Jobs at Johnson & Johnson

Leads procurement strategy and supplier management for CSS materials and electronic systems, overseeing approximately $100 million in spend. Responsibilities include category planning, supplier sourcing, contract and price negotiations, cost reduction, new product development sourcing, market analysis, compliance, risk management, and procurement team leadership. Collaborates with R&D, engineering, quality, finance, and other stakeholders to support MedTech growth.

Leads the Global Vision Deliver product and Surgical Vision ERP platform, defining strategy, roadmaps, priorities, and measurable outcomes. Oversees SAP ERP delivery from discovery through deployment, lifecycle management, reliability, compliance, cybersecurity, and operational transition. Manages budgets, capacity, suppliers, governance, risks, and platform modernization. Leads global cross-functional teams, coaches product owners, and partners with business, engineering, quality, security, and technology stakeholders to deliver scalable and compliant solutions.

Lead procurement strategy for Electrophysiology and Neurovascular components and commodities, overseeing approximately $200 million in spend. Manage supplier relationships, negotiations, contracts, cost optimization, innovation sourcing, market analysis, compliance, risk, and new product development support. Collaborate with R&D, engineering, quality, finance, and other stakeholders while leading and developing a procurement team in a regulated MedTech manufacturing environment.

Leads quality engineering activities for medical device new product development and lifecycle management. Oversees design controls, risk management, validation, NCRs, quality systems, statistical analysis, failure investigations, and regulatory compliance. Develops test methods and protocols, supports sterility and packaging requirements, coordinates engineering projects, and mentors quality engineers. Collaborates with R&D, Operations, and cross-functional leadership to ensure compliant product development, transfer, and continuous improvement.

Leads quality engineering activities for medical device new product development and lifecycle management. Develops risk management plans, FMEAs, validation protocols, design controls, test methods, and quality processes. Performs statistical analysis using SPC, DOE, ANOVA, and Gauge R&R; supports NCR resolution, failure analysis, root-cause investigations, equipment qualification, and manufacturing transfer. Collaborates with R&D and operations, oversees compliance with quality systems and applicable regulations, manages complex engineering projects, and provides technical leadership and coaching.

Leads and develops District Managers and Sales Specialists across the West Region for the RYBREVANT oncology franchise. The role drives compliant sales growth across lung and head and neck cancers, develops regional business plans, oversees account goals and performance metrics, coaches teams, and collaborates with sales, marketing, access, pricing, and commercial partners. Candidates need substantial pharmaceutical or healthcare commercial experience, people leadership, oncology expertise, and willingness to travel up to 50%.

Leads downstream marketing and commercialization for Shockwave Medical’s IVL product portfolio. Oversees product positioning, launches, pricing, market segmentation, brand strategy, communications, medical conferences, evidence strategy, and portfolio planning. Partners with sales, clinical, R&D, regulatory, manufacturing, finance, physicians, and senior leadership while monitoring market trends and reimbursement. Builds and develops high-performing marketing teams and supports global commercialization in a regulated medical device environment.

Leads Mentor's global digital marketing strategy, transformation, campaigns, websites, social media, content operations, customer experience, marketing technology, analytics, and governance. Manages a five-person team, global agencies, technology partners, budgets, and cross-functional stakeholders. The role drives compliant omnichannel marketing, brand growth, digital capability development, AI adoption, website optimization, content localization, performance measurement, and enterprise-wide change across a highly regulated MedTech environment.

Leads global MedTech Communications & Public Affairs strategy, operations, transformation, governance, analytics, technology enablement, budget and vendor management, and capability building. Partners with senior leaders to improve operating models, measure communications impact, advance AI and digital adoption, lead change, strengthen culture, and align the function with enterprise priorities. Oversees teams, cross-functional initiatives, executive reporting, scalable processes, and global stakeholder partnerships.

