Manager, ASPAC Contracting role at Johnson & Johnson, focusing on leading regional IT commercial strategy for LATAM, partnering with Commercial, Marketing, Sales, and Regional leadership to enable growth through scalable, compliant, and data-driven digital solutions. The role involves overseeing the delivery of commercial systems and platforms, driving portfolio planning, and ensuring compliance with security, privacy, quality, and regulatory standards. This is a people leader position within the Technology Product & Platform Management function.

This role is for a Customer Experience and Professional Education Specialist at Johnson & Johnson's Sydney Institute. The primary responsibilities include serving as an onsite experience ambassador, managing the intake and scheduling of Institute events, coordinating with event leads, and ensuring high-quality, compliant learning experiences for customers and healthcare professionals. The role also involves supporting the Professional Education strategy, maintaining site processes, managing vendor partnerships, and ensuring compliance with regulatory requirements.

Associate Director, Regulatory Affairs for the UK & Ireland market, focusing on medical device compliance, market access, and lifecycle management within a regulated environment. This role involves leading regulatory strategy, ensuring compliance with UK and EU regulations (MDR, UKCA), managing regulatory risk, and partnering with cross-functional teams. The position also includes team leadership and engagement with policy initiatives.

Commercial Lead for DePuy Synthes, a Johnson & Johnson orthopaedics company, based in Leeds, UK. This role leads and executes commercial NHS activities, manages relationships with NHS Supply Chain and other stakeholders, shapes agreements, coordinates pricing and tenders, and ensures commercial governance. Requires strong knowledge of NHS procurement, contracting, and the UK healthcare system, with an emphasis on driving results and customer-centric value.

This role is responsible for ensuring the accuracy, consistency, and quality of master data across various commercial systems and applications. It involves managing the end-to-end master data lifecycle, implementing best practices in data governance, protection, and compliance with regulations like GDPR. The role also includes collaborating with stakeholders, developing data management strategies, identifying data process enhancements, utilizing tools like Power BI and Excel for reporting, and participating in the implementation of new Master Data Management (MDM) systems.

Director, Global Trade Operations Lead responsible for setting and leading the global trade operations strategy to ensure compliant, efficient, and resilient cross-border movement of products worldwide. This role provides enterprise leadership across customs, import/export operations, trade compliance execution, and governance, while enabling business growth and supply continuity.

The Export Control Analyst supports global trade compliance activities by ensuring products, technologies, and data are exported in compliance with applicable export control laws and regulations. This role involves screening, classification, transaction reviews, and maintaining records within a regulated medical technology environment.

This role leads Health Economics & Market Access (HEMA) strategy and execution for Johnson & Johnson's DePuy Synthes in the United Kingdom. It involves shaping access strategy, engaging with payers and HTA bodies (like NICE), ensuring reimbursement, and demonstrating the value of innovative orthopaedic solutions. The role also requires cross-functional collaboration and compliance with regulatory requirements.

This role manages day-to-day import and export operations, ensuring compliance with international trade regulations and company policies. It involves preparing and reviewing trade documentation, coordinating with freight forwarders and customs brokers, and ensuring adherence to customs laws. The role also focuses on maintaining accurate records, identifying process improvements, and supporting cross-border material flows within a regulated medical device environment.

Johnson & Johnson is seeking an Operations, Strategy & Execution Lead to support the GM/LT with the execution of strategic priorities, manage governance structures, track execution against priorities, and lead cross-functional program management. The role involves translating regional/global strategy into measurable plans, facilitating financial planning cycles, and improving decision quality and execution.

This role is for a Private Sector Lead at Johnson & Johnson's DePuy Synthes (orthopaedics business). The lead will drive business growth by accelerating strategies through private sector groups and independent hospitals, identifying new partnership opportunities, and developing senior C-suite relationships. Responsibilities include leading the private sector growth plan, managing relationships, optimizing value-based procurement, and shaping innovative proposals. The role requires strong project management, commercial capability, knowledge of UK healthcare procurement, negotiation skills, and the ability to influence senior stakeholders.

