Field Service Engineer responsible for installation, service, and repair of medical devices, managing customer technical inquiries and complaints, and performing preventative maintenance. This role involves direct customer interaction, troubleshooting, and administrative tasks related to equipment and service records.

Manufacturing Engineer II role focused on process improvement, root cause analysis, and yield optimization within a regulated healthcare manufacturing environment. Requires a Bachelor's degree in engineering and 2-5 years of experience in manufacturing engineering, with strong problem-solving and data-driven decision-making skills. Experience with nonconformance management, CAPA, and process validation is essential.

Senior Manager for Surgery SC Procurement New Product Development at Johnson & Johnson MedTech. Responsible for leading supplier evaluation, selection, and qualification for key new product launches in specific portfolios. This role involves strategic sourcing, supplier management, contract implementation, and team leadership, requiring strong procurement, business acumen, and cross-functional collaboration.

Senior Design Quality Engineer at Johnson & Johnson MedTech, focusing on new product development and lifecycle management within the Neurovascular team. Responsibilities include ensuring compliance with medical device regulations, leading design control and risk management activities, guiding product development teams, and supporting quality deliverables for R&D projects.

Senior Director role focused on strategic capacity planning and supply chain transfer management within Johnson & Johnson's Innovative Medicine division. Responsibilities include providing end-to-end capacity visibility, optimizing the manufacturing network, developing planning processes for product transfers, driving digitalization, and exploring advanced modeling capabilities. Requires extensive experience in supply chain, planning, and manufacturing within the pharmaceutical industry, with strong analytical, influencing, and leadership skills.

The Director, Transcend will play a critical leadership role within the IM Transcend initiative, a multi-year global business transformation program focused on modernizing end-to-end Supply Chain digital capabilities. This role will support the execution of complex global programs by driving operational excellence, program governance, and cross-functional alignment across key business areas. As a key representative of Supply Chain Quality organization, the Director will ensure that quality perspectives, requirements, and compliance standards are fully integrated into the Transcend program’s strategy and execution. This includes partnering with stakeholders across Supply Chain, Commercial, Finance, Technology, and Quality to embed quality systems and risk-based decision-making into all phases of the transformation. The Director will be responsible for implementing and scaling the program operating model, supporting deployment execution, and leading central workstreams that enable transformation across processes, technology, and data. This role requires strong collaboration with program leads and stakeholders to ensure consistent delivery, risk management, and resource optimization, while also advocating for the unique needs and priorities of Supply Chain Quality function, including Advanced Therapy Quality, Biotherapeutics Quality, Synthetics Quality, and External Quality.

Director Business Process Quality role at Johnson & Johnson, focused on leading a global business transformation program (IM Transcend) for modernizing Supply Chain digital capabilities. The role emphasizes operational excellence, program governance, and cross-functional alignment, ensuring quality perspectives and compliance standards are integrated into the program's strategy and execution. Responsibilities include implementing the program operating model, supporting deployment, leading workstreams, managing interdependencies, and stakeholder engagement, with a focus on Supply Chain Quality functions and GxP/validation requirements.

Internship program at Johnson & Johnson in Bogotá, Colombia, offering opportunities across various departments including Sales & Marketing, Finance, Technology & Innovation, Legal, Medical Affairs, Supply Chain, Manufacturing, HR, Biomedical Engineering, and Project Management. The program aims to provide professional development and a multicultural experience for university students.

Experienced Scientist in Product Development at Johnson & Johnson, focusing on designing, leading, and executing formulation and process development activities for solid and liquid drug product platforms. The role involves evaluating and implementing innovative technologies, supporting cross-functional collaborations, and leveraging digital tools for data analysis and predictive modeling in the development of pharmaceutical therapeutics.

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.

Project Manager role at Johnson & Johnson's Shockwave Medical in Costa Rica, focusing on managing operational projects, ensuring timely and budget-compliant delivery, and overseeing product transfers within the medical device industry. Requires experience with QSR, ISO 13485, and MDR, along with strong project management and cross-functional leadership skills.

Field Reimbursement Manager for Johnson & Johnson's Innovative Medicine division, focusing on Immunology Rheumatology therapies. This role educates healthcare providers (HCPs) and their staff on product coverage, reimbursement processes, prior authorizations, appeals, claims submissions, and coding requirements to ensure patient access to J&J therapies. The position involves significant on-site engagement with HCPs, collaboration with internal teams, and managing territory logistics. Requires a Bachelor's degree and at least 5 years of relevant professional experience in account management and/or reimbursement within the hospital and/or provider setting.

