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 |
|---|---|---|
| [IT] Director, MedTech Technology Regional Head, Electrophysiology and Neurovascular, APAC Director, Regional Head of Technology for MedTech Electrophysiology and Neurovascular in APAC, responsible for shaping growth strategies, modernizing platforms, and delivering digital and AI capabilities. This role involves partnering with regional leadership to develop technology as a competitive advantage, leading a business-facing technology organization, and driving AI/ML and GenAI operationalization across various business functions. The role also includes managing the technology portfolio, leading a team, and ensuring compliance. | ShipData | 7 |
| Manager, Insights Engineering & Innovation, Medical Affairs, Japan Manager leading insight analytics and AI-driven automation within Medical Affairs, focusing on GenAI, LLMs, NLP, and conversational AI. The role involves end-to-end lifecycle management of AI initiatives, from problem framing to deployment and monitoring, with a strong emphasis on operationalizing these capabilities in a regulated healthcare environment. Requires hands-on technical expertise in data engineering, ML/NLP, MLOps, and stakeholder management. |
| AgentPost-train |
| 7 |
| [Innovative Medicine] R&D, Sr. Scientist Biostatistics, Statistics & Decision Sciences Japan, Global Development The Senior Scientist, Biostatistics will support the design and execution of studies and experiments for Clinical Development and Medical Affairs programs at J&J Innovative Medicines. This role involves statistical analysis, interpretation, and reporting of data evidence, collaborating with Quantitative Sciences & Clinical Pharmacology functions. The position supports statistical aspects of business and regulatory commitments, assists program plans, and represents Statistics & Decision Sciences in various teams. The role requires proficiency in data analytics, statistical principles, R, SAS, and familiarity with AI/ML tools, applying advanced statistical techniques, and optimizing study designs. | Data | 5 |
| [Innovative Medicine] R&D, Scientist Biostatistics, Statistics & Decision Sciences Japan, Global Development Scientist supporting the design and execution of studies and experiments for Clinical Development and Medical Affairs programs, with evolving supervision. Activities require guidance from managers and project statisticians. Support is provided to statistical analysis, interpretation, and reporting or communication of data evidence towards programs for research, development, and/or marketed product needs. Collaborates with Quantitative Sciences & Clinical Pharmacology functions and other drug development scientists. Supports statistical aspects of key business and regulatory commitments and assists program plans. | Data | 5 |
| [Innovative Medicine] Project Lead, Regulatory Medical Writing, Japan Document Management Group, IB Translation Office/Publication Owner Office This role focuses on managing translation projects for clinical trial documents (Protocol, IB) and publications within Johnson & Johnson's Innovative Medicine division. A key responsibility is to transform the existing IB translation process by integrating AI translation technologies, managing CROs, and ensuring quality through proofreading. The role also involves leading cross-functional initiatives and team development. | — | 5 |
| [Innovative Medicine] R&D, Lead Payment Analyst, Site Engagement, Contract & Grants, Global Development This role is responsible for managing end-to-end investigator/site payment processes and calculations, purchase orders, and clinical trial payments within Johnson & Johnson's Innovative Medicine division. It involves acting as a liaison for issue resolution, understanding contract values, and utilizing various systems. The role also includes training study teams and new team members on payment processes and technology, with potential people management responsibilities. A key requirement is demonstrated AI literacy and the ability to apply AI tools to improve work efficiency and outcomes. | — | 1 |
| Manager/Specialist, Hematology Group, Hematology Dept, Oncology Medical Affairs Division Manager/Specialist, Hematology Group, Hematology Dept, Oncology Medical Affairs Division at Johnson & Johnson in Tokyo, Japan. Responsible for Medical Affairs (MA) activities for Janssen Hematology brands, focusing on proper usage and value maximization. Develops medical strategy, evidence generation plans, and oversees publication activities, ensuring compliance with local regulations and industry codes. | — | 0 |