This role is for a Service & Solutions Manager at Johnson & Johnson's DePuy Synthes business in Leeds, UK. The manager will deploy the company's value offering to drive market share with strategic customers, focusing on Clinical Transformation, Theatre Efficiency, Patient Pathway programs, and enabling technology. The role involves program management, relationship management with NHS trusts and private sector organizations, and partnering with commercial teams to deliver the value strategy. It requires strong project management, understanding of value-based strategies, excellent communication, and knowledge of the UK Healthcare system and medical devices industry.

This role is a Commercial Capability Lead for Johnson & Johnson's DePuy Synthes within the UK & Ireland. The primary focus is on managing and improving pricing, contracting, and tendering strategies to meet sales objectives. It involves managing teams, contributing to business growth through process improvement and automation, and developing strategic sales plans based on customer insights and data. The role also includes performance metric generation and stakeholder relationship management.

This role is responsible for executing and supporting regulatory compliance activities related to sourcing, suppliers, and externally provided processes within a regulated healthcare industry. It ensures suppliers comply with regulatory requirements, quality system standards, and internal policies, impacting product quality and audit readiness.

This role is for a Value Lead at Johnson & Johnson's DePuy Synthes in Leeds, UK. The primary focus is to lead, shape, and deliver the company's value proposition through a team of S&S managers, aligning with healthcare and customer needs. Responsibilities include managing value-based procurement conversations, developing long-term partnership agreements, and driving business growth through innovative proposals and collaboration across internal and external stakeholders, particularly within the NHS/Private customer base.

Admin Assistant role at Johnson & Johnson supporting teams in a MedTech environment. Responsibilities include scheduling, travel arrangements, expense tracking, preparing correspondence, maintaining records, and basic project coordination. Requires 6-8 years of administrative experience and proficiency in office software.

Executive Assistant role supporting senior commercial leaders in the healthcare industry. Responsibilities include calendar management, meeting coordination, travel arrangements, preparing presentations and reports, coordinating internal meetings, serving as a point of contact, supporting commercial initiatives, managing expenses, and maintaining records. Requires strong organizational skills, attention to detail, discretion, and proficiency in Microsoft Office. Fluency in English is required.

Johnson & Johnson is seeking a Field Service Engineer for their VELYS™ robotic-assisted orthopedic technologies in Aprilia, Italy. The role involves installation, maintenance, troubleshooting, and optimization of these systems in clinical and customer environments, ensuring safe, reliable, and compliant operation. The engineer will provide on-site support during surgical cases, perform preventive maintenance, and collaborate with various teams to ensure system uptime and customer satisfaction.

This role focuses on contract administration and management within the healthcare sector, specifically for Johnson & Johnson's market access function. It involves reviewing data, administering processes, implementing pre-sale and post-signature support, and communicating with stakeholders to ensure contract compliance. The role also involves research and analytics for offer development and coaching junior colleagues.

Manager, LOC EMEA Regulatory Compliance role at Johnson & Johnson (DePuy Synthes) in Zug, Switzerland. Responsible for leading and coordinating regulatory compliance activities across EMEA Local Operating Companies, ensuring adherence to regulatory requirements, quality system standards, and internal policies. Involves leading internal audits, supporting external audits and inspections, interpreting regulatory requirements, monitoring compliance risks, and driving continuous improvement. Requires a Bachelor's degree and 6-8 years of experience in Regulatory Compliance or Quality within a regulated industry, with strong knowledge of EMEA regulatory requirements.

Johnson & Johnson is seeking a HEMA Lead for Switzerland and Austria to lead Health Economics & Market Access strategy and execution for innovative orthopaedic solutions. This role involves developing country-specific access plans, building relationships with payers and authorities, generating evidence, and partnering cross-functionally to ensure reimbursement and adoption.

