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 |
|---|---|---|
| GTO LCM Principal Process Engineer This role is for a Principal Process Engineer in the healthcare industry, specifically focusing on supporting complex production and processing equipment for medical devices. The engineer will manage technical qualifications of external manufacturers, resolve complex technical issues, lead projects, and provide technical leadership and mentoring. The role involves translating project concepts into deliverables, partnering with New Product Development, and ensuring compliance with GMP, GDP, and quality systems. Experience in process engineering, medical device production, and project management is required. | — | 0 |
| TPO - IMT Supply Chain Plan Data Assets The Technical Product Owner (TPO) – Plan Data Assets is accountable for the technology delivery, deployment, and operational support of Bronze, Silver and Gold data assets for the Plan function. The role leads a dedicated technical squad and partners closely with the Data Product Owner, Information Architect, Solution Architect, and engineering leadership to ensure Plan data assets are fit‑for‑purpose, compliant, scalable, and delivered through modern CI/CD practices. The TPO balances feature delivery with platform standards and technical debt management, ensuring Plan data assets meet defined quality, governance, and performance expectations while enabling reliable downstream analytics, AI, and business decision‑making. The role also involves applying AI and GenAI literacy to identify opportunities where Plan data assets can support AI‑enabled analytics, semantic search, and insight generation. |
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| Software Quality Engineering Lead Lead Software Quality Engineering role at Johnson & Johnson focused on ensuring compliance and quality for medical device software projects. Responsibilities include managing direct reports, reviewing software deliverables, providing expertise in verification and validation, and collaborating with project teams to meet global standards and regulations. | — | 0 |
| Cloud Network Design Engineer This role is for a Cloud Network Design Engineer at Johnson & Johnson, focusing on establishing and maintaining network infrastructure, developing next-generation network solutions in areas like SDN/NFV, SDWAN, and cloud networking, and collaborating with various teams for deployment and automation. The role requires a Bachelor's degree in a related field and 5 years of experience. | — | 0 |
| Senior Manager, Industrial Design Senior Manager, Industrial Design for the Robotics and Digital R&D Team at Johnson & Johnson MedTech. This role involves leading a team of 5-6 industrial designers, shaping surgical robotic systems like Ottava and Monarch, and exploring future medical robotics. The position requires collaboration with engineering and marketing, overseeing project planning from concept to launch, and advocating for a long-term user experience vision. The ideal candidate has 10+ years of experience in industrial design, leading complex products through the full development lifecycle, and strong leadership and communication skills. | — | 0 |
| GTO LCM Senior Process Engineer Senior Process Engineer at Johnson & Johnson in Nijmegen, Netherlands, focusing on the Life Cycle Management (LCM) of medical device manufacturing processes. Responsibilities include providing technical support, managing external manufacturer qualifications, resolving technical issues, leading projects, and ensuring process optimization and validation within a GMP environment. | — | 0 |
| Senior Supplier Engineer This role is for a Senior Supplier Engineer in the healthcare industry, focusing on electronic components and assemblies. The engineer will be the primary technical contact with US-based suppliers, leading initiatives for product development, second-sourcing, and establishing quality programs. Responsibilities include managing engineering projects, analyzing manufacturing processes, developing yield improvement plans, assessing risks with FMEAs, and creating process validation plans (IQ/OQ/PQ). The role also involves collaborating with internal design and inspection teams, supporting product development projects, and influencing design for manufacturing and test (DFM) improvements. Experience with FDA regulations (21CFR820/821) and ISO 13485 is required. | — | 0 |
| Manufacturing Operator Manufacturing Operator role at Johnson & Johnson focused on executing routine tasks to support internal operational teams in pharmaceutical process operations. Responsibilities include following SOPs, ensuring GMP compliance, monitoring resources, maintaining records, and contributing to continuous improvement. Requires an MBO-2 degree or equivalent experience, proficiency in Dutch or English, and basic MS Office skills. | — | 0 |