Leads and supports neurovascular medical device clinical trials from feasibility through closure. Responsibilities include site and vendor management, trial documentation, monitoring, clinical data review, investigator agreements, budgets, regulatory and ethics interactions, evidence generation, post-market follow-up, and safety reporting. The role also mentors study resources, supports new product development and lifecycle management, and ensures compliance with applicable regulations, SOPs, and clinical research standards.

Lead and manage company‑sponsored neurovascular clinical trials end‑to‑end: feasibility, site selection, setup, conduct, monitoring, data review and closure. Develop trial documents, manage investigational devices and vendors, ensure regulatory and safety reporting compliance, support evidence generation and cross‑functional alignment, mentor study staff, and deliver projects on time and within budget.

Develops scientific manuscripts, abstracts, posters, presentations, and evidence-dissemination materials for cardiovascular and electrophysiology clinical studies. Analyzes and communicates clinical data, coordinates document reviews and approvals, collaborates with clinical, statistical, medical affairs, marketing, and physician stakeholders, and supports congress activities. Ensures compliance with publication, regulatory, ethical, and clinical practice standards while monitoring therapeutic-area literature and trends.

Leads financial planning and analysis for MedTech R&D, including budgeting, forecasting, project spend, headcount, capital planning, reporting, and quarterly close. Advises R&D leaders on financial decisions, tracks performance against plans, identifies risks and opportunities, ensures SOX compliance, improves processes and reporting automation, and supervises and develops team members.

Leads global strategic marketing, innovation, portfolio strategy, product launches, brand management, business insights, and growth for MENTOR’s breast implant and reconstruction portfolio. Oversees positioning, pricing, forecasting, customer insights, commercialization, lifecycle management, and collaboration with R&D, clinical, regulatory, medical, supply chain, and regional marketing teams. Develops talent, manages budgets, monitors competition, and drives global business results.

The Senior Financial Analyst supports forecasting, financial close, reporting, budgeting, resource allocation, compliance reviews, and complex financial analysis for Scientific Affairs. The role presents performance results to leadership, advises business partners, identifies investment and expenditure opportunities, improves processes through automation and standardization, and participates in financial transformation initiatives.

Leads global electrophysiology market forecasting, market-model development, competitive intelligence, market-share reporting, scenario analysis, and new-product forecasting. Integrates internal and external data into executive-ready strategic narratives and recommendations. Partners with marketing, finance, supply chain, clinical, regional teams, and senior leadership to support business planning, demand planning, portfolio decisions, and process governance across a global MedTech organization.

Leads J&J MedTech’s global UDI program, ensuring compliance with FDA, EU MDR, and international regulations. Owns UDI processes, controls, data governance, system capabilities, audits, inspections, regulatory trend monitoring, and continuous improvement. Partners with Regulatory Affairs, IT, Supply Chain, Manufacturing, R&D, and Commercial teams globally while coaching stakeholders and supporting scalable quality and compliance processes.

Leads data governance and stewardship programs for regulated MedTech data. Implements access controls, usage policies, data quality and lineage practices, governance automation, audit workflows, metrics, and compliance processes. Partners with business, technical, and compliance teams to govern clinical, preclinical, commercial, and product data. Supports tooling evaluations, issue remediation, process improvement, stakeholder presentations, and coaching of junior colleagues.

Develop and deploy automated computational workflows for structure-based drug discovery, including ligand and protein preparation, docking, free-energy calculations, and co-folding. Collaborate with platform, IT, cheminformatics, and drug discovery teams to advance automated design-make-test-analyze cycles, incorporate new tools, and align workflows with enterprise standards. Apply strong programming, workflow orchestration, software engineering, and emerging AI capabilities to accelerate pharmaceutical research.

Conduct translational ADME research on PROTACs, molecular glues, and RIPTACs. Develop intestinal permeability models, evaluate lymphatic absorption and secretion, perform mechanistic in vivo studies, and apply PBPK and computational modeling. Integrate experimental data to identify determinants of oral bioavailability and tissue permeability, guide therapeutic optimization, communicate findings, and publish results in collaboration with pharmaceutical scientists.