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 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).
| Title | Stage | AI score |
|---|---|---|
| LOC Sr Reg Compliance Specialist This role is for a Senior Regulatory Compliance Specialist at Johnson & Johnson in Singapore. The primary focus is on leading and executing regulatory compliance activities for the local operating company, ensuring adherence to regulations, quality systems, and internal policies for commercial and distribution activities. Responsibilities include supporting internal and external audits, monitoring compliance risks, and maintaining documentation. The role requires a Bachelor's degree and 4-6 years of experience in a regulated industry, with a strong knowledge of local commercial operation compliance requirements. | — | 0 |
| Sr. Director, GDCL oUS Lead (Japan) Sr. Director, Global Deliver & Customer Logistics (GDCL) oUS Lead for Japan within DePuy Syntheshes Orthopedics. Responsible for overseeing and advancing GDCL strategy, ensuring compliant, efficient, and patient-focused supply chain operations, and leading transformation initiatives. Requires 12-15 years of experience in supply chain/logistics/operations leadership in a regulated industry, with strong knowledge of end-to-end supply chain processes. Fluent Japanese and English required. |
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| Sales & Marketing Coordinator Sales & Marketing Coordinator at Johnson & Johnson (DePuy Synthes) to provide administrative assistance to commercial teams, coordinate demo equipment and sales collaterals, process invoices, manage events, and support sales/marketing tools. | — | 0 |
| Staff Process Engineering Staff Process Engineer role focused on leading projects, process improvement, and characterization activities for manufacturing processes in the healthcare industry. Responsibilities include problem identification, root cause analysis, project management, and driving continuous improvement within a GMP/ISO compliance framework. Requires strong analytical and problem-solving skills, experience with statistical tools, and collaboration within multi-functional teams. | — | 0 |
| Senior Sustaining Engineer Senior Sustaining Engineer responsible for lifecycle support of commercially released medical instruments and capital equipment for the MONARCH Platform. This role involves leading failure investigations, driving design and process improvements, managing component obsolescence, and ensuring product safety, performance, and regulatory compliance within a regulated medical device environment. | — | 0 |
| Business Products Owner, Business Development This role is for a Business Products Owner focused on Business Development technology assets, including the "BD Intelligence Command Center". The responsibilities include product strategy, delivery, operations, governance, and continuous improvement of these technologies to support deal flow and decision-making. The role requires experience in product management, cloud architecture, APIs, BI tools, CRM platforms, and Agile practices. Experience in regulated environments is preferred. | — | 0 |
| Senior Manager, OTTAVA Communications Senior Manager, OTTAVA Communications for Johnson & Johnson MedTech's Surgery business, responsible for creating strategic communications programs for surgical robotics and digital surgery. This role involves employee and culture communications, executive communications, strategic messaging, thought leadership, media relations, social media, and campaign activations, working closely with R&D, clinical, medical, and business teams. | — | 0 |
| Senior Principal Mechanical Engineer (HTI) - JJMT Electrophysiology The Senior Principal Mechanical Engineer role is focused on leading the incubation of early-stage catheter innovations within the Haifa Tech Incubator (HTI) for Johnson & Johnson MedTech Electrophysiology. This role involves driving the development of novel catheter designs from concept to prototype, integrating advanced materials and navigation technologies, and ensuring alignment with clinical needs and regulatory pathways. The engineer will collaborate with cross-functional teams and external partners to bring disruptive technologies to market, aiming to improve patient outcomes in cardiovascular care. | — | 0 |
| Director, Communications - Advanced Surgical Instruments Director of Communications for Advanced Surgical Instruments at Johnson & Johnson, focusing on strategic communications, thought leadership, media strategy, content development, and campaign activations to drive business outcomes in the healthcare and MedTech sectors. Requires experience in healthcare, MedTech, or robotics, and strong writing and collaboration skills. | — | 0 |
| Senior Manager Category Procurement IM MOPS This role is responsible for leading the Marketing Operations (MOPS) Procurement category of spend for the Innovative Medicine sector, managing approximately $250MM in external supplier spend. The responsibilities include developing and implementing end-to-end procurement strategies, managing supplier partnerships, leading global strategic negotiations, and collaborating with various internal teams to ensure alignment with business strategies. | — | 0 |
