Johnson & Johnson
Pharma · Pharma + medtech
- HQ
- New Brunswick, US
- Founded
- 1886
- Size
- 130,000+
- Website
- jjmt.com.tw
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 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.
Pharma · Pharma + medtech
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 |
|---|---|---|
| Product Security Manager The Product Security Manager will implement Johnson & Johnson's enterprise Product Security strategy and framework for the Vision medical device portfolio. Responsibilities include supporting new product development, reviewing security requirements, recommending design solutions, conducting threat modeling, penetration testing, code analysis, and managing post-market security for marketed devices. This includes monitoring vulnerabilities, assisting with remediation, responding to customer questionnaires, and reviewing contractual agreements. The role also involves driving adherence to the Product Security framework, creating metrics, and enforcing governance. | — | 0 |
| Senior Manager, Global CAPA Management Senior Manager, Global CAPA Management role at Johnson & Johnson, focusing on ensuring the implementation and global improvement of investigation and corrective and preventive action (CAPA) processes within the Innovative Medicines sector. This role involves liaison with technical teams for QMS platform development, continuous improvement of the CAPA QMS platform, and leadership in change management and quality system integration. The position requires ensuring compliance with GxP and other regulatory requirements. |
| — |
| 0 |
| Senior Quality Specialist This role is responsible for leading and supporting Global Compliance activities related to change control and document control processes within Johnson & Johnson's healthcare sector. It involves providing subject matter expertise for integrating new projects into enterprise systems, enhancing system capabilities, and troubleshooting electronic systems like EDMS/PLM. The specialist will analyze metrics, identify process improvements, develop global procedures, and ensure compliance with regulatory requirements, partnering cross-functionally to maintain audit readiness. | — | 0 |
| Transcend Senior Manager Business Test Validation Seeking a Senior Manager for Business Test Validation to drive end-to-end testing cycles for SAP S/4HANA releases within a regulated pharmaceutical environment. This role involves establishing a global testing methodology, leading cross-functional teams, and ensuring compliance with GxP and CSV standards. | — | 0 |
| Senior Quality Engineer (NPD) Senior Quality Engineer for New Product Development in the medical device industry, focusing on ensuring compliance with GMP, ISO, and other applicable standards throughout the product lifecycle. Responsibilities include developing requirements, verification/validation strategies, risk management, and documentation review. | — | 0 |
| Service and Repair Sr. Quality Engineer Quality Engineer role focused on supporting Service and Repair operations within the healthcare industry, ensuring compliance with J&J standards, regulations, and quality systems. Responsibilities include managing escalations, non-conformances, CAPA, change control, and supporting audits. | — | 0 |
| Transcend Senior Manager Business Test Validation This role is for a Senior Manager of Business Test Validation for a global business transformation program modernizing foundational transactional processes into a standardized SAP S/4HANA ERP platform within a regulated pharmaceutical environment. The role focuses on driving end-to-end testing cycles, including integration testing, Business Simulation Testing (BST), user acceptance testing (UAT), performance testing, and validation activities, ensuring alignment with GxP and CSV compliance standards. | — | 0 |
| Senior Manufacturing Engineer Senior Manufacturing Engineer at Johnson & Johnson's Limerick site, supporting a high-volume, fully automated manufacturing environment. Responsibilities include the design, installation, and improvement of lens production processes and equipment, troubleshooting, leading cost and technical improvements, project management, and ensuring quality and safety compliance within an FDA-regulated environment. | — | 0 |
| Maintenance Engineering Manager, Machine Shop & Asset Management Johnson & Johnson MedTech is seeking a Maintenance Manager to lead Maintenance, Machine Shop, and Asset Management teams to ensure safe, reliable, compliant, and cost-effective manufacturing operations. The role involves developing maintenance strategies, overseeing machine shop operations, managing asset lifecycle, and partnering with other departments to maximize equipment performance. Responsibilities include leading teams, managing budgets, ensuring compliance, and coordinating breakdown responses. | — | 0 |
| Senior Quality Clerk The Senior Quality Clerk at Johnson & Johnson supports activities related to the Quality System, including managing defect tracking, document retention, records management, and product evaluations. This role also involves supporting Non-Conformance (NC) and Corrective and Preventive Action (CAPA) processes, generating reports, assisting with audits, and ensuring compliance with Good Manufacturing Practices (GMP), ISO, and QSR requirements. The position requires experience in quality control and administrative support within a regulated environment. | — | 0 |
