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 53% 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 |
|---|---|---|
| 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. |
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| 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 |
| 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 |
| 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 |
| 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 I Clinical Programming Lead (Hyderabad/Bangalore/Mumbai) Senior I Clinical Programming Lead at Johnson & Johnson, responsible for planning, programming strategy, coordination, oversight, and execution of team activities in clinical data analysis and reporting. This role involves designing and developing programs, supporting submission activities with CDISC compliant data packages, and providing technical guidance to programming teams. The role requires expertise in programming languages like SAS, SQL, and Python, adhering to industry standards and regulatory requirements. | — | 0 |
| Lead Product Security Engineer Lead Product Security Engineer at Johnson & Johnson focusing on cybersecurity for medical devices throughout the product lifecycle, including pre-market and post-market activities, compliance, and risk management. | — | 0 |
| Principal Buyer/Planner - Shockwave Medical Principal Buyer/Planner for Shockwave Medical at Johnson & Johnson, responsible for procuring and planning goods and services for R&D and production of medical devices. This role involves supplier relationship management, negotiation, inventory management, and ensuring compliance with regulatory requirements. | — | 0 |
| Director, Chief Architect, Architecture The Director, Chief Architect, Enterprise Architecture serves as the senior technology architecture leader for DePuy Synthes, defining and governing enterprise-wide architecture strategy to enable business growth, innovation, scalability, and security. This role partners closely with business, IT, and digital leaders to ensure technology investments align to enterprise strategy and deliver measurable value. The role plays a critical leadership position during the evolution to a standalone DePuy Synthes organization, shaping future-state architecture and enabling operational readiness and reports into the DePuy Synthes Technology organization. | — | 0 |
| R&D Project Manager R&D Project Manager at Johnson & Johnson MedTech Cardiovascular, responsible for leading the development and worldwide launch of cutting-edge medical device products. The role involves managing multi-disciplinary teams, contractors, project timelines, and ensuring compliance with regulations and standards. | — | 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 performing technical reviews of security controls, evaluating risk scenarios, identifying and rating cyber issues, and driving process improvements. The role also requires communication of risk assessment results to senior leaders and mentoring junior team members. | — | 0 |
| Staff Image Quality Engineer Staff Image Quality Engineer at Johnson & Johnson to tune ISP pipelines for robotic endoscopy, lead the development and implementation of objective and subjective image quality metrics and algorithms for camera pipelines, and own algorithm development, IQ evaluation methodology, and tuning validation. | — | 0 |
| Reliability Test Engineer - Robotics Reliability Test Engineer for a Robotics and Digital solutions group focusing on developing advanced robotic platforms for surgery. Responsibilities include translating requirements into test protocols, developing and executing tests (mechanical, thermal, electrical, environmental), designing test fixtures, and automating test processes using scripting languages like Python or LabVIEW. The role requires strong data analysis and problem-solving skills, with experience in regulated industries being preferred. | — | 0 |
| J&J Surgery Cincinnati: Electrical Engineering Co-op, Fall 2026 Electrical Engineering Co-op role at Johnson & Johnson's Ethicon business in Cincinnati, OH, focusing on developing surgical instruments, robotics, and related electronic systems. Responsibilities include testing, experimentation, validation, design support, data acquisition and analysis, troubleshooting, and prototype fabrication. The role offers product development experience in circuit design, firmware/software, PCB design, system prototyping, and testing. | — | 0 |
| J&J Surgery Cincinnati: Design & Development Co-op, Fall 2026 This is an R&D Design & Development Co-op position within Johnson & Johnson's MedTech sector. The role involves performing testing, experimentation, and validation to support product design, contributing to design solutions using CAD and simulation tools, and assisting in developing laboratory testing and interpreting data. The position is for students pursuing degrees in engineering fields and requires a minimum GPA of 3.0. | — | 0 |