| [MedTech] Specialist, CMO Office, Operational Excellence This role focuses on operational excellence within the MedTech CMO office at Johnson & Johnson. Key responsibilities include quality control of clinical and regulatory documents, managing QMS related activities like SOPs and training, overseeing J-EGC and Research Grants Office activities, managing the MIR process, and providing general business support. The role emphasizes adherence to procedures, collaboration, and process improvement. | — | 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] Staff, Quality System 2 Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant) Staff position in Quality Operations at Johnson & Johnson's Fuji Plant, focusing on quality systems and regulatory compliance within GMP/GCTP environments. Responsibilities include overseeing regulated substances, managing approvals, handling change notifications, operating recall processes, and executing new initiatives. Requires a degree in Pharmacy/Chemistry or equivalent experience, with a strong background in pharmaceutical quality and GMP. | — | 0 |
| [Innovative Medicine] R&D, Principal Statistical Programming Lead (Manager), Clinical & Statistical Programming Japan, Global Development The Principal Statistical Programming Lead will be responsible for the planning, oversight, and delivery of programming activities for clinical projects, compounds, or submissions. This role involves designing and developing programs and technical solutions for clinical research analysis and reporting, providing guidance to programming teams, and ensuring compliance with departmental processes and industry standards. The position also contributes to innovation and process improvement projects within the department. | — | 0 |
| [Innovative Medicine] R&D, Lead Local Trial Manager, Oncology Clinical Operation, GCO Japan Lead Local Trial Manager for Oncology Clinical Operations in Japan, responsible for the local management of clinical trials, ensuring data quality and compliance with protocols, SOPs, GCP, and regulatory requirements. This senior role involves coordinating local trial teams, managing budgets, and contributing to process improvement and training. | — | 0 |
| [Innovative Medicine] Strategic Program Lead, Strategy & Operations Dept., Commercial Excellence Strategic Program Lead for Johnson & Johnson Innovative Medicine Japan, focusing on evolving commercialization strategy, leading key initiatives, and introducing new capabilities. The role requires strategic thinking, project management, and stakeholder engagement, with a strong plus for AI experience in pharma. | — | 0 |
| Director, Head of Value, Evidence & Access This role leads the Value, Evidence & Access (VE&A) team within Johnson & Johnson Innovative Medicine Japan, focusing on driving Japan's Health Technology Assessment (HTA) preparation, submission, and negotiation. It involves building market access evidence generation strategies, collaborating with cross-functional teams, managing budgets, and leading a team. The role requires a deep understanding of the Japanese healthcare system and health economics. | — | 0 |
| [Innovative Medicine] メディカルアフェアーズ本部 イムノロジー･肺高血圧症･ニポカリマブ部門 ポートフォリオ部 ポートフォリオメディカルサイエンスリエゾングループ メディカルサイエンスリエゾンートフォリオ部 ポートフォリオメディカルサイエンスリエゾングループ メディカルサイエンスリエゾン Johnson & Johnson is seeking a Medical Science Liaison (MSL) for their Innovative Medicine division in Tokyo, Japan. This role involves building relationships with Key Individuals (KIs) in the immunology, pulmonary hypertension, and nipocalimab therapeutic areas, implementing medical plans through scientific communication, and gathering insights on unmet medical needs. Responsibilities include leading projects, analyzing findings for strategic input, and contributing to the development of junior MSLs. The role requires business-level Japanese and English, strategic agility, deep therapeutic area and product knowledge, and strong scientific communication and external engagement skills. | — | 0 |
| [Innovative Medicine] Staff, Quality Control Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant) Staff position in Quality Control Group at Johnson & Johnson's Innovative Medicine division in Japan. The role focuses on implementing, improving, and harmonizing laboratory quality systems in compliance with GMP/GCTP and J&J guidelines. Responsibilities include leading the transfer of analytical methods, overseeing QC activities for new product launches, ensuring system compliance for regulatory filings, managing stability programs, and supporting projects to improve efficiency and reduce costs. Requires a Bachelor's degree in a science field, 3+ years of pharmaceutical industry experience, and experience in GMP-compliant lab systems. | — | 0 |
| [Innovative Medicine] 生産物流本部 DELIVER JAPAN ディストリビューションセンター 東日本物流センター スタッフ This role is for a Distribution Center Staff position at Johnson & Johnson's Innovative Medicine division in Misato, Saitama, Japan. The primary responsibilities include managing the storage, receipt, and shipment of pharmaceutical products, handling inquiries, ensuring compliance with regulations like the Pharmaceutical and Medical Device Act, managing outsourced vendors, and participating in process improvement projects. The role requires strong communication, problem-solving, and compliance awareness, with experience in supply chain or the pharmaceutical/drug wholesale industry being essential. | — | 0 |