| Programador de Produccion y Transferencias( Fixed - Term 6 Months) This role is responsible for managing the flow of raw materials and finished products in manufacturing areas, ensuring materials are handled according to production line procedures. Key responsibilities include programming production orders, balancing production lines, communicating between departments to prevent material shortages, managing production priorities, performing cycle counts, assigning components, and reconciling production orders to avoid financial impact. The role also involves managing specific product components and ensuring accurate inventory levels. | — | 0 |
| Senior CSQ Associate This role is for a Senior CSQ Associate in the Clinical Supply Quality team at Johnson & Johnson. The primary focus is on reviewing and approving complaint investigations, ensuring scientific soundness and compliance. The role also involves contributing to complex investigations, process improvements, and acting as a Quality Lead for investigations related to Clinical Supply Planning and Logistics. While the role mentions an understanding of AI concepts and frameworks for efficiency, it is not core to the job function. | — | 0 |
| MedTech Supply Chain Procurement Co-Op This is a co-op position supporting the MedTech Supply Chain Procurement Organization at Johnson & Johnson. The role involves enhancing project portfolio processes, supporting technology design and adoption, exploring digital tools for procurement and supplier collaboration, developing PMO strategies, tracking KPIs, and applying data-driven insights to sourcing decisions. The ideal candidate is an undergraduate student pursuing a degree in business, engineering, supply chain, or a related field, with strong analytical skills and technological curiosity. | — | 0 |
| Shift Support Specialist This role supports plant operations by overseeing contractor activities, managing work permits, troubleshooting issues in a regulated environment, and coordinating technical changes. It involves ensuring safety, quality, and operational efficiency on the production floor. | — | 0 |
| Senior Director, Lean Excellence Senior Director of Lean Excellence at Johnson & Johnson Vision, responsible for applying Lean Methodology and similar tools (Six Sigma, Lean) to drive significant business improvements in manufacturing site operational models. This includes developing and executing a multiyear roadmap, coaching team members and leaders, and creating a continuous improvement culture. | — | 0 |
| Eng Project Engineering - Fixed Term 24 months Project Engineering role at Johnson & Johnson focused on driving global initiatives for product families manufactured across multiple sites. Responsibilities include leading cross-functional teams, managing technical projects, solving challenges, and ensuring compliance with GMP and regulations. Requires a Bachelor's in Engineering with at least 1 year of experience in equipment/packaging/product engineering and project management, with a strong understanding of manufacturing processes and GMPs. | — | 0 |
| Operator I This role is an Operator I at Johnson & Johnson in Suzhou, China. The primary responsibilities include supporting daily production management, operating machines safely and effectively to ensure high efficiency, maintaining traceability of materials and products, balancing materials according to production plans, and completing quality records and production line activities. The role requires adherence to all applicable laws, regulations, and company procedures related to health, safety, and environmental practices. | — | 0 |
| Principal Scientist Process Johnson & Johnson is seeking a Principal Scientist to lead late-stage process development, technology transfer, and validation for biotherapeutic fill/finish manufacturing. This role requires expertise in scale-down models, process parameter evaluation, technical project management, and ensuring compliance with regulatory and cGMP standards. The scientist will act as a subject matter expert for audits and partner with cross-functional teams to define scientific strategies for new product introductions. | — | 0 |
| Operator I This role is an Operator I at Johnson & Johnson in Suzhou, China. The primary responsibilities include supporting daily production management, operating machines safely and effectively to ensure high efficiency, maintaining traceability of materials and products, balancing materials according to production plans, and completing quality records and production line activities. The role requires adherence to all applicable laws, regulations, and company procedures related to health, safety, and environmental practices. | — | 0 |
| Operator I This role supports daily production management in a manufacturing environment, focusing on operating machines safely and efficiently, maintaining traceability, balancing materials, and completing quality records and production line activities. It requires adherence to production specifications and company regulations. | — | 0 |