Manager, RA Italy is responsible for leading regulatory affairs activities for the Italy local market, ensuring compliance with Italian and EU regulatory requirements for DePuy Synthes products, and enabling timely market access and lifecycle management. This role partners with Commercial, Quality, Supply Chain, and Global Regulatory teams within a highly regulated environment.

This role is for a Senior Regulatory Compliance Specialist in EMEA for Johnson & Johnson's DePuy Synthes business. The specialist will lead and execute regulatory compliance activities, ensure adherence to regulations and quality standards, support audits and inspections, and partner with various teams to ensure compliant operations. The role requires experience in regulated industries and knowledge of EMEA regulatory requirements.

Johnson & Johnson is seeking a Professional Education Manager in Pomezia, Italy, to lead the design, execution, and evaluation of professional education programs for DePuy Synthes products. This role collaborates with Sales, Marketing, and Medical Affairs to support commercial strategies, manage stakeholder relationships, oversee program logistics, and ensure compliance with J&J policies and regulatory requirements. The ideal candidate has 6-8 years of relevant experience, strong project management skills, and the ability to work cross-functionally.

This role provides management and marketing support to a General Manager and local marketing team within a regulated MedTech environment. Responsibilities include calendar management, meeting coordination, operational marketing support, coordinating logistics for events, preparing marketing materials, and maintaining leadership reporting. The role requires strong administrative coordination, attention to detail, and compliance.

This role focuses on ensuring regulatory compliance for sourcing and suppliers within the healthcare industry. It involves executing compliance activities, supporting supplier qualification and lifecycle management, interpreting regulatory requirements, and preparing for audits and inspections. The role partners with Quality, Regulatory Affairs, Supply Chain, and Procurement teams.

Manager, DACH Switzerland for DePuy Synthes, a Johnson & Johnson company, responsible for leading regulatory affairs support in Switzerland, ensuring compliance with local regulatory requirements and enabling timely market access. This role involves managing regulatory risk, supporting product lifecycle activities, and partnering with stakeholders in a highly regulated environment.

The Transport Lead role at Johnson & Johnson (DePuy Synthes) is responsible for managing and optimizing international transportation operations, ensuring timely and compliant delivery of products. This involves managing logistics partners, monitoring performance metrics, ensuring regulatory compliance, and driving continuous improvement initiatives within the supply chain.

Lead Health Economics & Market Access (HEMA) strategy and execution for the Nordic countries, ensuring optimal access, funding, and adoption of innovative orthopaedic solutions. Drive value-based access strategies aligned with Nordic healthcare systems and EMEA priorities. Build and maintain relationships with payers, HTA bodies, and decision-makers. Partner cross-functionally with Marketing, Sales, Medical/Clinical, and Regulatory teams. Ensure compliance with quality, ethics, and local regulatory requirements.

Head of Government Affairs & Market Access for DePuy Synthes, a Johnson & Johnson company, located in Shanghai, China. This role shapes strategic engagement with governmental bodies, regulatory agencies, and hospital decision-makers to accelerate innovation adoption and improve patient outcomes. Responsibilities include developing government affairs strategies, monitoring policy, leading advocacy, managing market access for tendering and VBP products, overseeing health economics and evidence generation, and managing relationships with authorities for pricing and coverage decisions. The role also involves leading and developing a team, and partnering with various internal departments.

The Analyst Quality Control role at Johnson & Johnson is responsible for performing quality control tests in a pharmaceutical/biopharmaceutical setting. This includes generating test reports, ensuring compliance with GMP and other regulations, initiating and investigating quality issues, managing training, handling controlled substances, validating test methods, and performing method validation and transfer protocols. The role requires a degree in Chemistry or related field, experience in the pharmaceutical industry, knowledge of GMP and regulatory requirements, and proficiency in Microsoft Office and HPLC.

