Currently tracking 49 active AI roles, down 47% 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.
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 57 new AI-related roles. That is a -46% change versus the prior 30 days (106 → 57).
| Title | Stage | AI score |
|---|---|---|
| Technical Product Manager, Patient Experience Technical Product Manager for patient experience solutions in APAC, focusing on digital portals, CRM, and data platforms. The role involves product strategy, roadmap, delivery, and ensuring compliance with healthcare regulations. | — | 0 |
| Complaints Team Leader Johnson & Johnson is seeking a Complaints Team Leader in Yokneam, Israel, to lead a team responsible for product complaint investigations, trending, and signal detection within the Quality Assurance organization. This role requires ensuring timely and compliant complaint handling, collaborating with cross-functional teams, and driving process improvements in a regulated medical device environment. | — | 0 |
| Exp Anlst Quality Assurance Johnson & Johnson is seeking a QA Investigations Associate for their CAR-T hub in Ghent, Belgium. The role involves managing deviations, non-conformances, and implementing corrective and preventive actions (CAPAs) to ensure product and process quality in CAR-T manufacturing, adhering to ATMP/GMP requirements. |
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| Marketing Intern Marketing Intern at Johnson & Johnson supporting the execution of marketing activities for the Neuroscience portfolio, including material approval, monitoring utilization, developing CLM materials, market research, and tracking brand performance. Requires enrollment in Business Administration/Economics, marketing enthusiasm, and strong communication skills in English and Turkish. | — | 0 |
| Medical Affairs Lead - Haematology Medical Affairs Lead role for Haematology portfolio in ANZ, responsible for shaping strategy, leading a team, engaging stakeholders, and ensuring compliant execution of Medical Affairs activities. Requires advanced degree, pharmaceutical industry experience, and people leadership skills. | — | 0 |
| Business Operations Specialist This role is for a Business Operations Specialist at Johnson & Johnson in Sweden, focusing on the planning, coordination, and execution of customer events across various therapeutic areas. The specialist will manage event logistics, administration, documentation, vendor coordination, and ensure compliance with J&J policies and external regulations. The role requires strong organizational and stakeholder management skills, with an interest in leveraging digital tools and AI for operational efficiency. | — | 0 |
| Medical Governance Manager This role is for a Medical Governance Manager at Johnson & Johnson, focusing on implementing and maintaining the ABPI compliance framework in the UK. The manager will act as an ABPI signatory, review and certify materials, update SOPs, develop compliance training, lead monitoring activities, provide advice on code interpretation, manage risk assessments, and maintain records. The role requires experience with the ABPI Code of Practice and the ability to register as a signatory, with a background in medical affairs or medical information. | — | 0 |
| PharmD Fellow Safety Analysis Scientist This role is a PharmD Fellow position focused on safety analysis and risk management within Johnson & Johnson's Innovative Medicine division. The fellow will prepare scientific safety analyses and evaluations for regulatory compliance and decision-making, support safety management teams, and gain experience in case processing and signal management. The role emphasizes collaboration, data analysis, and report writing in a healthcare/pharmaceutical context. | — | 0 |
| Director Compliance Principal Johnson & Johnson is seeking a Director Compliance Principal for their Med-Tech JJRC Team. This role provides tactical and strategic compliance support, ensuring regulatory standards are met. Responsibilities include leading follow-up activities for audits, assessments, inspections, and health authority actions, as well as identifying, escalating, and mitigating risks. The position requires expertise in global regulatory compliance within the medical device/biotech/pharmaceutical industry and experience with Quality System regulations and GXP audits. | — | 0 |
| Medical Science Liaison - GU Oncology - (MN/SD/ND) This role is for a Medical Science Liaison in GU Oncology for Johnson & Johnson Innovative Medicine. The primary focus is on building relationships with Key thought leaders/HCPs, providing scientific and clinical information, and generating insights within the assigned territory. While the role mentions leveraging AI tools, it is not the core craft, and the primary responsibilities are related to medical affairs and scientific exchange in the healthcare domain. | — | 0 |