| Operator I Operator I role at Johnson & Johnson in Suzhou, China, focusing on supporting daily production management, operating machinery safely and efficiently, ensuring traceability, and collaborating with engineers on machine settings. Responsibilities include production work, quality record completion, and line maintenance. | — | 0 |
| Operator I Operator role at Johnson & Johnson focused on supporting daily production management, operating machinery safely and efficiently, ensuring traceability, and collaborating with engineers on machine settings. Responsibilities include production work, quality record completion, and line cleaning. This role is not directly related to AI/ML development. | — | 0 |
| Operator I Operator I role at Johnson & Johnson in Suzhou, China, focused on supporting daily production management, operating machinery safely and efficiently, maintaining traceability, and collaborating with engineers on machine settings. Responsibilities include following production schedules, completing quality records, and performing line cleaning activities. | — | 0 |
| Manager Clinical Trial Payments Manager for Clinical Trial Payments at Johnson & Johnson, responsible for overseeing regional site payments, issue resolution, and training related to clinical trial management systems (mCTMS) and payment processes. The role involves process ownership, driving continuous improvement, managing a global team, and ensuring compliance with healthcare regulations. | — | 0 |
| Global MT SC ERP Quality Manager The Quality Manager will support the MedTech SC Digital Transformation organization, focusing on modernizing supply chain digital capabilities by harmonizing ERP systems and standardizing business processes. This role will ensure the SAP S/4HANA ERP platform has the necessary support structures, processes, and governance for Quality Management. Responsibilities include serving as a primary contact for the Quality business area, building partnerships with stakeholders, supporting SAP QM process sustainment, collaborating on quality assurance policies, identifying and remediating system issues, coordinating testing, supporting security role design, managing enhancement intake, and contributing to the continuous improvement of the support model. | — | 0 |
| MSAT Synthetics DP External site Principal Scientist Johnson & Johnson is seeking a Principal Scientist for their MSAT Synthetics Drug Product External Site team. This role involves providing technical oversight to external manufacturing sites, including due diligence, auditing, and onboarding. Responsibilities include technical/risk assessment for New Product Introduction (NPI), technical transfers, and Product Life Cycle (LCM) management, as well as deploying new technologies and performing statistical analysis. The scientist will act as a primary technical contact for external manufacturers and ensure compliance with quality and regulatory standards. | — | 0 |
| Process Engineer Process Engineer at Johnson & Johnson in Limerick, Ireland, responsible for planning, executing, and delivering engineering activities within a manufacturing value stream. This role involves technical leadership to improve safety, quality, delivery, and cost, supporting new product introductions, process changes, and compliance in a highly regulated (GMP/ISO/FDA) environment. Key responsibilities include managing change control, validation (IQ/OQ/PQ), technical investigations, and driving continuous improvement initiatives in collaboration with cross-functional teams. | — | 0 |
| [Innovative Medicine] Analyst, FF Testing, Quality Control Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant) The Analyst, FF Testing, Quality Control Group at Johnson & Johnson's Fuji Plant is responsible for performing various analytical tests (chemical, microbial, packaging material), method validation, and technical transfers to ensure compliance with regulatory requirements (JP, GMP/GCTP). The role involves training other analysts, writing and reviewing laboratory documents, managing deviations, maintaining knowledge of technology and GMP/GCTP standards, managing lab equipment lifecycle, and supporting product quality reviews. A Bachelor's degree in a science field and over 3 years of experience in the pharmaceutical industry are required, along with knowledge of GMP/GCTP, pharmaceutical regulations, analytical testing, and documentation. | — | 0 |
| [Innovative Medicine] R&D, Senior Local Trial Manager, x-TA Clinical Operation, GCO Japan This role is for a Senior Local Trial Manager in Innovative Medicine R&D at Johnson & Johnson, focusing on the operational management of clinical trials within Japan. The position involves overseeing trial activities from start-up to closeout, ensuring compliance with protocols, SOPs, GCP, and regulatory requirements. Responsibilities include leading local trial teams, managing budgets, coordinating with stakeholders, ensuring timely reporting of adverse events, and contributing to process improvements and training. | — | 0 |