| Senior Site Manager (SSU) This role is for a Senior Site Manager in R&D Operations, specifically Clinical Trial Support, at Johnson & Johnson. The primary responsibility is to act as the main contact between the sponsor and investigational sites, ensuring compliance with protocols, SOPs, GCP, and regulations from study start-up to closure. Key activities include site selection, initiation, monitoring (on-site and remote), subject recruitment planning, data management, AE/SAE reporting, and site close-out. The role also involves ensuring site staff training, managing study supplies, and collaborating with internal teams and external stakeholders. There's an opportunity to mentor junior staff and contribute to process improvements. | — | 0 |
| Evergreen Global Trial Associate This role provides administrative and logistical support for clinical trials, including tracking progress, managing study data, organizing meetings, and ensuring compliance with SOPs and regulatory requirements. It involves site feasibility, maintaining electronic trial master files, and supporting study start-up, monitoring, and close-out activities. | — | 0 |
| Evergreen Deliver Management Trainee Support the needs of the department, work cross-functionally to optimize operations to enhance warehousing and transportation efficiency, improve customer service satisfaction and order fulfillment rate. | — | 0 |
| Manufacturing Excellence & Digital Specialist This role drives operational excellence and digital transformation in manufacturing by integrating Lean Manufacturing principles, process optimization, and digital solutions, with a focus on the Manufacturing Execution System (MES). It supports MES implementation, deployment, and post-go-live support, aiming to enhance quality, cost, delivery, and team efficiency. The role bridges Manufacturing, Quality, and IT, promotes Lean culture, and leverages digital tools for efficiency and compliance. | — | 0 |
| Evergreen Global Trial Associate This role provides administrative and logistical support for clinical trials at Johnson & Johnson, focusing on tracking trial progress, managing study data, organizing meetings, and ensuring adherence to SOPs and regulatory requirements. It involves site feasibility, maintaining electronic trial master files, and supporting study start-up and close-out activities. | — | 0 |
| QA Specialist (Contractor) QA Specialist role focused on ensuring Quality & Compliance and Quality Systems execution in compliance with local regulatory requirements and J&J policies and standards within the North Asia region (HK, TW, KR). Responsibilities include QMS compliance, CAPA/Change Control/Audit management, quality documentation, complaint handling, safety compliance, and supplier quality management. Requires understanding of QMS and regulatory requirements, with 1-3 years of experience in the healthcare or regulated industry. | — | 0 |
| Sr Mgr Project Engineering Lead engineering and design activities for large capital infrastructure projects at Johnson & Johnson, focusing on alignment with business objectives and project delivery practices. This includes defining project requirements, preparing RFPs, leading design development, and coordinating with internal and external teams to ensure projects are delivered according to plan. | — | 0 |
| Ausbildung zum/zur Mechatroniker*in (m/w/d) Apprenticeship program for Mechatronics Technician (m/w/d) at Johnson & Johnson in Norderstedt, Germany. The role involves building and maintaining production machinery, manufacturing mechatronic systems, and working with mechanical, electronic, pneumatic, and hydraulic components. It also includes programming machine control systems and reading technical drawings. The program is 3.5 years long and offers above-average compensation and social benefits. | — | 0 |
| Manufacturing Operator/ DSP Manufacturing Operator role in pharmaceutical process operations at Johnson & Johnson, focusing on routine production activities, process monitoring, documentation, and continuous improvement within a regulated environment. | — | 0 |
| [IT] Order to Cash (O2C) Product Manager [Shockwave] This role is for an Oracle Order to Cash (O2C) System Analyst at Johnson & Johnson in Tokyo. The primary responsibility is to design, implement, and support Oracle Cloud ERP functionalities related to order management, invoicing, and accounts receivable. The role requires extensive experience with Oracle ERP (EBS/Cloud) implementations, specifically in Order Management, Billing, Pricing, and Customer setups, as well as integrating with CRM applications like Salesforce and 3PL partners. The analyst will translate business needs into scalable solutions, manage O2C system issues, and collaborate with cross-functional teams. | — | 0 |