| [Quality] 信頼性保証部 カスタマーリレーションズ TSR (Telephone Service Representative)(契約社員) This role is a Telephone Service Representative in the Quality Assurance department, focusing on customer relations for the Vision Care Company. The primary responsibility is to receive, collect, and record customer complaints and quality information from the market using a global application with AI assistance. The role involves information gathering, data entry into a database, and collaborating with safety management for medical complaints. It requires customer service experience, PC skills, and strong communication abilities, with a focus on providing optimal solutions within legal and company regulations. | — | 0 |
| [Medtech] Quality Operations Staff, Quality Control (Sukagawa) Quality Operations Staff, Quality Control role at Johnson & Johnson's MedTech division in Sukagawa, Japan. Responsibilities include managing incoming inspections and processes for active medical devices, overseeing external inspection vendors, coordinating with domestic and international teams, participating in new product introduction projects, and preparing for quality audits. Requires experience in manufacturing, QA/QC, GMP, ISO13485/ISO9001, and strong English communication skills. | — | 0 |
| [Quality] QA Specialist, Quality Systems [MedTech] The role is responsible for maintaining Johnson & Johnson's Quality Management Systems (QMS) in Japan, ensuring compliance with Japanese regulations and J&J Quality Policies. This includes managing quality metrics, improving procedures, training employees, conducting internal and external audits, and managing business licenses. The role acts as a 'Process Owner' for specific QMS elements, focusing on non-conformance/corrective action (NC/CAPA), internal audits, and management reviews. | — | 0 |
| [Quality] QA Specialist, Quality Systems [MedTech] This role is responsible for maintaining Johnson & Johnson's Quality Management Systems (QMS) in Japan, ensuring compliance with Japanese regulations and J&J Quality Policies. Key responsibilities include analyzing quality metrics, improving procedures, conducting internal and external audits, managing business licenses, and acting as a Process Owner for Quality Systems elements. The role requires excellent Japanese communication skills for interacting with auditors and government officials, logical thinking, and good English communication. | — | 0 |
| ［MedTech］Data Strategy & Architecture Manager, Strategy & Commercial Excellence, Orthopedics Manager, Data Strategy & Architecture role at Johnson & Johnson (DePuy Synthes) focused on leading the development of data infrastructure in Japan, aligning with global digital strategy. Responsibilities include data governance, quality improvement, and designing data architecture across multiple systems (CRM, ERP, DWH). Collaborates with commercial, IT, and global teams to enable data-driven decision-making and business improvements. | — | 0 |
| ［MedTech］Demand Planning, Integrated Supply Chain, Surgery & Cardio Plan The IBP Planner role is responsible for demand planning and inventory/supply management within Johnson & Johnson's MedTech division. This position involves developing and communicating a consensus forecast by integrating historical data, market data, and strategic plans through collaboration with sales, marketing, finance, and supply chain partners. Key responsibilities include managing supply and inventory to maintain high service levels while optimizing inventory, creating scenario plans for new product launches, mitigating supply shortages, and meeting KPI targets. | — | 0 |
| [MedTech] Consumable Plan Specialist, Integrated Supply Chain This role is responsible for demand and inventory planning for the consumable portfolio in Japan, partnering with various departments to create accurate demand plans, support the IBP/S&OP process, manage inventory risks, and drive improvements in forecast accuracy. It involves generating statistical forecasts, consolidating commercial inputs, supporting S&OP activities, forecasting consumption tied to installed base, managing inventory risks, supporting launch planning, performing root-cause analysis on forecast variance, producing reports, improving planning efficiency through automation, and engaging with distributors and hospital procurement teams. The role also ensures compliance with regulatory, quality, and product safety requirements. | — | 0 |
| [Innovative Medicine] R&D, Senior Manager, Regulatory Strategy & Liaison Group, Regulatory Development, Regulatory Affairs Senior Manager, Regulatory Strategy & Liaison Group, Regulatory Development, Regulatory Affairs at Johnson & Johnson in Tokyo, Japan. This role provides strategic regulatory leadership, supports Regulatory Compound Leaders (RCLs), and contributes to cross-compound regulatory excellence. Responsibilities include leading and coordinating regulatory activities, providing strategic advice, managing NDA timelines, collaborating on early asset evaluation, and contributing to organizational development. Requires a bachelor's degree in a life-science or health-related discipline with at least 8 years of experience in R&D in the pharmaceutical industry (including 2+ years of regulatory experience) or health authorities. Must have experience with Japanese regulations and excellent communication skills in Japanese and English. | — | 0 |