| Sr QA Associate CSQ Lab This role is for a Sr. QA Associate in a Clinical Supply Quality Laboratory at Johnson & Johnson, focusing on ensuring compliance and operational quality for clinical laboratories. Responsibilities include reviewing and approving documents, supporting audits, managing quality investigations, and contributing to quality metrics. The role requires experience in a laboratory environment, understanding of pharmaceutical product development, and strong communication skills. | — | 0 |
| MedTech_Assistant Supply Chain Manager_Vision Care Assistant Supply Chain Manager for Vision Care in Taipei City, Taiwan, responsible for end-to-end logistics operations including warehouse & distribution, inbound freight, and trade compliance. The role focuses on meeting customer expectations, optimizing supply chain performance, enabling compliant business growth, deploying digital tools and automation, managing 3PL relationships, and ensuring cost management and profitability. Requires a Bachelor's degree, 10-15 years of experience in supply chain/warehouse/distribution, and strong collaboration, problem-solving, and compliance skills. | — | 0 |
| Staff Field Reliability Engineer Staff Field Reliability Engineer for a Robotics and Digital R&D Team at Johnson & Johnson MedTech. The role involves analyzing field and internal test data, performing root-cause investigations, and strengthening product reliability. Responsibilities include defining field reliability metrics, establishing monitoring infrastructure, and partnering with various engineering and field teams to reduce customer-impacting issues and verify corrective actions. | — | 0 |
| Clinical Trials Assistant- Shockwave (Reducer) This role supports clinical trial operations by managing study supplies, processing payments, maintaining documentation, and facilitating communication within the clinical study team. It requires administrative and organizational skills, with a preference for experience in clinical research or a relevant scientific area. | — | 0 |
| Senior Manager Embedded Software Engineering, R&D Senior Manager of Embedded Software Engineering leading a team responsible for designing, developing, testing, and maintaining embedded software systems for medical devices, with a focus on cardiovascular solutions. The role involves technical leadership, strategic oversight, and ensuring compliance with standards like IEC 62304. | — | 0 |
| Principal Quality Engineer, Design Assurance – Shockwave (Reducer) Principal Quality Engineer (Design Assurance) for a medical device company (Shockwave Reducer) focused on ensuring medical devices are designed, developed, and transferred to manufacturing in compliance with quality system and regulatory requirements. Responsibilities include leading quality assurance for new product development, partnering with R&D and other teams, managing risk, overseeing V&V, supporting design transfer, and participating in regulatory audits and submissions. | — | 0 |
| Associate Manufacturing Operator Entry-level Associate Manufacturing Operator at Johnson & Johnson in Leiden, Netherlands. This role supports manufacturing operations by executing defined tasks, following standard procedures, and ensuring accuracy and quality of deliverables. Requires an MBO-2 degree with relevant experience or a non-relevant MBO-2 degree with more experience, basic Dutch or English proficiency, and flexibility for shift work. Focuses on GMP compliance and process adherence. | — | 0 |
| LCM System Engineer – Testers & Calibration Systems Johnson & Johnson MedTech Cardiovascular is seeking an LCM System Engineer to manage the full lifecycle of Testers & Calibration systems, including EOL processes, upgrades, and improvements. The role involves leading POD activities for hardware, software, and process updates, developing production support systems, and driving Cost Improvement Projects (CIP) to enhance yields, quality, efficiency, and cost-effectiveness. The position requires a B.Sc. in Engineering, minimum 3 years of experience as a System Engineer, strong electronics knowledge, debugging capabilities, and basic software understanding. Experience in manufacturing support, particularly in medical devices, is an advantage. | — | 0 |
| Polyvalent technieker (nadruk M&R) Polyvalent technician for chemical production plants, responsible for maintenance, repairs, and supporting the implementation of technological solutions to ensure continuity and optimize equipment lifecycle. Focuses on mechanical and electrical maintenance, root cause analysis, and technical expertise for specific production installations. | — | 0 |
| [MedTech] Manager, CS Enablement, CKAM, Surgery/Cardio CS, Deliver, Integrated Supply Chain Manager for Customer Service Enablement within the MedTech sector, focusing on supply chain operations, process improvement, and team management. The role involves achieving KPIs, enhancing customer satisfaction, and collaborating with internal and external stakeholders to build an efficient and reliable supply chain. Key responsibilities include team leadership, developing growth strategies, coaching staff, managing resources, and driving automation initiatives. | — | 0 |
