driven decision-making, ensuring operational efficiency, and maintaining office governance. Responsibilities include developing analytics frameworks, overseeing sales operations processes (sample management, tendering, etc.), ensuring compliance with company policies and audits, translating business needs into requirements for IT/Digital, supporting data governance, managing office operations, and leading a team. The role acts as a central hub connecting various departments like Sales, Marketing, Finance, IS, and HR. | — | 0 |
| Quality Speicialist-QS&CQ Quality Specialist role at Johnson & Johnson in Suzhou, China, focusing on quality management systems, complaint handling, post-market surveillance, and risk management for medical devices. The role involves collaborating with cross-functional teams, analyzing data using statistical techniques, supporting factory projects, and ensuring compliance with regulations like ISO13485 and GMP. | — | 0 |
| Director, Major Markets Europe & Canada Director of Regulatory Affairs for Major Markets in Europe and Canada, responsible for strategic regulatory leadership, ensuring compliance with EU, Canadian, and country-specific requirements, and enabling market access for medical devices. This role involves partnering with cross-functional teams, managing regulatory risk, and leading regional regulatory teams. | — | 0 |
| Supervisor Grondstoffentankpark Supervisor role responsible for the operational management of a raw material tank farm (bulk solvents) at a Johnson & Johnson facility. This includes managing a team of operators, overseeing processes like unloading and sampling, ensuring quality and compliance, and driving continuous improvement initiatives. | — | 0 |
| Technical Product Owner - ERP Master Data Johnson & Johnson is seeking a Technical Product Owner for their ERP Master Data Governance program. The role involves translating business requirements into technical deliverables, managing the Agile backlog, overseeing development and testing, and ensuring compliance with data governance principles. This is a product management role focused on master data within an ERP system. | — | 0 |
| Crystallographer, Experienced Scientist R&D This role focuses on crystallography and solid-state chemistry to characterize and control polymorphism of active pharmaceutical ingredients (APIs) for drug development. It involves applying expertise in X-ray, electron, or neutron diffraction techniques for structure determination and analysis, collaborating with cross-functional teams, and ensuring compliance with laboratory standards. The role requires a PhD in a related field and experience in solid-state materials science. | — | 0 |
| Sr. Manager, Central GA Strategy The Sr. Manager, Central GA Strategy role at Johnson & Johnson (DePuy Synthes) in Shanghai, China, is responsible for central-level government policy intelligence, strategic analysis, and engagement strategy. This role involves independent research and interpretation of central healthcare and economic policies, translating them into actionable business and access strategies, and advising leadership. Key responsibilities include tracking and assessing policy impacts, developing central GA and market access strategies, supporting high-level government engagement, building external ecosystem intelligence, and providing internal enablement and strategic coordination. | — | 0 |
| Principal Scientist, Extractables & Leachables (E&L) The Principal Scientist, Extractables & Leachables (E&L) role at Johnson & Johnson focuses on providing technical expertise in E&L studies for closure container systems and drug-device combination products. The role involves designing, executing, and evaluating these studies, interpreting complex analytical data (LC-MS, GC-MS), and ensuring alignment with global regulatory expectations. The scientist will also manage contract laboratories and contribute to regulatory documentation and responses. This is a research-focused role within the healthcare domain, requiring deep scientific judgment and experience with analytical chemistry and regulatory compliance. | — | 0 |
| Manager External Quality Advanced Therapies Manager External Quality for Advanced Therapies at Johnson & Johnson, focusing on quality assurance for apheresis material collection and cell cryopreservation for CAR-T products. Responsibilities include auditing external partners, providing quality oversight, monitoring trends, and ensuring compliance with health authority requirements and cGMP/GTP standards. | — | 0 |
| Manager, Regulatory Affairs - Spain Manager, Regulatory Affairs for Spain and Portugal at Johnson & Johnson's DePuy Synthes (orthopaedics business). Responsible for leading regulatory affairs activities, ensuring compliance with local and regional requirements, supporting product registrations, renewals, and lifecycle management to enable timely market access and business continuity. Partners with cross-functional teams and monitors regulatory changes. | — | 0 |