| Product Development Engineer Product Development Engineer role at Johnson & Johnson focused on the design and development of orthopaedic medical devices. The role involves working on cross-functional teams through all phases of the product life-cycle, from concept to commercialization and post-market surveillance. Responsibilities include leading design projects, defining user needs, solving design problems using CAD and prototyping, developing layouts and tolerance studies, executing design verification/validation plans, supporting regulatory processes (MDR, FDA Design Control, 510(k)), optimizing designs for manufacturability, and performing complaint investigations. Requires a BS/MS in Mechanical or Biomedical Engineering and strong communication skills. | — | 0 |
| Site Engineering Lead Site Engineering Lead at Johnson & Johnson's Innovative Medicine division in Cork, Ireland. This role focuses on leading engineering and technology solutions, maintenance, and automation to support API manufacturing. Responsibilities include budget management, team development, implementing standards, risk assessment, and project execution within a regulated healthcare environment. | — | 0 |
| Engineer I, Source Quality, Orthopedics This role is for an Engineer I in Source Quality within the Orthopedics division, focusing on managing external manufacturers and suppliers. Responsibilities include establishing quality expectations, implementing process controls, supporting product launches, conducting supplier visits, providing quality engineering support for non-conformances and validation, contributing to root cause investigations, and applying risk management tools. The role requires a Bachelor's degree in Engineering or a related scientific field and 0-2 years of experience. Preferred qualifications include experience in manufacturing processes, the medical device industry, Six Sigma/Lean, quality engineering, blueprint reading, FDA CFR Part 820, ISO 13485, and process validation. | — | 0 |
| Process Engineering Process Engineer at Johnson & Johnson's Vision division in Groningen, Netherlands, focusing on manufacturing intraocular lenses. The role involves leading process engineering projects, continuous improvement initiatives, characterization, and NPI changes. Responsibilities include identifying opportunities for process enhancements, designing experimental protocols, analyzing production data, leading Six Sigma initiatives, and supporting new product introductions within a GMP and ISO compliant environment. Requires a Bachelor's or Master's degree in Engineering or Material Science with relevant experience, and project management skills. Experience in an FDA-regulated environment and Six Sigma certification are preferred. | — | 0 |
| MSL Medical Science Liaison (Oncology) responsible for discussing products, patient treatment trends, and studies with leading specialists, acting as a scientific expert and trusted counterpart. The role involves developing and maintaining relationships with key opinion leaders, communicating scientific data, supporting medical education, and providing scientific support to commercial teams. It also includes managing clinical activities, supporting registries, RWE studies, and investigator-initiated studies, while ensuring compliance and ethical behavior. | — | 0 |
| Director, Service & Repair Quality Johnson & Johnson is seeking a Director, Service & Repair Quality to lead continuous quality improvements and maintain compliance for medical device service and repair operations across global sites. The role involves talent acquisition, ensuring awareness of regulatory requirements, auditing the quality system, applying FDA and international regulatory knowledge, developing sampling plans, performing data analysis, designing risk management programs, and leading compliance support during inspections. Requires a Bachelor's degree in Science or Engineering and a minimum of 10 years of GMP-related experience in a Med Device or biotech manufacturing facility with serviceable devices, including 7 years of leadership experience in Quality with serviceable devices and teams. | — | 0 |
| Director, Service & Repair Quality Director of Service & Repair Quality for medical devices at Johnson & Johnson, focusing on continuous quality improvements, regulatory compliance, and global multi-site support. Requires extensive experience in GMP and leading quality teams in a MedTech manufacturing environment. | — | 0 |
| Associate Manufacturing Engineer Associate Manufacturing Engineer role focused on ensuring reliable production, driving continuous improvement, and supporting the introduction of new technologies in a healthcare manufacturing environment. Responsibilities include process and equipment validation, contributing to improvement initiatives using Lean and Six Sigma, data collection, documentation, and troubleshooting. | — | 0 |
| Regional Franchise Planner The Regional Franchise Planner is responsible for demand and deployment planning for the Medical business in the EMEA region, collaborating with global and country supply chain teams to achieve business goals. This role involves providing statistical forecast input, coordinating demand-supply handovers, ensuring product availability, managing inventory, and operating planning systems. | — | 0 |