| [Innovative Medicine] 生産物流本部 富士工場 エンジニアリング部 エンジニア This role is for a Project Engineer in the Engineering Department at Johnson & Johnson's Fuji Plant in Shizuoka, Japan. The engineer will be responsible for the engineering, design, introduction, modification, and automation of manufacturing facilities and computer systems, as well as capital project execution. Key responsibilities include technical performance assurance of production equipment (validation), stable operation design for inspection machines, packaging lines, and computer systems, improvement of manufacturing facilities based on OEE, automation, and digital transformation, and vendor supervision. The role also requires supporting EHS policies and providing technical leadership. Compliance with GMP/GCTP, company policies, and regulations is mandatory. Desired experience includes working in pharmaceutical, cosmetic, or food industries, and business-level English proficiency. | — | 0 |
| Senior Reliability Engineer Senior Reliability Engineer at a large small molecule API production site, focusing on improving manufacturing equipment reliability and performance through data analysis, root cause elimination, and digital solutions. The role involves developing asset plans, leading reliability projects using methodologies like RCM, and collaborating with Operations, Engineering, Quality, and Maintenance. | — | 0 |
| Senior Product Development Engineer Surgical Robotics – OTTAVA Senior Product Development Engineer for Surgical Robotics at Johnson & Johnson, focusing on New Product Development (NPD) and New Product Introduction (NPI) for medical devices. The role involves collaborating with cross-functional teams and suppliers to develop, qualify, and stabilize component, equipment, and manufacturing processes, ensuring robust designs and manufacturability. Responsibilities include DFM/DFA, tolerance analysis, cost optimization, design reviews, and supporting Design Transfer and GMP compliance. | — | 0 |
| Staff Packaging Engineer: Surgical Robotics – OTTAVA Staff Packaging Engineer for Surgical Robotics (OTTAVA) at Johnson & Johnson, focusing on the design, development, testing, and validation of packaging systems for medical devices, including robotic capital equipment. The role requires ensuring product quality, regulatory compliance, manufacturability, and cost-effectiveness within a regulated medical device environment, collaborating with cross-functional teams and suppliers. | — | 0 |
| Senior Technical Safety Engineer Senior Technical Safety Engineer role within Global Engineering and Technology (GET) group at Johnson & Johnson Innovate Medicine, based in Geel, Belgium. Focuses on technical safety aspects of equipment in a chemical production site for Active Pharmaceutical Ingredients (APIs). Responsibilities include owning technical safety processes, providing expert advice, and driving improvements across assets. Requires a Masters level Engineering degree in chemical/process safety engineering and skills in technical safety aspects, decision-making, and innovative solutions. | — | 0 |
| MES Program Lead Lead the delivery of MES (Manufacturing Execution System) related programs for CAR-T manufacturing sites, focusing on capacity expansion, operational alignment, and regulatory compliance. This role involves managing project governance, cross-functional coordination, and issue resolution to ensure life-saving products reach patients. | — | 0 |
| Manager, Systems Integration - Robotics Manager for Systems Integration in Robotics, focusing on operating, troubleshooting, and maintaining a complex robotic system (OTTAVA) within R&D. The role involves leading a team of technical specialists, driving functional excellence, managing technical risks, and collaborating cross-functionally for product development. Requires technical and leadership experience with complex electromechanical systems. | — | 0 |
| CAR-T Manufacturing Operator Johnson & Johnson is seeking a CAR-T Manufacturing Operator in Raritan, NJ. This role involves performing manufacturing procedures and executing tasks within a CGMP environment, handling patient materials (blood, viruses, cells) in a cleanroom setting with appropriate PPE. Responsibilities include executing cell culturing, purification, aseptic processing, cryopreservation, welding, sealing, and accurate data recording according to GDP and ALCOA+ standards. The role requires working in a team, supporting process improvements, handling human-derived materials in containment areas, and maintaining a clean and safe work environment. Aseptic qualification and adherence to cGMP are critical. The role involves standing for long periods and working within a dynamic shift schedule. | — | 0 |