The role is for a Quality Control Analyst in the research area at Johnson & Johnson's Innovative Medicine plant in Puebla, Mexico. The position requires a degree in Chemistry or related field, 2-4 years of experience in the pharmaceutical or biopharmaceutical industry, and knowledge of GMP and regulatory requirements. Responsibilities include executing activities in EDMS, providing technical support, leading special projects, ensuring data accuracy and compliance, identifying analytical trends, escalating non-conformities, managing training, supporting regulatory submissions, executing analytical transfers, participating in audits, managing laboratory capacity, and coordinating with suppliers. The role emphasizes technical rigor, quality orientation, analytical skills, problem-solving, collaboration, and continuous improvement.

This role oversees day-to-day import and export activities within Johnson & Johnson's Supply Chain, focusing on ensuring timely issue resolution, compliance with international trade regulations, and high performance from 4PL providers and customs brokers. The position involves leading continuous improvement initiatives, developing compliant processes, partnering with various internal functions, and serving as a key interface with customs authorities and regulatory bodies. It requires strong analytical, problem-solving, and leadership skills, with a minimum of 6-8 years of experience in international trade.

Johnson & Johnson is seeking a Commercial Quality Operations Sr. Supervisor to plan, coordinate, and conduct quality programs to ensure continuous product distribution consistent with established standards. This role involves overseeing quality operations, supervising a quality team, conducting investigations, monitoring metrics, supporting supply chain quality, leading audits, and ensuring compliance with company policies, procedures, quality standards, and safety/environmental regulations. The position requires a university degree, 6-8 years of experience in a Quality Role within a GMP-controlled environment, and advanced Portuguese and English language skills.

Program Manager for Digital & Data Analytics within Johnson & Johnson's Biosense Webster division, focusing on deploying digital and data analytics solutions to support digital transformation. The role involves developing strategy, managing a team of engineers and data scientists, recruiting, mentoring, and ensuring compliance with data privacy and regulatory requirements. It also includes managing projects, budgets, and presenting insights to leadership.

Co-op position for an aspiring package engineer passionate about the healthcare industry. Responsibilities include gaining knowledge of healthcare packaging design, validation, verification, procurement, and specification development. The role involves supporting package engineering projects, understanding relevant regulations and standards (e.g., 21 CFR, ISO 11607), improving internal procedures, and interacting with suppliers. The candidate will work on projects for internationally distributed brands and manage stakeholder relationships. Requires critical thinking, problem-solving, and enthusiasm. Must be able to work full-time for 6-12 months.

Project Manager Lead for Testers & Calibration group in a Medical Device company, focusing on portfolio master planning, NPI commercialization, execution, risk management, and supply chain integration within a regulated environment.

This role is a Project/Program Management position focused on Launch Excellence for Capital and Digital solutions within the Velys Trauma & Data Products division. The Lead will manage complex projects, coordinate cross-functional teams, drive process development, and oversee data collation and insight generation to support business decisions and product launches. The role emphasizes implementing systems, automation, dashboards, and reporting tools, and guiding teams through technology project lifecycles.

The Specialist, Source-to-Contract will support the Regional Service Delivery Procurement Source-to-Contract organization by executing strategic sourcing plan implementations, sourcing and contracting cases, and other critical functional activities. This role will also support the development and implementation of automation and AI initiatives, acting as a product owner for S2C tools and AI features, gathering requirements, prioritizing, testing, and rolling out enhancements.

Senior Director of Contact Lens Quality at Johnson & Johnson, responsible for the overall strategy, execution, and oversight of quality management systems and regulatory compliance for J&J Vision Care sites. This role leads the Product Quality Lifecycle from invention to retirement, including new product design control, validation, product stewardship, supplier quality, and external manufacturing oversight. The position ensures compliance with global regulations (FDA, ISO 13485, etc.) and acts as a strategic partner to business leaders, managing budgets and developing talent within the quality and regulatory domain.

The Senior Director of Quality for Vision Equipment is responsible for the overall strategy, execution, and oversight of new product design control, validation, product stewardship, risk management, quality improvements, quality management systems, and regulatory compliance for J&J Surgical Vision sites. This role ensures compliance with FDA regulations, ISO 13485, and international requirements, acting as a strategic partner to business leaders and managing quality, safety, and compliance escalations. The position involves leading a team, managing budgets, overseeing remediation plans, and fostering a culture of compliance and talent development within the quality and regulatory compliance domain.