| PRINCIPAL QUALITY TECHNICIAN Principal Quality Technician at Johnson & Johnson MedTech, responsible for quality control, training associates, investigating non-conformities, performing product release activities, customer complaint analysis, data collection and reporting, and maintaining quality records and systems. Requires experience in quality control and knowledge of quality engineering tools. | — | 0 |
| Associate Vein-to-Vein Planner CAR-T Associate Vein-to-Vein Planner for CAR-T therapy at Johnson & Johnson, focusing on supply chain planning, demand actualization, and managing the patient journey from enrollment to infusion. Responsibilities include data analysis, logistics support, and collaboration with various internal and external teams to ensure timely treatment delivery. | — | 0 |
| Senior Manager Category Procurement IM MOPS Senior Manager Category Procurement IM MOPS for Johnson & Johnson's Innovative Medicine sector, responsible for managing approximately $250MM in external supplier spend. The role involves developing and implementing end-to-end procurement strategies, managing supplier relationships, leading global negotiations, and collaborating with various internal teams to ensure alignment with business strategies and operational efficiency. | — | 0 |
| Cybersecurity Lead MedTech R&D Johnson & Johnson is seeking a Cybersecurity Lead for their MedTech R&D division. This role involves partnering with technology and business teams to ensure the secure development and implementation of innovative technology solutions, protect intellectual property, and drive cybersecurity adoption across R&D labs. The lead will provide security guidance, manage security assessments and remediation, and ensure compliance with cybersecurity regulations. | — | 0 |
| Automation Engineer II Automation Engineer II at Johnson & Johnson MedTech responsible for design, installation, and qualification of new manufacturing equipment and improvement/optimization of existing manufacturing equipment. Provides technical expertise to resolve manufacturing equipment and automation issues. Collaborates with other plant functions and external vendors, manages projects, supports qualification, leads/supports investigations, evaluates new technologies, prepares reports, coordinates training, analyzes maintenance trends, and ensures compliance with regulations. | — | 0 |
| SENIOR ENGINEERING TECHNICIAN This role is for a Senior Engineering Technician in Supply Chain Manufacturing, focusing on Production Equipment Repair & Maintenance. Responsibilities include supporting engineers, operating and maintaining manufacturing equipment, performing diagnostics and repairs, ensuring calibration of tools, and supporting installation and validation processes. The role requires knowledge of electronics, mechanics, or related fields, and experience with maintenance, calibration, and quality systems. | — | 0 |
| Senior Quality Enigneer Senior Quality Engineer at Johnson & Johnson in Ciudad Juarez, Mexico, responsible for leading quality improvement efforts, developing quality control and risk management plans, writing validation protocols, analyzing data using statistical tools, determining test requirements for new products, supporting vendor audits, initiating CAPAs, assisting in complaint analysis, supporting regulatory submissions, and participating in design reviews. Requires a Bachelor's degree in a related field with 4-6 years of experience in a regulated industry. | — | 0 |
| Preclinical Research Intern - (Irvine, CA) Johnson and Johnson MedTech, Electrophysiology This is an internship role focused on preclinical research in Electrophysiology within Johnson & Johnson MedTech. The intern will support scientists and data engineers in applying preclinical data to drive clinical success, gather data from various sources, assist in planning research methodology, and analyze data to identify trends and discrepancies in patient outcomes. The role involves working with clinical studies, post-marketing studies, and Real World Evidence registry studies. | — | 0 |
| Senior Hematology Medical Science Liaison - Rio de Janeiro Senior Hematology Medical Science Liaison role at Johnson & Johnson based in Rio de Janeiro. The role involves engaging with healthcare professionals (HCPs) to discuss treatments, share scientific knowledge, gather medical insights, and support medical strategy. Key activities include building relationships with HCPs, conveying product attributes, executing educational events, shaping medical practice, designing KOL engagement plans, and responding to scientific inquiries. Requires a Master's degree, deep therapeutic area knowledge, previous MSL experience, and proficiency in English. | — | 0 |
| Medical Affairs Director – Hematology The Medical Affairs Director – Hematology is responsible for medical and scientific leadership of the J&J Hematology Therapeutic Area strategy, spanning hematological malignancies including multiple myeloma, lymphoid, and myeloid malignancies, across in-line and pipeline assets. The role provides evidence-based scientific expertise to internal and external stakeholders and is accountable for the Integrated Evidence Generation Process (IEGP) in close collaboration with the Therapeutic Area team and global partners. This role has three direct reports and requires deep experience in hematological malignancies, people leadership, and knowledge of GCP, IMC Code, compliance, and Canadian regulatory requirements. | — | 0 |