| [Innovative Medicine] Regulatory Affairs Intern Intern role supporting the Regulatory Affairs team in day-to-day activities related to registration, lifecycle management, and regulatory compliance within the pharmaceutical industry. Responsibilities include assisting with regulatory submission documents, labeling reviews, and ad hoc projects like regulatory intelligence research. | — | 0 |
| Experienced I Stat Programmer Experienced Statistical Programmer responsible for developing, verifying, and documenting code for clinical data analysis and reporting within the pharmaceutical industry. Supports clinical projects and submissions with a focus on quality and timeliness. | — | 0 |
| Manutentore Elettrico - Manufacturing This role is for an Electrical Maintenance Technician at a Johnson & Johnson manufacturing site in Latina, Italy. The primary responsibilities include performing preventive, corrective, and predictive maintenance on production and packaging machinery, supporting process improvement, recording activities in SAP-CMMS, interpreting equipment manuals, and applying safety and quality procedures. The role requires a technical diploma, preferably with prior experience as an electrical maintenance technician, and knowledge of electrical diagrams, diagnostic tools, programmable logic systems, and basic English. | — | 0 |
| E&PS Senior Manager, Project Management Senior Manager, Project Management for Engineering & Property Services (E&PS) at Johnson & Johnson, responsible for managing a portfolio of key projects supporting business operations and compliance initiatives within a regulated manufacturing environment. This role involves leading the planning, execution, and delivery of site capital and design/construction projects, ensuring they meet safety, quality, and budget standards. | — | 0 |
| Field Service Engineer, GBA Field Service Engineer responsible for onsite service, maintenance, and technical support for DePuy Synthes robotics systems and related digital platforms, ensuring system uptime, regulatory compliance, and customer satisfaction. This role involves installation, commissioning, preventive maintenance, troubleshooting, and customer training within hospital and laboratory environments. | — | 0 |
| Principal R&D Project Manager The Principal R&D Project Manager will plan and execute projects within the Navigation platform in Digital R&D, ensuring delivery against scope, schedule, cost, and quality in a regulated medical device environment. This role involves managing cross-functional teams, project budgets, risks, and design controls to achieve predictable delivery outcomes. | — | 0 |
| Analyst Quality Control The Quality Control Analyst is responsible for conducting biochemical, microbiological, and/or general testing of final product samples submitted to the QC laboratories, ensuring compliance with procedures, standards, and GMP regulations. This role involves performing analytical testing, data review, documentation, and supporting inspections within the biopharmaceutical industry. | — | 0 |
| NPI Test Engineer/Surgical Robotics-OTTAVA This role focuses on developing and deploying test software solutions to support the manufacturing of complex electro-mechanical components within a medical robotics system. It involves designing automated test algorithms, building scalable software infrastructure, and ensuring high standards of repeatability and validation. The position also supports troubleshooting, root cause analysis, and data-driven insights to improve manufacturing processes, while collaborating cross-functionally with design, manufacturing, and data teams in a regulated MedTech environment. | — | 0 |
| MSAT Experienced Scientist The MSAT Experienced Scientist at Johnson & Johnson is responsible for the build, development, and lifecycle management of manufacturing and packaging equipment cleaning processes within the pharmaceutical industry. This role involves leading and supporting cleaning validation activities, developing strategies, coordinating cross-functional efforts, performing risk-based evaluations, and driving continuous improvement initiatives. The position requires a Bachelor's degree with 4+ years of experience or an advanced degree with 2+ years of experience in MSAT, validation, or related technical support within a regulated industry. | — | 0 |
| Process Engineer Process Engineer role at Johnson & Johnson focused on supply chain engineering, specifically process engineering. Responsibilities include project management, PLC-based control system design and installation, equipment reliability, and coordinating activities. The role requires investigating product inquiries, implementing corrective actions, and building expertise in relevant technologies. Compliance with quality management systems (ISO 13485, ISO14001, OSHAS18001) and performing process validations are key duties. Experience with PLCs, vision systems, CIM, robotics, and automation is preferred. | — | 0 |
| R&D Electrical Engineer I - Shockwave Medical R&D Electrical Engineer I at Johnson & Johnson focused on developing innovative medical devices for cardiovascular disease treatment. Responsibilities include mixed-signal analog and digital circuit design, microcontroller and FPGA integration, schematic capture, PCB layout, prototype testing, and ensuring compliance with medical device standards and design controls. | — | 0 |
