Manage and facilitate Project Osprey and Working Group meetings across JJMHK supply chain and be key conduit into EY consultant workstreams and PMO. Understand and familiarize current JJMHK DPS operation for overall supply chain and prepare for all future UAT test for internal and external partners. Develop a project management plan, integrated project schedule, reporting and related project management artefacts. Partner with business sponsors to define success metrics and criteria. Facilitate all operational checkpoint activities throughout the lifecycle of projects. Assess and resolve all high priority project risks as they are encountered, especially for the EDI connection with government. Ensure all projects adhere to project methodology compliance standards set by the company. Continually update relevant business stakeholders of project status and periodically publish project status reports. Represent the project in various project governance and inter-departmental forums. Define and track project milestones while developing, maintaining, and reporting on an overall integrated delivery plan. Ensure all projects meet success parameters and outcome targets stated in business case. Monitoring of and reporting on work schedules to ensure completion of work within time and budget constraints. Consider stranded cost opportunities to optimize DPS future operation.

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.

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.

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.

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.

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.

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.

Seeking a Senior Scientist with expertise in viral vectors and molecular biology to contribute to CAR-T cell therapy discovery efforts. Responsibilities include viral vector generation, testing, optimization, and analytical quantification, as well as assay development and collaboration with cross-functional teams.

Seeking a Senior Scientist with expertise in viral vectors and molecular biology to join CAR-T cell therapy discovery efforts. Responsibilities include designing, modifying, and optimizing viral envelopes/proteins, establishing experimental workflows, and supporting the development of analytical assays. The role requires a Ph.D. or Master's/Bachelor's with extensive experience in enveloped viruses and viral vector engineering.

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.

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.

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.

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.

Staff R&D Scientist role focused on the design, development, and testing of intraocular lenses and optical metrology. Responsibilities include ideation, requirements development, protocol execution, IP strategy, and leading research teams. Requires a PhD in Optics, Physics, Vision Science, or Mechanical Modelling, with proficiency in optical design tools like Zemax.

Senior Analyst for SAP Finance Product Costing at Johnson & Johnson, focusing on Supply Chain Finance business processes and SAP-ERP technical capabilities. Requires experience in Pharmaceuticals/Healthcare industry and knowledge of SOX & GxP compliance. Experience with Agile methodology and SDLC is also required.

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.

Senior Manager/Associate Director of Regulatory Affairs for Hematology & Oncology Early Development in China, responsible for end-to-end regulatory strategy, submissions, approvals, and lifecycle management, liaising with regulatory agencies and cross-functional teams.

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.

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.

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.

Johnson & Johnson is seeking a Director, Search & Evaluation for their External Scientific Innovation (ESI) team in Tokyo, Japan. This role focuses on identifying and evaluating external innovation opportunities in the life sciences ecosystem across the Asia Pacific region, with a primary focus on Japan. The Director will build relationships with academia, venture capital, and startups to source and advance potential pipeline opportunities, acting as a key liaison between external partners and internal J&J teams.

The Scientific Advisor role is a member of the Medical Affairs Department and plays a major role in providing expert scientific advice on branding and strategic development within assigned therapeutic areas. This individual facilitates pipeline product introduction and on-market product access by developing scientific relationships with external stakeholders and collaborating with all internal stakeholders to develop and implement the overall medical strategy in alignment with therapeutic brand strategy as well as company strategy. The Scientific Advisor is responsible for the implementation of all related medical affairs activities including KOL development, scientific communication, medical education, data generation, pre-approval access, unsolicited medical information, review and approval of promotional materials, and internal training.

This role is for a Regulatory Affairs Staff position within the MedTech sector at Johnson & Johnson, focusing on Orthopaedics Trauma/PT. The primary responsibilities involve planning, preparing, and executing regulatory actions to support business goals, building regulatory strategies for new product introductions, liaising with regulatory bodies like PMDA for approvals, and managing post-market changes in compliance with laws and regulations. The role also includes advertising review and handling inquiries. A minimum of 5 years of experience in medical device regulatory affairs (Class II or above) is required, along with English proficiency for understanding design documents and communicating with overseas stakeholders.

This role drives manufacturing innovations in the Joints Supply Chain, focusing on translating site needs into engineering tasks, designing and delivering technical solutions, and contributing to the site's innovation roadmap and KPIs. The engineer will support projects from design through commissioning, collaborating across functions and ensuring improvements in machine utilization and line performance.