| Operations Specialist Operations Specialist at Johnson & Johnson in Anasco, Puerto Rico, responsible for managing non-conformances (NRs), corrective and preventive actions (CAPAs), and audit observations within a manufacturing engineering context. Requires experience with regulatory compliance, root cause analysis, and problem-solving methodologies in a regulated medical device environment. | — | 0 |
| Oncology Clinical Educator, Solid Tumors (Upstate NY & CT) This role is for an Oncology Clinical Educator at Johnson & Johnson, focusing on providing clinical education for Innovative Medicine Oncology brands to non-physician patient care teams (PCTs) and patients. The educator will build relationships, develop strategic territory plans, and educate on disease states, product profiles, and administration. The role requires understanding clinical and administrative aspects of new cancer medications and ensuring all activities comply with regulatory and healthcare guidelines. | — | 0 |
| Spec Tech Prod Equip Repair This role is responsible for maintaining and repairing manufacturing equipment within the J&J MedTech Orthopedics division, ensuring maximum asset availability and reliability. It involves preventive and predictive maintenance, troubleshooting, and record-keeping using a CMMS. | — | 0 |
| Associate Director, HEMA, Surgical Robotics Associate Director, Health Economics & Market Access (HEMA) for Surgical Robotics, focusing on the OTTAVA Platform. This role involves identifying evidence gaps, executing economic studies, demonstrating clinical/operational/economic value, and creating customer-facing materials to support adoption. | — | 0 |
| Medical Scientific Liaison - Costa Rica Johnson & Johnson is seeking a Medical Scientific Liaison in Costa Rica to engage with healthcare professionals, share scientific information, support clinical programs, and gather competitive intelligence. The role involves developing and implementing medical affairs plans, providing scientific expertise, and ensuring compliance with regulations. | — | 0 |
| Director, Transcend-PLAN BPL Johnson & Johnson is seeking a senior leader for their Supply Chain Planning function to oversee global business processes within the Transcend program. This role involves defining process standards, managing capability roadmaps, and aligning teams to deliver business value. The position requires extensive experience in supply chain planning, business process design, and SAP ERP implementations, with a focus on driving operational readiness and continuous improvement. | — | 0 |
| Senior Analyst, PMO Surgery This role is a Senior Analyst within the PMO Surgery team at Johnson & Johnson, supporting large-scale business and technology transformation initiatives. The primary focus is on project management activities, including planning, risk management, change management, and facilitating stage-gate reviews. The role involves data analysis, reporting, and serving as a subject matter expert on project management tools. | — | 0 |
| Director, Transcend-PLAN BPL Johnson & Johnson is seeking a Director, Transcend-PLAN BPL to lead global Supply Chain Planning processes within their large-scale business transformation initiative. This role involves driving process standards, capability roadmaps, and ensuring operational readiness and compliance for SAP S/4 HANA implementations. The position requires extensive experience in supply chain planning, business process design, and cross-functional leadership. | — | 0 |
| Master Scheduler The Master Scheduler role at Johnson & Johnson is responsible for developing and maintaining a constrained Master Production Schedule (MPS) that aligns site capacity with network requirements. This role involves site capacity planning, leading Rough-Cut Capacity Planning (RCCP) reviews, managing the Latest Estimate (LE) process, and collaborating with global teams to mitigate constraints. The position utilizes advanced planning systems for scenario modeling and predictive analytics, partners with data analytics teams to leverage AI/ML-based forecasting, and drives continuous improvement and digital transformation within planning processes. It also involves risk management, ensuring compliance with regulatory standards, and coordinating production requirements and inventory management. | — | 0 |
| DOCUMENT CONTROL CHANGE ANALYST II (TEMPORARY 12 MONTHS) The Document Control Change Analyst II role at Johnson & Johnson is responsible for managing and analyzing documentation changes within a supply chain manufacturing environment. This includes reviewing change requests, ensuring accuracy and consistency, proofreading documents, and providing guidance on change control processes. The role also involves supporting quality systems, audits, and records management. | — | 0 |
| Senior Quality Engineer – Orthopedics Senior Quality Engineer for Orthopedics at Johnson & Johnson, focusing on quality assurance leadership for contract manufacturing sites, conducting audits, and ensuring compliance with global regulations and standards (QSRs, ISO 13485, etc.). The role involves supporting quality improvement initiatives, new product introductions, non-conformance investigations, and validation strategies within the regulated medical device industry. | — | 0 |