| Aseptic Manufacturing Operator CAR-T The CAR-T Aseptic Manufacturing Operator is responsible for the formulation and filling of final cell therapy products or preparation of components used for cell therapy products within a GMP-compliant cleanroom environment. This role requires expertise in aseptic techniques, attention to detail, and strict adherence to GMP and regulatory requirements to produce a safe and effective cell therapy. | — | 0 |
| [Innovative Medicine] Specialist, Quality System 2 Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant) This role is a Specialist in Quality System at Johnson & Johnson's Innovative Medicine division in Japan. The primary responsibilities involve ensuring compliance with GMP/GCTP regulations, managing quality systems, data integrity, deviation control, and change control. The role also involves acting as a point of contact with marketing authorization holders, supporting other team members, troubleshooting, and leading or supporting improvement initiatives. A degree in a scientific field and experience in pharmaceutical quality control/assurance/compliance are desirable. | — | 0 |
| Manufacturing Operator Manufacturing Operator role at Johnson & Johnson focused on the preparation and manufacture of active pharmaceutical ingredients, intermediates, and/or medical devices. Responsibilities include operating and cleaning production equipment, following standard operating procedures, maintaining documentation, and ensuring quality, safety, and environmental compliance in a regulated pharmaceutical environment. | — | 0 |
| QA Ops Platform Lead The QA Operation Platform Lead is responsible for end-to-end quality management for product families, from supplier selection and qualification through transfer to production and maintaining supplier and process control during the product lifecycle. This role supports quality-related activities, manages process validation, supports change control, and leads improvement plans with suppliers. | — | 0 |
| Senior Manager, Vector Biology Senior Manager role focused on advancing viral vector biology, vector design improvements, assay development, and optimization of lentiviral vectors for in vivo cell targeting within Johnson & Johnson's Innovative Medicine division. The role involves leading a multidisciplinary team, providing technical leadership, and strategic direction to enhance cell-specific transduction capabilities. | — | 0 |
| Optics Operator I (Multiple Positions) This role is for an Optics Operator I at Johnson & Johnson, responsible for performing various tasks on a manufacturing line, operating general manufacturing equipment, and ensuring compliance with specifications and standards. The role involves maintaining a clean and organized work area, documenting production data, and completing transactions in the manufacturing system. A high school diploma and availability for overtime and various shifts are required. | — | 0 |
| Director, Manufacturing. Site Leader/Surgical Robotics - OTTAVA Director, Manufacturing Site Leader for the OTTAVA Surgical Robotic Platform, responsible for strategic, operational, and technical leadership of manufacturing plants. This role oversees daily operations, long-term planning, talent development, and drives initiatives to improve safety, quality, productivity, and scalability, including scaling production from pilot to high-volume output while maintaining quality. | — | 0 |
| Associate Field Service Engineer Develop customer-centric service and repair strategies for medical capital equipment, shape a robust framework for service excellence, and provide foundational service and repair engineering and technical support to customers and stakeholders. | — | 0 |
| Sr Engineer, Automation Applications/Surgical Robotics - OTTAVA Seeking a Senior Engineer to architect, develop, and deploy scalable automation solutions for manufacturing operations, including robotic cells, AMRs, and IoT-enabled workflows. The role involves end-to-end delivery from concept to commissioning, system design, integration of hardware/software, machine safety, and OT/IIoT connectivity. Experience with industrial robots, PLCs, and regulated industries is required. | — | 0 |
| Staff Data Engineer/Surgical Robotics - OTTAVA Staff Data Engineer role focused on building data foundations and pipelines for manufacturing and supply chain operations, connecting shop-floor systems to cloud solutions. Responsibilities include data architecture, ETL/ELT pipeline development using Databricks and AWS, data quality, observability, and ensuring compliance with validation standards. | — | 0 |
| Lead Clinical Data Analyst Lead Clinical Data Analyst role at Johnson & Johnson's DePuy Synthes team, focusing on the implementation and maintenance of clinical systems, including EDC, CTMS, eTMF, and IxRS. Responsibilities involve project management, vendor evaluation, process development, and ensuring compliance within clinical research for medical devices. | — | 0 |