Jobs at Johnson & Johnson

Ensure quality and regulatory compliance for facility management, infrastructure projects, and EHS. Manage documentation, CAPA/RCA, audits, SOPs, and interface with Engineering, Operations and global Quality to drive continuous improvement.

Serve as the technical liaison between product development and suppliers to define DfX, develop manufacturing assembly and test strategies for electrical sub-assemblies, qualify suppliers and test systems, execute TMVs, lead risk assessments and process validation (IQ/OQ/PQ), and support incoming inspection and troubleshooting during NPI.

Lead product ownership for global Order-to-Cash technology (starting with SAP S/4 SD and satellite apps) to design, integrate, and optimize credit, pricing, billing, invoicing, and reporting. Partner with Finance, Commercial, and Supply Chain to ensure SOX-compliant, scalable ERP solutions, drive analytics and automation, manage vendors/system integrators, and coach teams to deliver measurable financial and operational outcomes.

Lead technical squad for Clinical Operations software: design, build, validate, deploy, and maintain secure, compliant, scalable solutions. Mentor engineers, drive CI/CD and test automation, manage integrations, technical debt, and regulatory readiness while partnering with product and clinical stakeholders.

Execute marketing strategies to achieve sales targets; segment and manage target customers, schedule visits, and accurately convey product information; organize compliant academic presentations and support regional events; maintain market and sales data; assist manager with tenders, reimbursement (医保) tasks and other assigned duties.

Lead end-to-end payments and invoice processing for assigned market clusters, ensuring KPI and SLA adherence. Act as primary contact for stakeholders and suppliers, manage escalations, enforce controls and SOPs, support audits, coach and oversee team and BPO resources, monitor performance, drive root-cause analysis and process improvements, and coordinate with Treasury, Procurement, and regional finance leaders.

Promote immunology pharmaceutical products to healthcare professionals across a territory, build and maintain hospital account relationships, generate sales forecasts and reports, identify growth opportunities, perform product listing, and collaborate cross-functionally to resolve customer issues and achieve sales objectives.

Lead a MedTech joint replacement sales team to achieve revenue and market share targets through territory planning, clinical support in theatres, KOL and hospital relationship-building, forecasting, contract/tender management, and cross-functional coordination while ensuring regulatory and ethical compliance.

Lead Health Care Compliance for R&D and External Scientific Innovation in China. Partner with R&D, ESI, and cross-functional leaders to identify, assess, and mitigate compliance and anti-corruption risks. Manage and coach an HCC team, implement compliance programs aligned with J&J guidelines and DOJ hallmarks, drive digital transformation of compliance, and support global/regional initiatives.

Perform end-to-end accounting for balance sheet and income statement processes, ensure timely period close and SOX compliance, maintain reconciliations, support audits, train new team members, drive process improvements and act as trusted business partner across regions.

Support Product Owner and squad to translate clinical operations needs into user stories, requirements, process documentation, and reports. Aid backlog refinement, acceptance testing, metrics tracking, and compliance-aligned SDLC documentation to enable high-quality digital product delivery for clinical operations.

Design and develop robotic surgical hardware by creating and modifying CAD models and drawings, managing large assemblies, producing production drawings, MPIs and BOMs, coordinating with engineering and vendors, writing component specs, and submitting engineering change orders.

Serve as the Payments subject-matter expert for assigned clusters, executing payment processing, verifications, reconciliations, and exception handling. Maintain controls and compliance, support audits, perform root-cause analysis, resolve operational issues, and escalate risks. Coach and train Associates/Specialists, engage stakeholders (Finance, Procurement, Treasury), and contribute to process improvement, standardization, automation, and UAT for transformation programs.

Serves as a microbiological quality and sterility assurance subject matter expert for medical devices. Develops and validates radiation sterilization and reusable-device reprocessing processes, coordinates EO sterilization requalification, investigates nonconformances, evaluates trends and OOS results, supports corrective actions and product disposition, prepares change-control documents, and writes SOPs and validation documentation while ensuring GMP/GDP compliance.

Leads commercial analytics and AI workstreams for MedTech, evaluating campaigns, customer engagement, channel performance, and sales outcomes. Develops data products, semantic models, KPI frameworks, curated datasets, and automated pipelines. Partners with Marketing, Sales, Data Science, Technology, and vendors to build and manage conversational and Agentic AI analytics solutions. Presents insights and recommendations to senior leaders, supports data-driven decisions, monitors AI performance, and maintains trusted commercial data foundations.

Partner with business leaders at the Leeds and Blackpool DePuy Synthes sites to drive talent strategy, change management, employee/labor relations, and organizational development. Coach leaders, design talent pipelines, implement HR strategies, and support engagement and performance to enable business results. Role includes cross-site support and up to 20% travel.

Manufacturing Engineer leading new product introduction for robotic medical device systems. Responsibilities include designing and validating assembly processes, tooling, gauges, and fixtures; maintaining manufacturing and quality documentation; troubleshooting electromechanical systems; conducting root cause analysis; supporting process characterization and validation; and driving continuous improvement with cross-functional R&D, Quality, and Production teams.

Leads parenteral drug product manufacturing projects, including new product introductions, technology transfers, engineering runs, clinical and validation batches, process improvements, change controls, and documentation updates. Acts as a subject matter expert for audits, inspections, regulatory filings, and health authority responses. Collaborates with Operations, Engineering, and MSAT, trains manufacturing teams, and ensures compliance with GMP, EHS, and SOX requirements.

Leads healthcare compliance strategy and operations for Malaysia, Thailand, and potentially other Southeast Asian markets. Manages compliance risks, controls, training, monitoring, investigations, audits, regulatory interactions, and issue remediation. Advises senior business leaders, partners with Legal and cross-functional teams, monitors regulatory developments, and promotes ethical conduct across DePuy Synthes’ Orthopedics business.

Leads the LATAM commercial education strategy for DePuy Synthes, integrating clinical and strategic selling capabilities across direct and distributor-led models. Manages the regional education team, partners with commercial and cross-functional leaders, supports product launches and platform adoption, governs program execution, and measures capability-building effectiveness. The role drives coaching, field reinforcement, continuous learning, and commercial performance improvement across diverse markets and channels.