| Sr. Data Engineer Sr. Data Engineer responsible for designing, building, and maintaining data pipelines using technologies like Fivetran, Databricks, Python into Snowflake, and transforming data using dbt and Coalesce. The role involves ensuring data quality, security, and performance, creating dashboards in Power BI, and implementing data observability tools like Monte Carlo. | — | 0 |
| Regional SC Planner The Regional Supply Chain Planner role at Johnson & Johnson focuses on executing end-to-end supply chain initiatives for the Medtech business in the APAC region. This involves managing operational planning, driving supply chain optimization, assessing risks, and implementing improvements using digital tools like Python, Power BI, KNIME, and Copilot. The role requires strong analytical and problem-solving skills, stakeholder management, and a deep understanding of supply chain planning processes. | — | 0 |
| Principal Quality Engineer Principal Quality Engineer at Johnson & Johnson (Biosense Webster) responsible for establishing and maintaining policies and procedures for regulatory compliance (FDA, ISO 13485, environmental), developing quality control and risk management plans, using statistical tools (Six Sigma, DOE) for data analysis and process improvement, participating in new product development and introduction (NPD/NPI) teams, supporting LCM activities (IQ/OQ/PQ), conducting failure mode and effects analysis (FMEA), and ensuring product acceptance and transfer to manufacturing. Requires a Bachelor's degree in Mechatronics Engineering, Manufacturing Engineering, or related field and 6 years of experience. | — | 0 |
| Maintenance Technician The Maintenance Technician at Johnson & Johnson will perform maintenance, calibration, and troubleshooting of equipment in a manufacturing environment. Responsibilities include preventive and corrective maintenance, documentation, spare parts management, line support, and participating in improvement projects, all while adhering to GMP and safety standards. | — | 0 |
| Associate Director, Clinical Science (Robotics & Digital Solutions) - MedTech Surgery Associate Director, Clinical Science for a Robotic Surgical System (OTTAVA platform) at Johnson & Johnson. This role involves leading a team of clinical scientists to develop and deliver clinical evidence strategies aligned with regulatory and commercial needs, contributing to study design, implementing real-world evidence, and managing regulatory submissions for medical devices. The role requires strong leadership, scientific expertise, and experience in clinical research and product development processes within the healthcare industry. | — | 0 |
| Principal Electrical Engineer Principal Electrical Engineer for a robotic surgical platform (MONARCH®) at Johnson & Johnson. Focus on PCB design, electrical system architecture, and medical device safety standards (IEC 60601). Responsibilities include leading design, ensuring compliance, and providing technical leadership for complex electronic systems in a regulated medical device environment. | — | 0 |
| Sr Mgr Project Engineering This role is for a Sr. Manager of Project Engineering at Johnson & Johnson, focusing on leading engineering and design activities for large capital infrastructure projects. Responsibilities include defining project requirements, preparing RFPs, leading design phases, collaborating with suppliers and internal teams, and ensuring compliance with J&J standards and regulatory requirements. The role requires a Bachelor's degree in Engineering and 8 years of experience in capital facility projects. | — | 0 |
| Sr Mgr Project Engineering Johnson & Johnson is seeking a Sr Manager Project Engineering to lead engineering and design activities for large capital infrastructure projects. This role involves defining project requirements, managing RFPs, coordinating design development, and ensuring compliance with J&J standards and regulatory requirements. The manager will also contribute to regional operational strategies and talent development. | — | 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. | — | 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 |
| 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 |
| 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 |
| 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 |
| Engineering Technician Engineering Technician role focused on maintaining, fault finding, and repairing CNC machines in a regulated medical device production environment. Requires strong mechanical and electrical skills, experience with CNC controls, and adherence to GMP/ISO quality practices. | — | 0 |