| Associate Director, Audit Process Lead The Associate Director, Audit Process Lead is responsible for the global, cross-domain Audit Business Process Owner (BPO) for R&D Quality (RDQ), with end-to-end accountability for the RDQ audit process. This role will set the strategic direction, lead continuous improvement, and ensure the process is efficient, effective, compliant, and aligned with evolving regulatory expectations and industry leading practices. The role also involves expanding partnerships, exploring digital enablers, and managing change for audit process updates. | — | 0 |
| Director, MedTech Technology Surgery Product Group Leader, APAC Director, MedTech Technology Surgery Product Group Leader, APAC for Johnson & Johnson. This role sets the vision, strategy, and objectives for a product group, focusing on commercial excellence, customer engagement, sales force productivity, and education outcomes in the Asia Pacific region. The leader will work closely with the Butterfly team for flawless implementation. Responsibilities include defining product group vision, orchestrating cross-product roadmaps, managing stakeholder partnerships, tracking metrics for value realization, financial stewardship, and fostering a culture of empowerment and agile practices. | — | 0 |
| Director, RE Delivery - EMEA/APAC This role is for a Director of Real Estate Delivery for EMEA/APAC at Johnson & Johnson, focusing on executing real estate transactions, projects, and portfolio initiatives. It involves leading regional delivery teams, ensuring compliance with local regulations, and aligning the real estate portfolio with business needs. The role requires managing leases, renewals, exits, and overseeing project execution to meet scope, cost, schedule, and quality standards. | — | 0 |
| Marketing Intern, Surgical Vision This is a Marketing Intern position at Johnson & Johnson, supporting the Surgical Vision Sales team. The role involves providing logistical and administrative support to marketing projects, executing administrative and clerical marketing assignments, processing purchase orders, coordinating marketing functions, assisting in the creation of sales tools and programs, and ensuring marketing materials are approved and updated. The ideal candidate is pursuing a Diploma or Bachelor's degree, has excellent communication skills, is proficient in Microsoft Office, and demonstrates strong learning agility. | — | 0 |
| Sr. Manager, Provincial Market Access The Sr. Manager, Provincial Market Access role at Johnson & Johnson (DePuy Synthes) in China is responsible for developing and executing regional/provincial market access strategies, engaging with authorities, and managing reimbursement policies for medical devices. This involves understanding local healthcare, insurance, pricing, and procurement policies, building relationships with government bodies, and aligning strategies with business objectives. | — | 0 |
| Sr Design Quality Engineer Sr Design Quality Engineer at Johnson & Johnson in Shanghai, China, focusing on the entire product life cycle with activities in reliability, risk management, analytics, requirements management, verification & validation, and design control. The role involves applying Six Sigma and Lean methodologies, ensuring conformance to quality systems (ISO, FDA, MDR), and acting as a technical liaison. Requires strong analytical and statistical problem-solving skills. | — | 0 |
| Education Solution Specialist (m/f/d) The Education Solution Specialist supports the planning, coordination, execution, and analysis of Professional Medical Education (PME) programs for DePuy Synthes. This role ensures operational excellence, compliance, and data transparency across educational activities and acts as a key interface between Professional Education, commercial teams, and external stakeholders. Responsibilities include program support, data analysis, compliance, stakeholder coordination, and process improvement. | — | 0 |
| Director, QARA European MSM & CEE Director, QARA European MSM & CEE role at Johnson & Johnson, responsible for Quality Assurance and Regulatory Affairs across European markets. Ensures regulatory compliance, quality system execution, and market access, partnering with various teams and leading regional QARA leaders. Requires strong knowledge of EU MDR and European regulatory frameworks. | — | 0 |
| Quality Speicialist Quality Specialist role at Johnson & Johnson in Suzhou, China, focusing on quality management systems, complaint handling, post-market surveillance, and risk management for medical devices. Responsibilities include data analysis, process improvement, supporting factory projects, and ensuring compliance with regulations like ISO13485 and GMP. | — | 0 |
| Country Manager Kenya Country Manager for Johnson & Johnson in Kenya, responsible for delivering business results and driving growth through sales, innovation, and distributor management. The role involves strategic planning, team leadership, compliance with local and international regulations, and stakeholder relationship management within the healthcare sector. | — | 0 |