Sustaining Engineer for Product Lifecycle in MedTech Cardiovascular, focusing on hardware development and manufacturing support for released systems. Responsibilities include developing hardware solutions, writing production procedures, designing tools, solving technical issues, improving production yield, conducting failure analysis, and communicating with R&D.

Operates manufacturing equipment to assemble, test, and inspect medical devices according to documented procedures. Records batch history, maintains clean workstations, and ensures product quality and traceability. Follows GMP and GDP standards.

Production Supervisor role at Johnson & Johnson in Suzhou, China, focusing on manufacturing operations, quality, safety, and continuous improvement within a supply chain context. The role involves leading production staff, ensuring adherence to policies and regulations, managing resources, and supporting projects and process improvements. It is a people leader position with responsibilities in operational efficiency and compliance.

The Medical Device Assembler role at Johnson & Johnson focuses on assembling, inspecting, and testing high-quality medical devices in a controlled manufacturing environment. This position requires experience with microscope-based assembly, manual dexterity, and adherence to strict quality and regulatory standards within the healthcare industry.

This role focuses on leading Japanese regulatory strategy and submissions for new drug development within Johnson & Johnson's Innovative Medicine division. It involves preparing dossiers for submission to Japanese Health Authorities (HA), responding to HA questions, and developing target labeling. The position requires close collaboration with global regulatory teams and project teams to ensure compliance and successful registration of products in Japan.

Software Engineer role at Johnson & Johnson MedTech Cardiovascular in Yokneam, Israel. The role involves developing innovative software solutions in C++ and C# for cutting-edge diagnostic medical device products, focusing on designing and implementing SW components and algorithms for multi-threaded systems.

Apprenticeship position for a Kaufmann:frau EFZ (Business Administrator) in the healthcare industry, focusing on administrative and organizational tasks within a global network and innovative projects.

Sr. Design Quality Engineer responsible for ensuring hardware and embedded software designs for medical devices comply with regulations, standards, and internal procedures. This includes developing and reviewing V&V test plans, risk management, and supporting regulatory submissions and manufacturing quality.

The Senior Manager/Associate Director Strategic Account Lead (SAL) is responsible for uncovering new opportunities and fostering mutually beneficial transformations with strategic partners to increase value in clinical research. This role involves optimizing clinical trial delivery, building commitment between Janssen and strategic accounts, and managing key internal and external stakeholder relationships. The SAL will contribute to company strategy, analyze market dynamics, develop account-specific plans, and integrate R&D strategies to enhance clinical trial delivery outcomes. The role requires a strong understanding of clinical operations, market trends, and the ability to lead cross-functional teams.

Internship program focused on evaluating the impact of post-treatment on survival in pivotal cancer trials. Responsibilities include literature review, methodology summarization, scenario setting, and implementing simulation programs using R or SAS. The role involves collaboration with internal departments and contributing to clinical development. Research outcomes belong to J&J IM.

Manager Quality Assurance role at Johnson & Johnson in Tokyo, Japan. Responsible for maintaining the Quality Management System (QMS) in compliance with MHLW ordinance No 169 and other regulatory requirements. This includes establishing and maintaining QMS procedures, identifying changes to regulatory requirements, conducting gap assessments, training the organization, managing the NCR process, and overseeing supplier management and audits. Requires a BS degree with 10+ years of experience in medical device quality systems and compliance, and 2 years of managerial experience.

This role focuses on applying clinical pharmacology knowledge, including PK/PD analyses and model-based drug development principles, to drug development programs in Japan. Responsibilities include designing clinical studies, conducting PK/PD analyses, integrating data, preparing regulatory submissions (Japan NDA), and responding to regulatory queries. The role requires collaboration with global teams and adherence to regulatory guidelines.

This is a job posting for individuals with disabilities in Japan, seeking candidates for various assistant roles within the Johnson & Johnson Japan Group. The roles include sales, marketing, HR, accounting, IT, and general departmental assistants. The posting emphasizes stable attendance, self-management of health, accurate task execution, independent prioritization, and requires at least two years of general administrative experience, communication skills, and intermediate PC skills. It is not an AI-related role.

Operador de Manufactura I at Johnson & Johnson MedTech in Grecia, Costa Rica. This role supports the Epsilon program and operational readiness for new manufacturing plants. Responsibilities include assisting in the installation, operation, maintenance, and troubleshooting of machinery and equipment, supporting product component installation, and ensuring quality specifications are met. The role involves operating and maintaining assembly and packaging equipment, maintaining production records, and adhering to GMP, GDP, and safety standards.