| [Communication] Senior Manager, Core Capabilities HUB Japan [IM] Senior Manager, Core Capabilities HUB, Japan is accountable for leading the Japan implementation of the CPA HUB model, ensuring strategic consistency, operational excellence, and measurable impact. This role deploys, integrates, and optimizes core CPA capabilities in alignment with Global HUB strategy and standards, partnering with local teams to drive commercial impact and reputation outcomes. The role also ensures compliance, operational excellence, and agile execution, acting as a liaison between Japan and Global HUB. | — | 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 |
| [Innovative Medicine] Manager, Supply Chain Compliance and Business Excellence, Stable Supply System Management Office, Japan Supply Chain, Manufacturing and Supply Div. Manager role focused on supply chain compliance, inventory management, demand planning, and long-range capacity planning within Johnson & Johnson's Innovative Medicine division in Japan. The role ensures compliance with Japanese regulations, optimizes inventory, harmonizes demand planning, and supports strategic initiatives for stable supply. | — | 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 |
| [Innovative Medicine] R&D, Group Manager(Sr. Principal Scientist), Pharmacokinetics & Drug Metabolism, Preclinical Science &Translational Safety Japan This role focuses on non-clinical studies to support drug development in Japan, ensuring compliance with Japanese regulatory requirements and contributing to the scientific quality of non-clinical submissions for clinical studies and NDAs. It involves managing and coaching a group of scientists, planning group strategy, and aligning with international standards through external activities. The role requires expert knowledge of non-clinical areas and Japanese/EU/US regulatory guidelines, with over 12 years of experience. | — | 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 |
| [Innovative Medicine] Experienced Specialist, Risk Management Hematology, Local Medical Safety This role focuses on product safety and pharmacovigilance within the pharmaceutical industry, specifically managing risk management activities for J&J's Innovative Medicine portfolio in Japan. The individual will ensure compliance with local regulations and company policies, prepare and submit aggregate reports, and collaborate with cross-functional teams and health authorities. The role requires strong analytical, communication, and leadership skills, with fluency in both Japanese and English. | — | 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 |
| [HR] Talent Acquisition Contract/契約社員 [MedTech] This is a Talent Acquisition role at Johnson & Johnson's MedTech division in Tokyo, Japan. The role focuses on sourcing and managing the end-to-end recruitment process for sales and other positions. It requires direct sourcing experience, strong administrative skills, proficiency in MS Office and Workday, and the ability to analyze recruitment data. Fluency in Japanese is essential, with English proficiency preferred for reading emails and system interfaces. The role involves collaboration with hiring managers and HRBPs, candidate assessment, offer management, and ensuring a smooth onboarding process. | — | 0 |
| [IT] Order to Cash (O2C) Product Manager-Contract/契約社員 [Shockwave] Product Manager for Oracle Order to Cash (O2C) functionalities, focusing on design, implementation, and support of Order Management & Invoicing within Oracle Cloud ERP. Requires experience with Oracle Cloud implementations, specifically in Order Management, Billing, Account Receivable, Customer Master Data, and Pricing. Must also have knowledge of integrating Oracle Cloud with CRM applications like Salesforce and collaborate with Salesforce IT teams. The role involves translating business needs into scalable solutions, working with customer service and finance stakeholders, managing integrations with 3PL partners, and ensuring continuous system improvement. | — | 0 |
| [Innovative Medicine] Analyst, Operational Quality Group, Quality Operations Dept., Manufacturing and Supply Div. (Fuji Plant) This role supports manufacturing operations from a quality perspective, ensuring compliance with GMP/GCTP, safety, and corporate policies. Responsibilities include supporting and overseeing operations, addressing manufacturing issues, facilitating process improvements, supporting regulatory inspections, and making batch release decisions. The role also involves creating/updating procedures, completing training, and promoting quality culture. | — | 0 |