| Process Engineer (Machining), Orthopedics Process Engineer role focused on maintaining and improving manufacturing processes for orthopedic products, including CNC programming, process optimization using PE principles, and ensuring quality and compliance with FDA and ISO standards. | — | 0 |
| Internship Organic & Medicinal Chemistry Internship role in Organic & Medicinal Chemistry at Johnson & Johnson's Innovative Medicine division in Toledo, Spain. Focuses on the design, synthesis, and optimization of small molecule therapeutics, contributing to drug discovery projects using advanced synthetic chemistry techniques. | — | 0 |
| Embedded Software Engineer Embedded Software Engineer role at Johnson & Johnson focused on developing software for medical devices, adhering to strict development lifecycles and collaborating with cross-functional teams. Requires strong C/C++ skills on embedded platforms and experience with real-time operating systems. | — | 0 |
| MT Shared Doc and RIC Admin The MT Shared Documents and Records & Information Compliance (RIC) Administrator role at Johnson & Johnson focuses on implementing and managing document and change control processes for MedTech Shared Documents using PLM systems like Windchill. The role involves providing guidance to internal customers, processing changes, collecting metrics, leading projects for departmental objectives, supporting audits and quality events, and ensuring adherence to quality systems and regulatory requirements. A key responsibility is supporting and recommending process improvements, including exploring automated solutions like PowerApps. Experience in regulated industries and with Windchill change control systems is required, with a preference for experience with machine learning and AI. | — | 0 |
| Senior Engineer, Primary Container, Biologics The Senior Engineer, Primary Container, Biologics, will lead the development, selection, qualification, and lifecycle management of vial systems, pre-filled syringes, cartridges, and emerging container technologies for new biologic drug products. The role ensures all primary containers comply with global regulatory, technical, and quality standards while driving innovation and operational excellence. | — | 0 |
| Senior Medical Science Liaison-Neuroimmunology-Southern California This role is for a Senior Medical Science Liaison in Neuroimmunology at Johnson & Johnson. The primary responsibilities include providing scientific and clinical information to healthcare professionals and opinion leaders, developing territory strategic plans, and supporting research. The role requires strong knowledge of the therapeutic area, relationship-building skills, and adherence to compliance guidelines. It involves significant travel and requires a PharmD, PhD, MD, NP, or PA with relevant experience. | — | 0 |
| Medical Science Liaison - Hematology/Oncology (Oregon/Idaho) This role is for a Medical Science Liaison in Hematology/Oncology for Johnson & Johnson Innovative Medicine. The MSL will act as a field-based scientific and clinical expert, developing relationships with Key Opinion Leaders (KOLs) and healthcare professionals (HCPs). Responsibilities include providing scientific information, engaging in scientific exchange, identifying unmet needs, and supporting investigator-initiated studies. The role also involves leveraging AI tools to improve decision-making and efficiency, staying updated on the therapeutic area, and collaborating with internal stakeholders. A strong understanding of regulatory and healthcare compliance is required. | — | 0 |
| Utility Operator/Mechanic III Experienced Operating Engineer responsible for the operation and maintenance of utility systems in a biologics pharmaceutical manufacturing environment. This role involves corrective, emergency, and preventive maintenance on equipment such as boilers, chillers, cooling towers, and clean-in-place systems, ensuring compliance with all regulations and guidelines. Requires a strong understanding of industrial maintenance and the ability to respond to off-shift issues. | — | 0 |
| Quality Assurance - delegate QP Quality Assurance Associate for CAR-T hub in Europe, responsible for ensuring manufacturing processes meet quality standards and regulatory requirements, including batch review and release, investigations, deviations, complaints, CAPA management, and audit support. Requires a degree in Pharmacy or Bio-engineering and certification as an Industrial Pharmacist (Qualified Person). | — | 0 |
| Staff Mechanical Engineer, R&D Staff Mechanical Engineer, R&D role at Johnson & Johnson supporting the development of electrophysiology catheters and systems. Responsibilities include design, requirement development, design for manufacturing, design transfer, test method development, and product verification/validation testing. Requires a Bachelor's degree in Mechanical or Biomedical Engineering with significant experience and leadership in medical device development. | — | 0 |