| Senior Planner- External Operations This role is for a Senior Planner in External Operations at Johnson & Johnson, focusing on supply chain planning for medical devices. Responsibilities include leading S&OP meetings with external suppliers, planning and controlling finished goods inventory, analyzing inventory levels and forecasts, implementing strategies to improve customer service and operational metrics, developing planning scenarios, and leading digital projects for process and data management. The role also involves overseeing planning and execution management of complex medical device supply chains, monitoring supplier KPIs, developing purchase plans, translating demand forecasts into SKU level plans, optimizing external operations planning, maintaining supplier relationships, developing inventory policies, coordinating shipments, reporting supply shortages/surpluses, and placing purchase orders. Experience with SAP S4/Hana or similar ERP systems is preferred, along with strong analytical skills and advanced Excel knowledge. Experience in the Medical Device industry is also a plus. | — | 0 |
| Director Government Affairs & Access Policy Director Government Affairs & Access Policy for Johnson & Johnson Innovative Medicine in Germany. This role involves leading the GA&AP team, developing and implementing strategy, managing patient engagement, monitoring the external environment, analyzing policy fields, managing strategic planning, handling issue and crisis management, leading the team, and representing J&J externally. It requires close collaboration with various internal functions and external stakeholders, including political decision-makers and patient organizations. The role also involves building and maintaining networks, leading engagement in industry associations, and contributing to EU-level discussions. | — | 0 |
| RA Professional Labeling EUCP (12-month contract) This role is for a Regulatory Affairs Professional focused on labeling for EU Product Information (EUPI) for products approved via the Centralized Procedure. Responsibilities include coordinating translation, linguistic review, and submission of EUPI changes, ensuring accuracy and compliance with EU guidance. The role requires at least 3 years of regulatory affairs experience with labeling documents and in-depth knowledge of European regulations, particularly EMA. | — | 0 |
| Transportation Analyst The Transportation Analyst role at Johnson & Johnson focuses on managing outbound transportation networks for finished goods, ensuring reliable, compliant, and cost-effective delivery. Responsibilities include coordinating shipment execution, managing carrier performance, handling exceptions, developing transportation metrics, supporting cost improvement programs, and ensuring regulatory compliance. The role requires analytical skills, experience in transportation or logistics, and proficiency in Microsoft Office. | — | 0 |
| RA Professional Labeling EUCP (12-month contract) This role coordinates the translation, linguistic review, and submission of EU Product Information (EUPI) for products approved via the Centralized Procedure. It involves obtaining information on EUPI changes, managing external translation vendors, ensuring accuracy of translated documents against English source text, performing quality checks, and maintaining compliance in the company's repository system. The role requires at least 3 years of regulatory affairs experience with labeling documents and in-depth knowledge of European regulations (EMA). | — | 0 |
| JJT Cutover Lead E2E Johnson & Johnson Innovative Medicine is seeking a JJT Cutover Lead E2E in Bangalore, India. This role will lead the planning and execution of parallel cutovers for a global business transformation program modernizing ERP systems. The lead will develop cutover strategies, coordinate detailed plans, train teams, collaborate with system integrators, conduct testing, manage readiness, and drive issue resolution. The role also involves piloting new technologies like automation and generative AI to improve cutover efficiency and embracing industry best practices. | — | 0 |
| Sr Manager, Project Controls & Assurance This role is for a Sr Manager, Project Controls & Assurance at Johnson & Johnson, focusing on ensuring compliance with company procedures and implementing project controls tools and best practices throughout the project lifecycle. The responsibilities include managing cost and schedule metrics, risk management processes, early estimating, and supporting project delivery teams. The role requires full-time on-site support in Wilson, North Carolina. | — | 0 |