| Ingeniero de Embalaje - Contrato Plazo Indefinido Packaging Engineer role at Johnson & Johnson, focusing on generating packaging material specifications, managing official packaging lists, coordinating material functionality tests, and ensuring compliance with regulatory standards. Requires a degree in a scientific or engineering field, 1-2 years of experience in pharmaceutical, food, or chemical industries, and proficiency in Microsoft Office, Minitab, SAP, and Project. | — | 0 |
| Senior Principal Scientist, Large Molecule Drug Product Scientific Integrator Senior Principal Scientist role focused on end-to-end scientific integration for late-stage large-molecule drug product programs within the pharmaceutical industry. Responsibilities include leading cross-functional teams, defining drug product strategy, authoring regulatory submissions, and supporting manufacturing. Requires significant experience in biopharmaceutical development and CMC regulatory strategy. | — | 0 |
| Manufacturing Technician III The Manufacturing Technician III role at Johnson & Johnson focuses on operating, adjusting, and maintaining fully automated production lines in a manufacturing environment. Responsibilities include troubleshooting equipment failures, performing routine maintenance, investigating root causes of non-conformances, and participating in process improvement initiatives. The role requires technical skills in areas like PLC systems, electro-mechanical devices, and robotics, with an emphasis on maintaining safety, quality, and production guidelines. | — | 0 |
| Sr. Service Innovation Engineer This role is for a Senior Service Innovation Engineer in the MedTech division, focusing on product development, lifecycle management, and technical support for service solutions. The engineer will act as a liaison between technical groups and service departments, recommend design for serviceability, manage service procedures, and provide escalation support for complex technical issues. The role requires experience in regulated industries and project lifecycle management. | — | 0 |
| Senior Maintenance Technician Senior Maintenance Technician role at Johnson & Johnson in Leiden, Netherlands, focusing on ensuring the reliability and continuity of production and utility systems in a pharmaceutical manufacturing environment. Responsibilities include troubleshooting, maintenance, service, and optimization of equipment, adhering to GMP and safety regulations, and working within a 5-shift system. Requires MBO 4 level education in electrical engineering or measurement and control technology, with proven industrial experience. | — | 0 |
| MES SPECIALIST I This role is for an MES Specialist I at Johnson & Johnson, focusing on the Manufacturing Execution System (MES) and connected systems. Responsibilities include supporting shopfloor control, managing change requests, performing impact assessments, maintaining SOPs, mapping processes, writing documentation, training users, and participating in system configuration, testing, validation, and implementation. The role also involves monitoring interfaces, participating in QA non-conformities and CAPA actions, and ensuring compliance with health, safety, and environmental practices. The position requires a technical background, experience in system integration testing and user problem understanding, and strong communication skills. Knowledge of GMP, ISO, FDA regulations, SQL, and programming tools is preferred. | — | 0 |
| Maintenance Technician This role is for a Maintenance Technician in a pharmaceutical manufacturing environment, responsible for ensuring the reliability and continuity of production and utility systems. The job involves troubleshooting, maintenance, service, and optimization of equipment, with a strong emphasis on GMP, safety, and compliance. | — | 0 |
| Senior Injection Moulding Engineer Senior Injection Moulding Engineer role focused on providing polymer processing and engineering expertise for medical devices and pharmaceutical products. Responsibilities include project delivery, equipment and process design/installation, troubleshooting, and leading cross-functional teams for new product introductions, all within a regulated quality management system. | — | 0 |
| Staff Project Engineer Staff Project Engineer responsible for executing site-wide capital projects for manufacturing platforms and supporting systems in a regulated medical device industry. This includes equipment upgrades, product brand conversions, and new line installation/commissioning, with a focus on budget adherence, schedule execution, and technical expertise. Requires experience with formal project management tools, leading multi-functional teams, and ensuring compliance with FDA/Safety/Quality policies. | — | 0 |
| Cryopreservation Mfg Operator, CAR-T Operates manufacturing equipment and executes tasks in a cGMP environment for cryopreservation of CAR-T products. Responsibilities include cell culturing, purification, aseptic processing, and documentation according to SOPs and regulations. Requires a high school diploma with 4 years of relevant experience or a Bachelor's degree with 0-2 years of experience. | — | 0 |