| Manager, Clinical Research Manager, Clinical Research role at Johnson & Johnson, focusing on leading clinical study operations for the orthopedic portfolio. Responsibilities include study planning, execution, site selection, ensuring regulatory compliance (GCP), stakeholder management, and supporting audits. Requires a Bachelor's degree with 6-8 years of clinical research experience. | — | 0 |
| Sr. Manager, QARA China Ops & Dist. This role is for a Sr. Manager, QARA China Ops & Dist. at Johnson & Johnson (DePuy Synthes) in Shanghai, China. The position focuses on providing senior operational leadership for quality assurance and regulatory affairs, ensuring compliance with China regulatory requirements, managing quality systems, and supporting compliant business growth within operations and distribution. It requires strong knowledge of regulated industries, China regulations, and cross-functional collaboration. | — | 0 |
| 皮科市场部实习生 This is an internship position in the marketing department at Johnson & Johnson, focusing on assisting with market promotion activities, data analysis, and communication. The role requires proficiency in office software and good communication skills. | — | 0 |
| Manager, APAC, Regulatory Affairs, Immunology Manager, Regulatory Affairs for the APAC region at Johnson & Johnson, responsible for defining and implementing regional strategies for product registration and lifecycle management, providing regulatory support to local affiliates, and managing interactions with Health Authorities and operating companies. | — | 0 |
| Loan Kits Team Leader Team Leader for a Loan Kit warehouse team at Johnson & Johnson, focusing on managing daily operations, staff development, process improvement, and issue resolution within a supply chain manufacturing environment. | — | 0 |
| Manager, QARA Hong Kong Manager, QARA Hong Kong provides operational leadership for quality assurance and regulatory affairs supporting the Hong Kong market for DePuy Synthes’ Orthopedics portfolio. This role ensures regulatory compliance, effective quality management system execution, and sustained market access in a highly regulated environment. | — | 0 |
| MSL-Neuro Medical Science Liaison (MSL) role focused on engaging Key Opinion Leaders (KOLs) in a specific therapeutic area to provide scientific support for research, publications, and education. The role involves communicating medical and scientific data, collecting insights, organizing medical education activities, and identifying evidence gaps to support therapeutic area strategy. Requires a strong understanding of the therapeutic area and excellent communication and analytical skills. | — | 0 |
| Loan Kit Technician This role is a Loan Kit Technician in the MedTech Orthopaedics team at Johnson & Johnson. The primary responsibilities include inspecting, assembling, managing the dispatch and receipt of orthopaedic loan sets, and ensuring their cleanliness and functionality. The role also involves inventory management, liaising with hospitals, and collaborating with internal teams to meet customer requirements. It requires attention to detail, efficiency in a fast-paced environment, and strong problem-solving and communication skills. Adherence to quality standards and policies like ISO 13485 is critical. | — | 0 |
| Professional Relations & Operations Specialist - Sydney This role is responsible for the strategic and compliant management of Education Grants, Fellowships, Donations and Fee-for-Service payments within the Surgery business unit, ensuring financial management aligns with organizational objectives and enhancing educational initiatives in the ANZ region. It involves managing external stakeholders, processing payments, and analyzing financial data. | — | 0 |
| HSD Specialist This role supports Health, Safety, and Distribution (HSD)-related quality activities for commercial operations in Japan, ensuring compliance with regulatory requirements, quality system standards, and internal procedures. It involves supporting distribution, handling, and post-market activities, partnering with various teams, and monitoring quality issues. | — | 0 |
| Health Care Compliance Intern This is an internship role focused on assisting with the daily operations of a compliance program within Johnson & Johnson's healthcare sector. Responsibilities include data collection, information sorting, document filing, process follow-up, and supporting the creation and optimization of training and communication materials. The role also involves providing support for ad hoc compliance projects. | — | 0 |
| Director, Quality Assurance, Regulatory Affairs, Distribution and Operations, APAC Director, Quality Assurance, Regulatory Affairs, Distribution and Operations, APAC for Johnson & Johnson's DePuy Synthes within the healthcare domain. This role focuses on leading regional QARA strategy, ensuring compliance with regulatory requirements and quality management systems, and managing health authority interactions across the Asia-Pacific region. It involves executive oversight of submissions, approvals, and lifecycle management, partnering with various business functions, and leading regional QARA teams. | — | 0 |