Jobs at Johnson & Johnson

Leads Japan medical-device complaint handling, adverse-event assessment, post-market surveillance, regulatory reporting, investigations, trending, and inspection readiness. The role coordinates with technical, clinical, quality, regulatory, manufacturing, sales, and global teams; maintains compliant documentation; supports audits and corrective actions; provides technical guidance; and drives continuous improvements across vigilance and quality-system processes.

Execute Account-to-Report and general accounting activities for Global Services Finance: process sales/purchase orders, reconcile balance sheets, close periods per SLA and SOX, support audits, train team members, act as team lead backup, drive continuous improvement and maintain compliance with worldwide policies.

Lead development and integration of automation-enabled biologics optimization workflows, connecting experimental data, computational/AI approaches, and engineering to accelerate antibody/protein discovery. Drive platform development (yeast display, NGS, high-throughput assays), partner with cross-functional teams, evaluate emerging technologies, and translate sequence-structure-function data into optimization strategies, publications, and IP.

Leads commercial operations at an orthopaedic medical device site, serving as backup to the Site Lead and coordinating sales office activities. Responsibilities include inventory processing, operational metrics, sales collaboration, customer service, supply chain coordination, Lean process improvement, and compliance with documentation, regulatory, quality, and safety standards. The role requires managing team responsibilities, improving outbound efficiency, and supporting customer order collection and issue resolution.

Leads complex employee relations investigations across APAC and EMEA, managing intake, interviews, evidence review, findings, documentation, recommendations, and case closure. Ensures consistent, timely, legally compliant outcomes for sensitive matters involving discrimination, harassment, retaliation, and other workplace concerns. Partners with HR and Legal, maintains audit-ready records, identifies systemic trends, prioritizes risk, guides HR stakeholders, and improves investigation processes and tools.

Supports laboratory quality control activities, including sample receipt and management, reagent and supply handling, housekeeping, finished-goods testing, data review, metrics reporting, investigations, qualification and validation activities, and continuous improvement initiatives under supervision. Reviews quality analysis results, reports issues, and assists with risk mitigation while applying Quality Control standards and company principles.

Leads Johnson & Johnson’s global Regulatory Data Office, overseeing regulatory data governance, stewardship, quality, standards, and the Regulatory Data Hub. Chairs the Regulatory Data Council and partners with R&D, IT, data science, and AI teams on regulatory transformation, including RIM, eLabeling, MDM, and submission-excellence initiatives. Manages global data stewards, drives trusted data adoption, ensures compliance with regulatory standards, and connects data governance with process excellence and decision enablement.

Develops and reviews clinical trial programming deliverables including CDISC SDTM submission packages, data model specifications, mappings, edit checks, listings and study-specific reports. Aggregates and transforms clinical data sources, performs quality control and verification, and supports process, system and tool improvements to ensure compliance and fit-for-purpose reporting to monitor safety, risk and regulatory requirements.

Leads the global SAP Finance Account-to-Report product organization, setting strategy and delivering SAP S/4HANA Finance solutions, enhancements, and support. Translates finance business needs into technology roadmaps, oversees solution design, testing, compliance, value realization, and continuous improvement. Partners with finance and technology leaders, manages internal and external resources, and directs vendor relationships and project delivery. Requires deep SAP Finance expertise, financial accounting knowledge, team leadership, and experience managing enterprise transformation initiatives.

Leads quality and technical initiatives in a regulated manufacturing environment. The role manages non-conformance investigations, CAPA and root cause analysis, regulatory compliance, audits, process validation, and continuous improvement using Lean, Six Sigma, FMEA, and statistical analysis. It partners with Manufacturing, Engineering, Quality, and Supply Chain teams, analyzes quality trends, supports operational excellence, and supervises and develops quality and technical professionals.

Leads proactive post-marketing pharmacovigilance signal detection, validation, evaluation, and surveillance for complex pharmaceutical products. Develops surveillance plans, analyzes global safety databases and emerging trends, communicates findings to safety teams, supports regulatory and clinical documents, and evaluates computer-assisted methodologies. The role provides technical leadership, stakeholder training, mentoring, cross-functional influence, and occasional indirect people management while supporting global safety strategy and risk management.

Supervise medical device manufacturing operations, production personnel, and resource utilization while meeting safety, quality, compliance, efficiency, waste, and production targets. Provide technical leadership for process improvements, pilot operations, validations, product introductions, and process transfers. Drive lean manufacturing, employee development, EHS compliance, quality systems adherence, and issue resolution while coordinating with support functions and Human Resources.

Leads North American service sales execution for a robotic surgical platform, including service-plan positioning, warranty conversions, renewals, retention, upselling, pipeline forecasting, and account growth. Builds partnerships with capital sales and customer success teams, manages commercial relationships, supports negotiations, and coordinates cross-functional customer execution. The role will eventually recruit, coach, and lead service sales representatives and renewal specialists while ensuring compliance with quality, regulatory, privacy, legal, and healthcare requirements.

Leads multidisciplinary medical device R&D projects for breast implants, tissue expanders, and related products. Responsibilities include conceptualization, design, prototyping, testing, verification and validation, regulatory clearance, design transfer, intellectual property development, and collaboration with clinical, regulatory, quality, manufacturing, marketing, and external partners. The role also supports product improvements, manages vendors, coordinates technical reviews, and may supervise engineers or technicians.

Leads pharmacovigilance signal detection and validation for complex pharmaceutical products using post-marketing safety data. Develops surveillance plans, evaluates adverse event trends, conducts data mining, communicates findings to safety and product teams, and guides signal evaluation strategies. The role also advances computer-assisted methodologies, mentors scientists, trains stakeholders, supports regulatory and clinical documentation, and provides technical leadership across signal management programs.

Leads technical product ownership for finance, planning, forecasting, data, and analytics solutions. Defines product vision, business value, roadmaps, functional designs, and KPIs while partnering with finance, technology, business process owners, and vendors. Oversees data modeling, governance, reporting, ERP integration, experimentation, agile delivery, compliance, and continuous improvement. Manages competing priorities and develops high-performing teams supporting MedTech transformation.

Leads a global portfolio of privacy and legal technology products, defining strategy, prioritizing investments, guiding delivery, and identifying automation and AI opportunities. Partners with business, engineering, security, and product teams to deliver secure, scalable solutions and improve user experiences. Supports a cross-functional team, drives continuous improvement, and uses data-informed decisions to advance digital transformation across Privacy and Legal organizations.

Leads MedTech Brazil’s accounting close, financial compliance, SOX controls, audit support, financial planning, risk remediation, and process improvement. Partners with business and Finance stakeholders, applies analytics and AI to automate controllership activities, and manages and develops a team of analysts. Ensures compliance with BRGAAP, USGAAP, IFRS, corporate policies, statutory requirements, and responsible AI practices.

Leads Knowledge Management, operational intelligence, service reliability, continuous improvement, and data governance across MedTech R&D applications. Develops dashboards, analyzes service and support data, improves CMDB quality, identifies reliability risks and automation opportunities, and supports AI-ready knowledge foundations. Partners with product, operations, reliability, support, and vendor teams to improve service quality, self-service adoption, issue resolution, operational efficiency, and application portfolio governance.

Owns process systems and equipment packages for GMP biologics manufacturing facilities from design through turnover. Leads vendor coordination, construction support, commissioning, qualification, punch-list closure, issue resolution, change control, and GMP readiness. Partners with engineering, construction, manufacturing, quality, vendors, and other cross-functional teams to deliver systems safely, on schedule, within budget, and in compliance with approved specifications and regulatory requirements.