| Lead, QA Strategy Lead, QA Strategy for a global business transformation program modernizing foundational transactional processes and harmonizing them into one ERP system for Johnson & Johnson's Innovative Medicine division. This role is responsible for defining and owning the program-level QA strategy, Quality Plan, risk tolerance, acceptance criteria, and ensuring inspection readiness and alignment with program timelines. It involves driving risk management, business readiness, and system acceptance activities, acting as an independent quality voice, and ensuring compliance with GMP, GxP, 21 CFR Part 11, EU Annex 11, and data integrity expectations within a regulated pharmaceutical environment. | — | 0 |
| Senior Manager, Lab Automation and Screening Operations Senior Manager to lead laboratory automation, data management workflows, and screening operations at a healthcare research site. Focus on delivering reliable automated screening and compound profiling capabilities, advancing infrastructure, data integration, and operational excellence. | — | 0 |
| Global Supply Planner This role is for a Global Supply Planner at Johnson & Johnson, focusing on ensuring product availability and efficient supply across a global network. It involves translating demand and supply signals into executable plans, collaborating with various departments, balancing demand/inventory/capacity, managing master data, handling purchase orders, and performing ad-hoc analysis. The role requires experience in supply chain planning, ERP systems, and working in regulated industries. | — | 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 |
| QC Technology & Innovation Specialist This role focuses on identifying and implementing automation and simplification opportunities within a Quality Control (QC) laboratory at Johnson & Johnson. Key responsibilities include developing competencies in LIMS software for master data management to simplify analysis execution and data archiving, analyzing laboratory needs, and collaborating on project implementation. Other opportunities involve managing stability samples, consumables, and electronic laboratory systems. The role is primarily focused on process improvement and digital transformation within a regulated healthcare environment. | — | 0 |
| Senior Site Manager Senior Site Manager role in R&D Operations for Clinical Trial Support at Johnson & Johnson. This mid-level role (3-5 years experience) acts as the primary contact between the Sponsor and Investigational Sites, ensuring inspection readiness by adhering to protocols, SOPs, GCP, and regulations. Responsibilities include site selection, qualification, recruitment planning, initiation, monitoring (on-site and remote), and close-out activities. The role involves partnering with other trial management roles, contributing to process improvement, training, and mentoring, and operating independently. | — | 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 |
| MSL Johnson & Johnson is seeking a Medical Science Liaison (MSL) in Oncology, based in Breda, Netherlands. This role involves engaging with healthcare professionals to provide scientific information about products, executing the medical affairs tactical plan, and collaborating on clinical research and data dissemination. The ideal candidate has a scientific degree, experience in medical affairs within the pharmaceutical industry, and strong communication and analytical skills. | — | 0 |
| Process Engineer(Machining), Orthopedics This role provides technical assistance to engineers in the Orthopaedics business, focusing on process engineering tasks such as drafting drawings, developing CNC/Laser programs, maintaining SAP data, and supporting validation activities. It also involves assisting with quality systems and documentation in compliance with healthcare regulations. | — | 0 |
| Clinical Specialist - Upper Extremities & Sports Medicine, NSW/VIC/SA - Orthopaedics Clinical Specialist role in Orthopaedics, providing intraoperative support, surgical preparation, clinical education, technical expertise, and product management for sports medicine and extremities. Requires a health-related qualification and ability to travel and work on-call. | — | 0 |
| Qualified Person The Qualified Person provides QA support and oversight for Advanced Therapy (AT) products, including API (Lentiviral) manufacturing and QC testing, ensuring GMP compliance and product quality for commercial and clinical use. This role involves reviewing investigations, non-conformances, CAPAs, and participating in risk assessments and regulatory inspections. | — | 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 |
| Loan Kit Technician The Loan Kit Technician role at Johnson & Johnson MedTech is responsible for the inspection, assembly, dispatch, and receipt of orthopaedic loan sets. This involves managing kit movements within an ERP system, verifying cleanliness and functionality of returned kits, liaising with hospitals regarding instrument issues, supporting inventory management, and ensuring timely dispatch of kits. The role also requires adherence to quality management systems like ISO 13485 and participation in on-call duties. A background in MedTech, biomedical sciences, or orthopaedics is preferred, along with strong attention to detail and problem-solving skills. | — | 0 |
