Jobs at Johnson & Johnson

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.

Leads Source-to-Contract procurement operations across the Americas, including sourcing events, negotiations, contract drafting and execution, stakeholder management, compliance, and SLA delivery. Mentors analysts, drives process improvements, supports automation and AI initiatives, owns S2C tool enhancements, and partners with procurement, legal, compliance, IT, and security teams. The role also supports data governance, privacy, cybersecurity, and regulatory requirements while managing relationships with business partners and category teams.

Coordinates manufacturing employee training, onboarding, qualification activities, curricula, and LMS administration. Maintains audit-ready training records, tracks compliance and competency, provides leadership reporting, supports audits, and partners with supervisors and subject matter experts to improve training effectiveness and regulatory readiness.

Leads end-to-end procurement strategy for Johnson & Johnson’s Spine, Sports Medicine, and CMFT platforms. Oversees strategic sourcing, supplier management, contracting, risk mitigation, business continuity, network transformation, acquisitions, external manufacturing, product transfers, and value creation. Partners with R&D, operations, finance, quality, regulatory, and commercial teams while engaging supplier executives. Leads a geographically dispersed procurement team and drives financial performance, innovation, resilience, and operational execution.

Develops dashboards, visualizations, reports, and metrics to monitor pharmacovigilance quality and compliance. Troubleshoots data issues across source systems, pipelines, warehouses, semantic models, and reporting layers. Provides user training, documentation, metrics support, and continuous improvement recommendations while collaborating with medical safety, business, and technology teams in a validated environment.

Supports the adoption, integration, optimization, testing, validation, deployment, and stabilization of manufacturing applications, primarily MES. Partners with manufacturing, quality, engineering, automation, project, and IT teams to address operational needs, maintain accurate workflows and reporting, support production changes and new product introductions, resolve issues, and improve manufacturing processes in production environments.

Leads the site's environmental, health, and safety programs, ensuring regulatory and corporate compliance. Manages audits, inspections, hazardous waste, emergency response, occupational health services, risk controls, scorecards, and continuous improvement. Acts as the site EHS representative, leads emergency response teams, supports business continuity, manages budgets and projects, and guides teams toward safe working practices. Requires expertise in EHS regulations, medical device or pharmaceutical environments, ISO standards, audits, and people leadership.

Manages quality assurance, compliance, audits, technical support, and quality agreements for external contract laboratories supporting pharmaceutical R&D and supply chain operations. Leads ECL qualification, corrective actions, risk management, deviation closure, cGMP oversight, business reviews, continuous improvement, and regulatory compliance. Collaborates with global quality, laboratory, procurement, and technical stakeholders, with up to 20% global travel for audits and site oversight.

Leads manufacturing process excellence and continuous improvement initiatives across plant operations and supply chain. Develops strategic plans, manages improvement projects, tracks performance measures, trains teams, and communicates results to plant leadership. Applies Six Sigma, Lean manufacturing, DMAIC, and JJPS methods while supporting quality, safety, environmental, regulatory, and cost objectives. May supervise engineering technicians and requires collaboration across departments and sites, with up to 10% travel.

Leads the global strategy and execution of legal template transformation within Johnson & Johnson’s contracting program. Responsibilities include simplifying and governing templates, clauses, playbooks, and fallback positions; establishing operating models and governance; leading localization, deployment, adoption, and continuous improvement; measuring outcomes; and aligning Legal, business, technology, and enabling functions. The role also manages team members and partners while driving enterprise transformation through technology, data, automation, and responsible AI.