This role focuses on Operational Technology (OT) Cybersecurity Engineering, involving the development, deployment, and support of global OT security platforms and solutions. Key responsibilities include leading technologies, driving integration and automation, assessing risk, testing security controls, generating threat analytics, implementing detection strategies, and performing administrative tasks for security systems within IT/OT environments.

Experienced Analyst, Operational Technology Cybersecurity Engineering role at Johnson & Johnson, focusing on supporting, integrating, and automating global OT Security platforms and solutions. Responsibilities include leading technologies, driving integration, assessing risk, testing security controls, generating threat analytics, implementing detection strategies, and performing administrative tasks for security platforms. Requires hands-on scripting, OT/ICS cybersecurity expertise, strong security principles, experience with security solutions in hybrid environments, familiarity with agile/DevSecOps, and knowledge of security frameworks and the MITRE ATT&CK framework.

Johnson & Johnson is seeking a Strategic Access Manager for Hematology in Buenos Aires, Argentina. This role focuses on developing and implementing market access strategies for core products, collaborating with internal teams (Marketing, Commercial, Medical Affairs, Key Account Managers) and external stakeholders (payers, advocacy groups). Responsibilities include leading the development of technical dossiers, pricing strategies, and health economics data generation, ensuring cross-functional alignment and demonstrating product value proposition. The role requires a university degree in a relevant field, mandatory experience in Market Access and the Argentinian healthcare system, and strong analytical skills.

Principal Project Engineer responsible for managing capital projects, optimizing operational costs, and ensuring compliance with quality and safety standards within a pharmaceutical manufacturing environment. Focuses on site development, technology implementation, and process improvements.

The Service Operation Manager is responsible for the end-to-end management of Technical Service backoffice operations, ensuring operational excellence, customer satisfaction, and data-driven decision-making. This role leads all backoffice activities supporting Technical Service, including customer case management, spare parts consumption, field and depot engineer scheduling, and service execution support. The Service Operation Manager acts as a People Leader, responsible for building, developing, and engaging high-performing teams, fostering a culture of accountability, collaboration, continuous improvement, and talent development within the Service organization. In addition, this position owns the Business Intelligence (BI) strategy for the Service organization, leading data governance, dashboard and report development, and performance analysis to support both operational and strategic decisions. This role is further accountable for defining and executing the technical certification and service readiness strategy to support the implementation of service for NPIs, ensuring teams are properly trained, certified, and operationally prepared prior to market introduction. The Service Operation Manager also works closely with Sales and Marketing teams as a strategic business partner, providing service-related insights, performance data, and operational support to enable commercial strategy, customer negotiations, and business growth.

The Packaging Engineer is responsible for the management and improvement of primary and secondary packaging materials, ensuring their functionality on production lines in the manufacturing and conditioning areas. They also support operations in matters related to packaging materials. The role involves implementing plant updates for packaging material components due to design changes or regulatory updates. Responsibilities include generating material specifications, managing official packaging lists, generating material disposition forms, coordinating and executing material functionality tests, approving artwork creation, generating isometric studies, tracking quality records, coordinating change controls, ensuring project management for assigned initiatives, providing technical support for investigations and CAPAs, participating in improvement projects, and providing information during audits. The role requires a degree in a relevant scientific or engineering field, intermediate English proficiency, 1-2 years of experience in pharmaceutical, food, or chemical industries in engineering or packaging roles, and proficiency in Microsoft Office, Minitab, SAP, Project, and Visio. Knowledge of pharmaceutical regulations (NOM-059-SSA1, NOM-073-SSA1, 21 CRF 211), pharmaceutical technology, packaging technology, Six Sigma, Lean Manufacturing, statistical analysis, Design of Experiments, and advanced Minitab usage is also required.