This role is for a Warehouse position at Johnson & Johnson's Fuji plant in Japan. The primary responsibilities include executing warehouse operations according to company rules and SOPs, managing contractors, ensuring safe operation of equipment like forklifts and automated cranes, suggesting improvements for efficiency, conducting training to comply with GMP, reporting deviations and quality issues, performing 5S actions, coordinating with the support group for smooth delivery, executing sampling tasks accurately, and conducting safety training for drivers. The role also involves managing the handling, storage, and records for narcotic products in compliance with regulations.

Johnson & Johnson is seeking a Business Operations & Strategy Group Manager/Sr. Manager for their Fuji Plant in Shizuoka, Japan. This role involves guiding the site's direction, shaping strategy, driving outcomes, and managing strategic initiatives. The position requires a strong understanding of supply chain in a regulated manufacturing industry, business and financial acumen, and leadership skills. The role also involves risk management, stakeholder communication, and team management.

The Senior Manager/Director of Commercial Quality will lead post-marketing GxP activities in Japan, ensuring compliance with GQP, J&J global quality policies, and MAH requirements. This role also fulfills legal responsibilities as a Marketing Supervisor General under the PMD Act, overseeing market quality surveillance, complaint handling, regulatory reporting, and product recalls. The position requires a deep understanding of pharmaceutical quality systems, regulatory compliance, and people leadership, with a focus on patient safety and business continuity.

Johnson & Johnson is seeking a Senior Systems Test Engineer for their DePuy Synthes team in Palm Beach Gardens, Florida. This role involves contributing to the research, design characterization, verification, and risk assessment of medical implants and instrumentations for mechanical and electro-mechanical applications. The engineer will develop and ensure testability of requirements, create test methods to verify safety and efficacy, and lead verification testing efforts. The role requires experience with electromechanical test equipment, lab instrumentation, and working in a regulated medical device industry.

This role is for a Senior Principal Scientist in Pharmacology at Johnson & Johnson's Innovative Medicine division. The primary focus is on non-clinical submissions for regulatory approval in Japan, integrating data from toxicology, safety pharmacology, and DMPK. The scientist will prepare and review non-clinical sections of regulatory documents, collaborate with internal and external experts, and ensure compliance with Japanese regulatory requirements. While AI is mentioned as a modern approach to prepare documents, the core function is not AI/ML development but rather regulatory science and data integration in the pharmaceutical domain.

Internship position for pharmacists (m/w/d) in Neuss, Germany, focusing on gaining experience in various pharmaceutical and healthcare-related areas within Johnson & Johnson. Opportunities include Commercial Quality, Global Clinical Operations, Medical Information & Communication, Immunology, and Pharmacovigilance. The role involves supporting project managers, evaluating complaints, handling customer inquiries, and contributing to departmental projects.

Senior Director, Medical Affairs for IPN (Immunology/Pulmonary Hypertension/Neuroscience) in Japan. This role leads a team responsible for medical strategy development, execution of medical and scientific activities, and collaboration with internal and external stakeholders. The position requires deep insight into therapeutic areas, knowledge of the Japan market, and people management experience. The role ensures compliance with Japan Legislation and HCC rules.

This role is responsible for GVP (Good Vigilance Practice) activities, including handling complaints and reporting adverse events to the competent authority in Japan. It involves collaborating with US headquarters, maintaining documentation, and ensuring compliance with Japanese regulations like PMDA Act and QMS Ordinance. The role requires experience in the medical industry, knowledge of GVP, and English reading/writing skills.

This role is for a Regulatory Affairs Leader in the Orthopaedics business unit within Johnson & Johnson MedTech. The primary responsibilities include planning, preparing, and executing regulatory actions for medical devices, building regulatory strategies for new product introductions, negotiating with regulatory bodies like PMDA, and managing post-market changes to ensure stable supply. The role requires at least 5 years of experience in medical device regulatory affairs (Class II or above) and proficiency in English for communication with overseas manufacturers and internal stakeholders.

This is an internship role at Johnson & Johnson focused on operating and maintaining CNC machinery in a manufacturing environment. Responsibilities include ensuring machine efficiency, adhering to quality standards, modifying machine settings under guidance, operating auxiliary equipment, downloading CNC programs, and maintaining traceability. The role emphasizes safe and effective operation of manufacturing equipment.