| [Innovative Medicine] Clinical Research Associate Entry-level Clinical Research Associate (Associate Site Manager) role at Johnson & Johnson's Innovative Medicine division. Responsible for managing investigational trial sites, ensuring compliance with protocols, SOPs, GCP, and regulations. Duties include assisting with site selection, recruitment, monitoring, and close-out activities, acting as the primary contact between the sponsor and the site. | — | 0 |
| Technical Regulatory Associate Johnson & Johnson is seeking a Technical Regulatory Associate in Latina, Italy, to join their Quality Systems department. The role focuses on ensuring product compliance with national and international pharmaceutical regulations, managing change control processes, and preparing registration documentation. This position requires a Master's degree in a relevant scientific field, 1-3 years of experience in Quality Assurance within regulated environments, and knowledge of GMP. | — | 0 |
| Sr Healthcare Solutions Business Analyst This role focuses on designing, developing, and maintaining Tableau dashboards to track KPIs and produce actionable insights for Healthcare Solutions teams. It involves establishing KPI definitions, dashboard governance, and data quality checks, as well as cross-functional alignment with IT and Commercial functions. The analyst will partner with the CRM team to improve business processes and translate business questions into analytics requirements, performing ad-hoc analyses and presenting findings to stakeholders. The role also includes providing training, documentation, and support for leadership with business reviews and data storytelling, while ensuring compliance with data privacy and security policies. | — | 0 |
| Sr. QA Associate - Commercial Synthetics Senior QA Associate for Commercial Synthetics at Johnson & Johnson, focusing on quality oversight and timely release of commercial Active Pharmaceutical Ingredients (APIs). Responsibilities include ensuring compliance with regulations, supporting production plants, managing non-conformances and CAPAs, reviewing quality reports, and acting as a Subject Matter Expert during inspections. Requires a Master's degree in a scientific field and strong knowledge of cGMP and Quality Systems. | — | 0 |
| Business Unit Lead Lung (m/w/d) This role is for a Business Unit Lead for the Lung oncology portfolio at Johnson & Johnson. The primary focus is on accelerating growth, maximizing portfolio potential, and driving launch excellence in a competitive market. The role involves P&L accountability, strategic leadership, cross-functional orchestration, and leveraging digital innovation and AI to enhance decision-making and execution. The ideal candidate will have strong leadership experience in oncology, a proven track record in driving growth, and the ability to leverage digital tools, analytics, and AI for business performance. | — | 0 |
| Site Manager / CRA The Site Manager / CRA role at Johnson & Johnson focuses on managing clinical trial sites, acting as the sponsor's interface with investigative sites, and overseeing all aspects of site management from pre-trial assessments to close-out activities. This role is within R&D Operations, specifically Clinical Trial Support, and requires strong communication, problem-solving, and knowledge of GCP and regulatory guidelines. The company is a leader in healthcare innovation, particularly in drug development across various therapeutic areas. | — | 0 |
| Senior Compliance Lead This role is for a Senior Compliance Lead at Johnson & Johnson, focusing on managing internal audit programs and external GMP inspections for the Geel site. The position requires expertise in pharmaceutical regulatory compliance, coordinating compliance personnel, and ensuring site inspection readiness. It involves identifying regulatory changes, providing compliance subject matter expertise, and facilitating remediation of compliance risks. | — | 0 |
| Sr Director, C&SP - NS and Cardio-Pulmonary Senior Director role in Clinical & Statistical Programming (C&SP) at Johnson & Johnson Innovative Medicine, focusing on Neuroscience & Cardio-Pulmonary. The role involves strategic leadership, operational excellence, and people leadership for a large, global organization (100+ FTEs). Responsibilities include shaping long-range vision, overseeing end-to-end delivery of C&SP activities, managing functional inputs into regulatory submissions, and leading a global leadership team. Requires 15+ years of experience in statistical programming or related areas within pharma/clinical research, with significant people leadership experience and expertise in regulatory guidelines and clinical development processes. | — | 0 |
| Expert Non‑Chromatographic Analytical Technologies & Coach Expert Non-Chromatographic Analytical Technologies & Coach for the Quality Control team in Geel, Belgium. This role supports the Janssen Innovative Medicine Supply Chain site, focusing on end-to-end technical and compliance oversight for non-chromatographic laboratories. Responsibilities include supporting daily operations, leading investigations, improving GMP procedures, acting as a subject matter expert and coach, driving continuous improvement, coordinating lifecycle management, supporting equipment, and contributing to inspection readiness. | — | 0 |