Process Technician role at Johnson & Johnson in Limerick, Ireland, focused on maintaining and optimizing high-volume automated medical device manufacturing lines. Responsibilities include troubleshooting mechanical, electrical, and pneumatic issues, performing maintenance, and collaborating with engineering to resolve complex equipment problems. Requires a minimum Level 6 qualification in a technical discipline and hands-on experience with automated manufacturing equipment.

Senior Director, External Manufacturing – Biotherapeutics role in Titusville NJ, or Horsham PA. Alternative location: Zug, Switzerland. This role is a key leadership position within External Manufacturing, responsible for strategy, execution, and partnership oversight across the full product lifecycle, focused on drug product. The Senior Director will lead global external manufacturing strategy and execution for biotherapeutic drug products, ensuring robust supply, uncompromised quality, operational excellence, and strong CMO partnerships. The role requires close collaboration with R&D, MSAT, Quality, Supply Chain, Procurement, and Regulatory Affairs to ensure seamless product delivery from late-stage development into commercialization. This position is ideal for a leader who combines deep technical and manufacturing expertise with strong enterprise leadership and influence.

Senior Director, External Manufacturing - Biotherapeutics role at Johnson & Johnson, responsible for strategy, execution, and partnership oversight across the full product lifecycle for drug products. Focuses on ensuring robust supply, uncompromised quality, operational excellence, and strong CMO partnerships, collaborating with various internal departments and external partners.

Johnson & Johnson is seeking a Global Head of Advanced Therapies MSAT Lifecycle Management to provide technical and strategic leadership for product lifecycle management within their advanced therapies manufacturing organization. This role involves owning product technology roadmaps, leading cross-functional teams to develop and implement technical solutions, overseeing the implementation of new technologies and automation projects, and driving continuous improvement to enhance manufacturing processes for cell and gene therapy products. The position requires extensive experience in biopharmaceutical manufacturing operations and leadership.

Medical Director role in Gastroenterology Therapeutic Area, US Medical Affairs at Johnson & Johnson. Focuses on developing and executing clinical study programs, evidence generation plans, and contributing to regulatory submissions for GI pipeline and approved products. Collaborates with cross-functional teams to shape clinical and economic value narratives and ensure alignment with business objectives and regulatory standards.

Manager, Standards Management Expert (DAS/TFL) at Johnson & Johnson in Mumbai, India. This role focuses on establishing and maintaining clinical data standards across trials, ensuring compliance with regulatory requirements and industry standards like CDISC, SDTM, and ADaM. Responsibilities include developing specifications for data collection, delivery, analysis, and reporting, and staying updated on industry trends and regulatory changes. The role requires expertise in clinical data tools and collaboration with internal and external partners.

Manager, Standards Management Expert (DAS/TFL) at Johnson & Johnson, focusing on establishing and maintaining clinical data standards across clinical trials. This role requires expert knowledge of regulatory requirements (GCP, ICH) and industry standards (CDISC, SDTM, ADaM, HL7/FHIR, OHDSI/OMOP). Responsibilities include developing specifications for data collection, delivery, analysis, and reporting, ensuring consistency and compliance. The role involves collaboration with internal and external partners, coaching junior colleagues, and staying updated on industry trends and regulatory changes. Experience with clinical data tools like LSAF, Pinnacle 21, or SAS is expected.

Manager, Standards Management Expert (DAS/TFL) at Johnson & Johnson, focusing on establishing and maintaining clinical data standards across trials. This role involves ensuring consistency, compliance with regulatory requirements (GCP, ICH), and expertise in industry standards like CDISC (SDTM, ADaM). Responsibilities include developing specifications for data collection, delivery, analysis, and reporting, and staying updated on industry trends and new technologies.

This is a Quality Engineering Co-Op role at Johnson & Johnson, focusing on identifying compliance gaps in risk documentation for commercialized products, developing a quality mindset through exposure to design controls and risk management, and partnering with cross-functional teams. The role requires enrollment in an engineering degree program and strong communication skills.

Johnson & Johnson is seeking a Health Economics, Market Access & Reimbursement (HEMAR) Senior Associate to support the delivery of market and patient access and funding for J&J's key brands. The role involves supporting health economic plans, developing models, implementing studies, contributing to HTA strategy, and developing submissions to regulatory bodies like NICE, SMC, and AWMSG. The ideal candidate will have a postgraduate degree in Health Economics or a related field, 2-3 years of experience in Health Economics and Market Access, and knowledge of UK healthcare policy and evidence generation.