| Supplier Quality Engineer Supplier Quality Engineer role focused on managing suppliers from a quality perspective, conducting assessments, ensuring compliance with quality requirements, managing corrective actions, and overseeing product launches/transfers at strategic suppliers. This role involves collaboration with internal and external stakeholders, including manufacturing, quality engineers, suppliers, and auditors. | — | 0 |
| Director, Reliability Engineering Director of Reliability Engineering for the Robotics and Digital R&D Team at Johnson & Johnson MedTech, focusing on advanced robotic platforms for surgery. The role involves leading a team of reliability, electrical, and mechanical engineers to ensure hardware reliability, define strategies, and oversee testing and characterization, while adhering to medical device regulations. | — | 0 |
| Technical Product Owner, ServiceNow Platform Solutions Technical Product Owner for ServiceNow Platform Solutions at Johnson & Johnson, focusing on HR, Procurement, and Finance global services. Responsibilities include leading daily execution, designing and delivering technology solutions, managing product roadmaps, and collaborating with business and technology partners. The role involves end-to-end ownership of ServiceNow products, prioritizing features, defining user stories, and implementing agile principles. | — | 0 |
| [MedTech] Transport & Trade Operations Manager, Integrated Supply Chain, Deliver Japan The Transport & Trade Operations Manager is responsible for managing import and export operations, ensuring compliance with regulations, monitoring KPIs, managing freight costs, and collaborating with cross-functional stakeholders. This role requires experience in supply chain management, people management, and supplier management, with a strong emphasis on trade compliance and operational efficiency. | — | 0 |
| Manager- ServiceNow Solution Architect Manager-level ServiceNow Solution Architect at Johnson & Johnson, responsible for designing and implementing scalable, secure solutions within their enterprise ServiceNow platform. The role emphasizes technical judgment, platform sustainability, and hands-on solution quality in a large-scale, highly governed environment, with a focus on configuration over customization and supporting upgrade readiness. Collaboration with platform leadership on GenAI initiatives is also mentioned. | — | 0 |
| Principal Embedded Software Test Engineer - Abiomed Principal Embedded Software Test Engineer for a medical device company (Abiomed) focusing on cardiovascular solutions. Responsibilities include leading test plan development, execution of manual and automated tests for embedded software, collaborating with engineering teams, enhancing test automation frameworks and CI/CD pipelines, and mentoring junior members. Requires experience with embedded platforms, real-time operating systems, Python scripting, and understanding of FDA cybersecurity guidelines. Medical device industry experience is strongly preferred. | — | 0 |
| Sr Embedded Software Test Engineer - Abiomed Senior Embedded Software Test Engineer for medical devices, focusing on developing and executing manual and automated test plans, enhancing test automation frameworks and CI/CD pipelines, and performing root cause analysis. Requires experience with embedded platforms, real-time operating systems, Python scripting, and familiarity with cybersecurity guidelines and DevOps tools. | — | 0 |
| Senior Manager, R&D Software Engineering Senior Manager, R&D Software Engineering for a medical device Vision team, leading a team in the development of safety-critical medical device applications and embedded software systems. Responsibilities include guiding architecture, design, development, integration, and ensuring compliance with regulatory standards like FDA 21 CFR Part 820 and IEC 62304. The role involves project management, talent development, and hands-on troubleshooting. | — | 0 |
| Senior Manager Clinical Operations Johnson & Johnson is seeking a Senior Clinical Research Manager to manage a team of Local Trial Managers, Site Managers, and Clinical Trial Assistants. The role focuses on trial delivery in oncology, site engagement, staff development, training, onboarding, and resource management. Responsibilities include overseeing trial execution from feasibility to close-out, ensuring quality, timelines, and compliance with SOPs, HCC, and local regulations. The role also involves contributing to country strategy, optimizing ways of working, driving innovation, and continuous improvement. | — | 0 |