| [Quality] Senior Manager Commercial Quality [IM] Senior Manager/Director of Commercial Quality for Johnson & Johnson in Japan, serving as the Japan Quality Leader. Responsible for ensuring post-marketing GxP activities comply with Japan GQP, J&J global quality policies, and MAH requirements. The role also fulfills legal responsibilities of Marketing Supervisor General under the PMD Act, overseeing market quality surveillance and regulatory compliance for pharmaceuticals and regenerative products. Key responsibilities include QMS governance, GxP compliance, market quality surveillance, MAH accountability, and cross-functional leadership. | — | 0 |
| [Innovative Medicine] Associate Director, Patient Experience, Strategy & Operations Dept., Commercial Excellence This role focuses on building and leading patient experience strategies and operations within Johnson & Johnson's Innovative Medicine division in Japan. It involves leveraging technology and insights to optimize the patient journey, improve patient outcomes, and ensure compliance, quality, and patient safety. The role requires strategic thinking, change leadership, and people leadership to drive a data-driven culture and deliver best-in-class patient experiences. | — | 0 |
| [Innovative Medicine] Associate Director, Sales Force Effectiveness Group, Workforce Excellence Dept., Commercial Excellence The Associate Director of Sales Force Effectiveness Group will lead the planning and execution of SFE strategies, focusing on customer targeting, resource optimization, and incentive design to maximize the value generated by the sales force. This role involves managing a team, collaborating with diverse stakeholders, and contributing to organizational capability enhancement. The position requires experience in strategy development and execution within sales planning, data analysis, or marketing, preferably in the healthcare industry. | — | 0 |
| [MedTech] Service Performance Sr Manager, Service Innovation Johnson & Johnson MedTech is seeking a Service Performance Sr Manager, Service Innovation to support the Service organization in Japan. This role involves establishing collaboration between Japan and USA Service organizations, developing service processes and infrastructure, and contributing to the Service product roadmap. The position requires experience in DFX, designing for Serviceability, and understanding of product creation processes within a regulated environment. | — | 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 |
| [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 |
| [Communications} Communications and Public Affairs Contract/契約社員 [IM] This role is for a Communications and Public Affairs professional within the Immunology, PAH, and Neuroscience (IPN) Business Unit at Johnson & Johnson's Janssen Japan. The primary focus is on developing and executing communication strategies to increase disease awareness, improve patient access to medicines, and build the company's reputation in the IPN space. The role also involves driving employee engagement, managing external partners and budgets, and providing strategic communication counsel to leadership. | — | 0 |
| [Innovative Medicine] Associate Director, Government Affairs and Policy Dept., Integrated Market Access Div. Associate Director/Senior Manager for Government Affairs and Policy in Innovative Medicine, focusing on shaping policy to improve patient access to innovative medicines in Japan. Requires strong communication skills in Japanese and English, deep knowledge of the healthcare industry, and experience in policy development and stakeholder engagement. | — | 0 |
| [Innovative Medicine] Senior Manager, Oncology, Clinical Science Senior Manager, Oncology, Clinical Science role at Johnson & Johnson Innovative Medicine R&D, focusing on providing Japanese clinical insights and expertise to develop global clinical development strategies. Responsibilities include overseeing clinical studies, leading regulatory interactions with PMDA/MHLW, and mentoring junior scientists. The role operates within a matrix team and collaborates with global counterparts. | — | 0 |
| [Innovative Medicine] Capability Development Specialist/Manager, Capability & Digital Excellence Group, Medical Affairs This role focuses on developing capabilities and digital excellence within Medical Affairs at Johnson & Johnson. It involves managing the implementation of capability initiatives, designing and delivering programs, exploring future trends and digital advances, managing vendors, tracking budgets, and leading continuous improvement efforts. The role requires experience in process/capability management within regulated industries and a strong understanding of Medical Affairs processes. | — | 0 |
| [Vision Care] Executive Assistant, Marketing Executive Assistant role supporting the Head of Marketing and Marketing organization within Johnson & Johnson's Vision Care division in Tokyo, Japan. Responsibilities include managing complex schedules, coordinating meetings and travel, handling confidential information, supporting departmental operations, and assisting with company-wide events and onboarding. Requires a minimum of 5 years of experience as an Executive Assistant, strong organizational and communication skills in Japanese and English, and advanced proficiency in Microsoft Office. | — | 0 |