Sr. Program Manager, Software for Johnson & Johnson's MedTech Surgery team, focusing on the Robotics and Digital Solutions (RAD) franchise. This role will drive the design and development of the Ottava system, managing end-to-end software schedules, OKRs, and risk mitigation using Agile methodologies. The position also involves people management and fostering a collaborative team environment.

This role is for a Clinical Research Manager at Johnson & Johnson's MedTech Electrophysiology team. The manager will lead a team of Clinical Research Leaders and Specialists, ensuring the successful execution and delivery of company-sponsored clinical trials. Responsibilities include overseeing monitoring activities, ensuring compliance with timelines and study milestones, managing budgets, and collaborating with internal and external partners. The role requires adherence to ICH-GCP and company SOPs.

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.

Manager, Cross Therapeutic Area Clinical Risk Management at Johnson & Johnson, responsible for coordinating the identification, assessment, and mitigation of quality risks in clinical trials to ensure data integrity, patient safety, and regulatory compliance. The role involves leading risk monitoring, developing quality plans, providing guidance on quality issues, and supporting inspection readiness activities.

Manager, Clinical Risk Management at Johnson & Johnson, focusing on coordinating the identification, assessment, and mitigation of quality risks in clinical trials to ensure data integrity, patient safety, and regulatory compliance. The role involves data-driven oversight, risk monitoring, and supporting inspection readiness activities within the pharmaceutical industry.

Manager role in Clinical Risk Management for a pharmaceutical company, focusing on ensuring quality, compliance, and patient safety in clinical trials through risk identification, assessment, mitigation, and monitoring. The role involves collaboration with trial teams, R&D colleagues, and regulatory compliance teams to maintain inspection readiness and address quality issues.

Senior Manager for Life-Cycle-Management, Value Stream in the Surgical Vision product portfolio within Johnson & Johnson's MedTech division. This role focuses on owning the lifecycle and operational management, driving the Life-Cycle Management roadmap, and implementing process improvements including AI/Analytics. Requires experience in supply chain operations within a regulated industry and leading technical transfers, launches, and portfolio optimization.

Johnson & Johnson is seeking a Supply Network Planner in Limerick, Ireland, to manage supply network planning for Surgical Vision products, ensuring timely product availability. Responsibilities include propagating net requirements, developing deployment plans, analyzing constraints, managing inventory transfers, and communicating business impacts.

Quality Engineer role at Johnson & Johnson's new lentiviral vector production facility. Focuses on GMP compliance, deviation investigations, change controls, quality risk assessments, and audit support within a pharmaceutical manufacturing environment.

Manufacturing Executive role at Johnson & Johnson focused on leading manufacturing personnel to achieve production goals (Safety, Quality, Volume, Cost). Responsibilities include providing direction, ensuring production flow, managing personnel, driving quality and compliance, and overseeing production scheduling, management, cost, and basic equipment maintenance. Requires an Engineering or Pharma degree with 4-8 years of relevant experience.

Internship role supporting a Supply Chain Analytics project focused on inventory management and optimization within the Orthopaedics Supply Chain organization. Responsibilities include analyzing inventory data, developing concepts for optimized infield inventory levels, and preparing data-driven insights and dashboards.

This role focuses on the research and development of oral drug delivery systems for peptides within the pharmaceutical industry. The scientist will design and develop novel formulations, scout external innovations, and collaborate with cross-functional teams to transform peptides into effective oral solid dosage forms. Responsibilities include contributing to formulation development, strengthening stakeholder relationships, driving innovation with new technologies, executing formulation activities, and ensuring regulatory compliance.

Regional Manager for Johnson & Johnson's Strategy & Corporate Development team, focusing on expanding strategic accounts and building long-term partnerships within the healthcare sector. The role involves developing business strategies, identifying market opportunities, and collaborating with various internal and external stakeholders to drive growth and ensure compliance.

The Material and Contract Manager at Johnson & Johnson is responsible for implementing and overseeing the organization’s materials management and vendor agreements. This role involves executing supply-chain and contract lifecycle tasks, leading cost reduction and supplier risk mitigation efforts, facilitating cross-functional material initiatives, and optimizing processes. The position requires strong analytical and interpersonal skills, with experience in strategic sourcing, contract management, and supplier performance monitoring. The role also involves coaching junior colleagues and integrating company values into decision-making.

R&D Engineer role focused on the design and development of intraocular lenses (IOLs) within a regulated medical device environment. Responsibilities include analyzing requirements, developing product designs and processes, executing validation studies, and ensuring compliance with cGMP and ISO standards. Requires a Bachelor's degree in Engineering with 2-4 years of experience in product/process development in a regulated industry.