| Senior Site Manager Senior Site Manager for clinical trials at Johnson & Johnson, ensuring investigational sites comply with protocols, SOPs, GCP, and regulations from study start-up to closure. Responsibilities include site selection, initiation, monitoring, recruitment planning, supply management, data entry, query resolution, adverse event reporting, and documentation. The role partners with local and central trial teams, mentors junior staff, and may participate in process improvement and regulatory submissions. | — | 0 |
| Manager Technical Product Management Manager Technical Product Management at Johnson & Johnson, focusing on evolving the Pharmacovigilance (PV) technology landscape, specifically case processing systems and operational excellence. The role involves owning the product roadmap, leading Agile delivery, ensuring compliance with global PV regulations, and driving adoption of automation and AI. Requires experience with specific PV software (ArisGlobal LSMV, ReporterX, XDI, RxLogix) and GxP-regulated environments. | — | 0 |
| AIQ IT Lead This role is for a Technology Lead focused on qualifying and managing laboratory analytical instruments (AIQ) within a GxP-regulated environment at Johnson & Johnson. The role involves ensuring laboratory systems are compliant, secure, and meet data integrity standards, working with IT, Quality, and Engineering teams, and managing vendor relationships and technology projects. It is not directly involved in building or researching AI/ML models. | — | 0 |
| CNC Manufacturing Engineer This role executes engineering deliverables for large-scale manufacturing capacity projects, focusing on stable, reliable, and cost-effective processes. It involves supporting knowledge transfer and implementing best practices in collaboration with functional organizations. | — | 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 |
| Systems Integration Engineer Johnson & Johnson is seeking a Systems Integration Engineer with a focus on mechatronics systems for their J&J Robotics division. The role involves supporting the development and sustaining of robotic surgical subsystems, planning and implementing integration activities, analyzing and resolving integration issues, and developing new test methods. The position requires a BS or advanced degree in a relevant engineering field with 1-2+ years of experience, hands-on experience with electromechanical systems, and basic programming skills in Python/C++. | — | 0 |
| Sr Mgr, Q&C Strat & Org Engagement This role shapes and drives enterprise-wide enablement of the Quality & Compliance (Q&C) strategy, ensuring priorities are understood, owned, and operationalized across the organization. It involves partnering with leadership to orchestrate strategy activation, aligning forums, engagement mechanisms, and narratives to priority outcomes. The role also involves creating strategic content, leading organizational engagement, supporting leadership, and identifying efficiencies through new digital and AI solutions. | — | 0 |
| Director of Technical Transfer & Validation Director of Technical Transfer & Validation for a medical device business, responsible for leading engineering activities related to product lifecycle, process development, and technology solutions. This role ensures the development and execution of quality work for compliant medical device production and sustaining operations, collaborating with various departments to improve supply reliability, quality, efficiency, and innovation. | — | 0 |
| Robotics and Controls Engineer - Strategic Robotics Johnson & Johnson is seeking a Robotics and Controls Engineer to develop robotic solutions for next-generation medical robotic systems. The role involves designing and implementing software in a real-time, safety-critical environment, developing novel methods for human-robot interaction, and collaborating with hardware engineers to implement and test control algorithms for medical devices. Experience with C/C++, robotics dynamics/kinematics, and control systems is required. | — | 0 |
| Technician, Manufacturing Innovation Technician role focused on operating and maintaining additive manufacturing (3D printing) equipment within a regulated healthcare manufacturing environment. Responsibilities include fleet operation, maintenance, process industrialization, and continuous improvement. | — | 0 |
| MSAT Bio DS Scientific Director/ Fellow Johnson & Johnson is seeking a Fellow / Scientific Director for their Manufacturing Science & Technology (MSAT) Biotherapeutics Drug Substance organization. This role provides scientific and technical leadership for the compliance, resilience, competitiveness, and lifecycle robustness of commercialized and late-stage biologics portfolios. Responsibilities include defining scientific strategy, shaping control strategies, leading technical activities for value optimization and lifecycle management, and resolving complex scientific issues. The role also emphasizes collaboration across global teams, innovation, digital enablement, and advanced analytics. | — | 0 |