Jobs at Johnson & Johnson

Supports clinical sales programs for hospital and physician customers under close supervision. Advises physicians on product clinical attributes and techniques, manages customer account cases, analyzes market and competitive trends, and contributes to growth, customer retention, and competitive positioning initiatives. The role is salaried and eligible for sales commissions.

Develops electrical and embedded systems for surgical robotics and medical devices. Responsibilities include designing and releasing PCB assemblies, developing firmware, integrating sensors and electronics subsystems, creating electrical architectures and requirements, executing verification and validation tests, troubleshooting with laboratory equipment, and collaborating with hardware, software, quality, manufacturing, vendors, and leadership teams.

Manages Japan business operations and sales support for DePuy Synthes, including shipment, sales, pricing, inventory, loaner and sample processes. Leads system implementation, process redesign, master data and pricing cleanup, sell-out process improvements, compliance monitoring, and operational efficiency initiatives. Partners with internal and external stakeholders, manages projects and change management, and leads the operations team.

Leads strategic regional hospital accounts for Shockwave Medical, driving growth through relationship management, complex contracting, reimbursement strategy, pricing discipline, and program implementation. Develops account plans, negotiates system-wide agreements, coordinates cross-functional teams, supports market expansion, conducts business reviews, and ensures contract execution across sales teams. Requires extensive medical device sales leadership experience and travel of up to 50% across the United States.

Manages Saudi immigration, work permits, Iqamas, sponsorship transfers, visas, government platforms, document attestation, and regulatory compliance. Provides HR operational support across onboarding, employee lifecycle processes, employee relations, terminations, Saudization, reporting, and audit readiness. Partners with employees, managers, government authorities, and external agencies while ensuring compliance with Saudi labor and immigration regulations.

A three-year rotational leadership development program for recent graduates across global supply chain functions. Participants gain experience in operations, procurement, quality, planning, logistics, engineering, and manufacturing while leading projects, improving efficiency and compliance, collaborating with suppliers, and developing technical and leadership skills. The program is based in Ciudad Juarez, Mexico, begins in January 2027, and may lead to a permanent position.

Lead development, design, and execution of mass spectrometry assays for characterization and process development of protein therapeutics and conjugates. Evaluate emerging analytical technologies, provide scientific expertise on cross-functional teams, and author compliant protocols, technical reports, and regulatory documents under GMP requirements.

Leads design quality engineering for medical device new product development, from concept through launch and steady-state. Develops product requirements, verification and validation strategies, inspection and sampling plans, test methods, reliability strategies, and risk-management approaches. Ensures compliance with GMP, ISO, FDA design controls, and internal procedures while supporting statistical analysis, defect prevention, continuous improvement, and document approvals. Requires collaboration across engineering, manufacturing, quality, and validation teams, with up to 25% domestic and international travel.

Manages contracts, pricing data, rebate payments, payment validation, reporting, and SOX analysis for pharmacy benefit managers, managed care organizations, and specialty healthcare customers. Partners with internal teams and external organizations, communicates payment status and deadlines, troubleshoots contracting issues, supports process-improvement projects, and develops standard operating procedures. The role also provides analytical insights, training, and cross-functional contract management support.

Leads commercial finance strategy for US/Canada Electrophysiology and Global Neurovascular businesses exceeding $3.5B in annual sales. Oversees forecasting, budgeting, reporting, scenario analysis, demand planning, pricing, incentive strategy, launches, and financial controls. Partners with commercial, R&D, supply chain, and global finance leaders to guide investments and performance. Leads, develops, and coaches a finance team of more than 15 directors, managers, and analysts while supporting enterprise transformation initiatives.

Supports multi-country payroll operations by validating payroll data, performing reconciliations, variance analysis, reporting, remittances, controls, and compliance activities. Coordinates with third-party payroll providers, resolves payroll inquiries, maintains documentation, supports testing and implementation projects, and identifies process improvement and automation opportunities. The role requires confidentiality, accurate execution, collaboration across markets, and knowledge of payroll systems, SOX controls, and statutory requirements.

Lead enterprise Windows endpoint engineering across physical and virtual PCs. Manage Intune-based configuration, compliance, provisioning, patching, application deployment, telemetry, and lifecycle governance. Develop PowerShell automation, troubleshoot complex endpoint issues, improve digital employee experience, establish engineering standards, and collaborate with security and infrastructure teams. Mentor technical engineers and drive reliable, compliant endpoint services in a complex enterprise environment.

Supports pharmaceutical R&D through clinical pharmacology and pharmacometrics activities, including literature review, PK/PD data analysis, trial design, model building, simulation, population modeling, quantitative systems pharmacology, model-based meta-analysis, data visualization, and machine learning. Interns collaborate with multidisciplinary teams across preclinical and clinical development programs in multiple therapeutic areas.

Develops and oversees quality and compliance programs for medical device field inventory, loaner sites, sales offices, and distribution centers. Leads audits, inspections, investigations, remediation, validation, calibration, preventive maintenance, SOP development, process improvements, and regulatory compliance activities. Partners with Quality, Distribution, Sales, Commercial, and Supply Chain teams to resolve issues and improve delivery processes. Supports FDA and ISO 13485 compliance across commercial and distribution operations.

Leads pharmaceutical quality risk management, data integrity, and quality systems activities. Manages site risk registers, conducts complex risk assessments, supports regulatory compliance, and identifies systemic quality issues. Partners with analytics teams to develop dashboards, reports, and data-driven insights. Improves quality review processes, supports digitalization and automation, facilitates change-management risk assessments, and communicates governance information across local and global forums.

Manage approximately €160 million in regional IT procurement spend. Develop and execute category strategies, sourcing plans, negotiations, contracts, supplier performance programs, and value-improvement initiatives. Partner with IT, Procurement, Global Services, business units, legal, and suppliers to meet financial, service, quality, reliability, innovation, compliance, and growth targets. Lead strategic planning, stakeholder relationships, process improvements, supplier collaboration, and implementation of procurement policies and guidelines.

Leads quality operations for a medical device manufacturing site in Costa Rica, including quality systems, compliance, audits, CAPA, complaints, document control, QC testing, calibration, inspections, product release, risk management, validation, and continuous improvement. Manages quality engineering and QC teams, supports manufacturing transfers, interfaces with regulatory and engineering functions, and ensures compliance with medical device regulations. Requires extensive engineering and management experience, bilingual English and Spanish communication, and international travel between Costa Rica and the United States.

Supports immigration and global mobility operations across the Americas, including work permits, visa validation, employee records, documentation, signatures, HRIS updates, vendor coordination, and employee inquiries. The role partners with internal teams and external authorities, advises on mobility administration, supports process improvement and educational town halls, and ensures accurate, customer-focused service delivery within established SLAs.

Manages end-to-end stability oversight and product quality activities across the medicine lifecycle. Develops stability protocols and reports, manages temperature excursions and change controls, supports regulatory filings and escalations, and serves as a stability subject-matter expert. The role works independently on complex, high-value product families, collaborates cross-functionally, identifies improvements, and mentors less experienced team members.

A 10–12-week HR leadership development internship for experienced graduate students. Interns may support strategic consulting and design initiatives across Learning & Development, Change Management, Talent Acquisition, Total Rewards, Organizational Development, HR business partnering, and corporate services. Successful interns may be considered for the full-time HR Leadership Development Program.