This role focuses on market access and reimbursement within the healthcare industry, specifically in Beijing, China. The Assistant Manager will research and analyze national and local medical insurance policies, track policy dynamics, and assess their impact on the medical device industry. Responsibilities include developing company strategies based on policy analysis, identifying market opportunities, managing policy risks, conducting internal policy training, supporting government affairs, and collaborating with internal teams and external stakeholders like industry associations and experts. The role requires a Master's degree or above in public health, medical insurance management, or pharmaceutical policy, with experience in government affairs, policy research, or market access in the medical device or pharmaceutical sector. Strong policy analysis, report writing, strategic planning, communication, and collaboration skills are essential, along with good English proficiency. Project management or internal training experience is a plus.

This role is a Regional Technology Specialist for Johnson & Johnson MedTech's Electrophysiology division. The primary focus is on sales support, clinical competency development, and training for field sales and service personnel, as well as providing technical and clinical product support to physicians and lab staff. The role involves assessing and improving clinical skills, launching new technologies, and building relationships with healthcare professionals to drive product utilization and business objectives. It is a sales-adjacent role focused on product education and support within the medical device industry.

This role is for a Sr. Manager, Product Management focused on Patient Experience within Johnson & Johnson's IT department. The primary responsibility is to lead the strategy, development, and management of CRM and digital capabilities for Patient Support Programs. This includes owning the product lifecycle, defining roadmaps, collaborating with stakeholders, ensuring compliance with regulations like HIPAA, and driving continuous improvement of patient-centered digital solutions. The role emphasizes product leadership, stakeholder collaboration, and delivery in a regulated healthcare environment.

Senior Financial Analyst role at Johnson & Johnson supporting Ethicon manufacturing operations in Puerto Rico. Responsibilities include financial control, business planning, forecasting, cost accounting, financial reporting, and analysis for manufacturing operations. Requires a bachelor's degree in Accounting/Finance, 3+ years of finance experience, and bilingual Spanish/English skills.

The Associate Site Manager will serve as the primary contact point between the Sponsor and the Investigational Site, ensuring inspection readiness through compliance with clinical trial protocol, SOPs, GCP, and applicable regulations and guidelines. This role involves site selection, recruitment planning, monitoring, and close-out activities, ensuring data accuracy, timely query resolution, and proper documentation.

The Strategic Capabilities Analyst role at Johnson & Johnson focuses on developing and implementing technical solutions and data-driven performance management capabilities within the Electrophysiology Supply Chain. Responsibilities include creating Python scripts for data analysis, designing PowerBI dashboards, managing SQL databases, developing automated reporting, building data pipelines, and performing root cause analysis. The role requires proficiency in Python, SQL, PowerBI, and an understanding of cloud computing, with basic machine learning and statistical analysis capabilities.

Manager role focused on developing and improving business processes and capabilities within the Supply Chain Planning function for Johnson & Johnson Medical Devices. The role involves strategic planning, cross-functional partnership, and overseeing the execution of technical capabilities to support business strategy.

This role is for an Associate Clinical Account Specialist in MedTech Sales, focusing on Electrophysiology. It involves a training program to become a Clinical Account Specialist, providing expert clinical product and technical assistance to physicians and staff during procedures. The goal is to meet business objectives within an assigned territory. The role requires a Bachelor's degree or equivalent experience, a valid driver's license, and willingness to travel.

This postdoctoral scholar position is an opportunity within the protein formulations group in Drug Product Development & Delivery (DPD&D). This position will be a lab-based role. The postdoctoral scholar will be responsible for experimental studies to evaluate and characterize the efficacy of molecular chaperones as therapeutic protein stabilizers. Therapeutic proteins to be evaluated include mAbs, bispecifics and multispecifics. This includes development and optimization of the technical operations associated with biologics development, high protein concentration feasibility, molecular chaperone screening, biophysical analysis of protein therapeutics, analysis of small molecule / mAb interactions, protein formulation optimization, and stability campaigns. Where applicable, the postdoctoral scholar will be exposed to, and potentially assist with, computational evaluation of small molecule / mAb interactions. The postdoctoral scholar will work independently as well as with cross-functional teams to support project needs and meet project deliverables.

This role is for an Associate Clinical Account Specialist in Electrophysiology (EP) within Johnson & Johnson MedTech. It's a training position for individuals with little to no EP experience, leading to a Clinical Account Specialist role. The primary focus is providing clinical product and technical assistance to physicians and staff on medical systems and equipment during procedures, with the goal of meeting business objectives. The role involves extensive training, understanding EP lab dynamics, and maintaining strong communication with internal and external partners.