| PI Lead Lead PI Engineer role in Supply Chain Engineering at Johnson & Johnson, focusing on the Aveva PI system for manufacturing automation. Responsibilities include configuring interfaces, ensuring compliance with cG(a)MP, leading projects, developing global standards, and transforming the site with digital technology. Requires a Bachelor's degree in engineering and 6+ years of experience in a GxP regulated environment, with specific experience in Aveva PI. | — | 0 |
| Supervisor, Quality Control Microbiology Supervisor for Quality Control Microbiology department at Johnson & Johnson in Schaffhausen, Switzerland. Responsibilities include leading a team of up to 10 employees, ensuring smooth operation of microbiological laboratory activities, driving quality improvements, supporting investigations, and ensuring inspection readiness. Requires a degree in a related scientific field, several years of experience in microbiology quality control in regulated environments, and strong communication skills. Fluency in German and English is required. | — | 0 |
| Technicus This role is for a Medical Device Technician at Johnson & Johnson in Amersfoort, Netherlands. The technician will be responsible for performing pre- and post-tests on medical devices, troubleshooting technical issues, disassembling and assembling devices, documenting work in Salesforce, and managing spare parts inventory. The role requires technical experience, attention to detail, a collaborative mindset, and proficiency in English. Experience with Salesforce and MS Office is a plus. | — | 0 |
| Senior Scientist Clinical Pharmacokinetics The Senior Scientist Clinical Pharmacokinetics (PK Scientist) role is responsible for end-to-end Phase 1 study execution, including protocol development, pharmacokinetic/pharmacodynamic data analysis, and generating reports for clinical study reports and regulatory submissions. The role also supports other study phases with non-compartmental analysis and mentors junior scientists. | — | 0 |
| Manufacturing Operator Johnson & Johnson is seeking Manufacturing Operators for their new Lenti Viral Vector Facility in Sassenheim, Netherlands. The role involves supporting the installation and operation of new equipment, performing process and GMP documentation, and working safely in a BSL2 environment under GMP and EHS standards. The position requires experience in biotech or biopharma manufacturing, preferably with an MBO 4 or HBO education in a relevant field. | — | 0 |
| [Innovative Medicine] 生産物流本部 富士工場 オペレーションスタッフ This role is for an Operations Staff member in pharmaceutical manufacturing at Johnson & Johnson's Fuji plant in Japan. The primary responsibilities include leading inspection, manufacturing, and preservation operations according to correct procedures to ensure continuous production of quality products. The role involves managing production schedules, driving operational efficiency, safety, and quality control, and actively participating in factory improvement initiatives. Compliance with GMP and other regulations is critical. Experience with GMP/CGTP, Lean, or Six Sigma is preferred. | — | 0 |
| [Innovative Medicine] Specialist, Quality System 3 Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant) This role is a Specialist in Quality System within the Quality Operations Department at Johnson & Johnson's Fuji Plant. The primary responsibilities include managing GMP/GCTP activities such as risk assessments, investigations, CAPA, and change control. The role also involves supporting other team members, troubleshooting deviations, and leading or supporting improvement initiatives. A degree in Pharmacy, physics and chemistry, or biology is preferred, along with over 5 years of experience in quality control, quality assurance, or regulatory compliance in the pharmaceutical industry. Knowledge of GMP/GQP/QMS quality systems and business-level English proficiency are also desired. | — | 0 |
| Principal Scientist(MSAT)首席科学家-常州/苏州/上海 The Principal Scientist (MSAT) at Johnson & Johnson provides technical support for New Product Introduction (NPI), Life Cycle Management (LCM), process improvements, and new technology deployment within the Supply Chain Manufacturing division. This role involves technical assessment, due diligence, onboarding, process fit assessment, managing tech transfers, leading characterization and PPQ batches, and supporting regulatory audits. The scientist will also contribute to process optimization, cleaning validation, and cross-contamination assessments, ensuring operational discipline, safety, and quality. | — | 0 |
| Team Lead, Source Quality Team Lead for Source Quality Engineering role at Johnson & Johnson, focusing on applying quality engineering tools and methods (Six Sigma, Lean) to new product introductions, process improvements, risk management, root cause analysis, and quality control plans. The role involves mentoring and supervising junior engineers. | — | 0 |