Senior Financial Manager for Global Digital Transformation in MedTech Supply Chain at Johnson & Johnson. Role focuses on financial leadership, transformation program valuation, long-range financial planning, strategic decision support, and managing a team. Key responsibilities include partnering with leadership, driving process improvements, governing financial planning cycles, overseeing financial closing, tracking value realization, and team leadership. The role aims to AI-enable planning and deliver predictive insights.

This role supports the global deployment of Quality Management (QM) capabilities within the Transcend SAP S/4HANA program. It ensures integration with NextGen QS for real-time control and disposition of non-conforming materials and batches across Source, Make, and Deliver. The role owns the end-to-end implementation of Quality processes for release management, laboratory testing, manufacturing batch record review, and artwork key date management. It also defines and deploys batch determination rulesets to ensure compliant batch usage and shipment. The role involves functional ownership, leadership, solution delivery, testing, hypercare, and cross-functional collaboration with various teams including IT, Validation, and Quality Assurance.

This role is a Senior Clinical Account Specialist for Johnson & Johnson MedTech, focusing on Electrophysiology. The primary responsibilities include providing expert clinical product and technical assistance, training physicians and EP Lab Staff on electrophysiology systems during procedures, educating customers on product usage, identifying sales opportunities, and building customer relationships. The role also involves administrative tasks and ensuring compliance with company guidelines and regulations.

This role focuses on product safety analysis and risk management within the healthcare domain, specifically for Johnson & Johnson's Innovative Medicine division. The Associate Director, Safety Analysis Scientist will provide scientific expertise, lead safety assessments, prepare scientific evaluations for regulatory compliance, and collaborate with cross-functional teams to determine safety strategies and interpret safety information. The role involves proactive review of safety data, support for Health Authority interactions, and exploring innovative ways to present data, but it does not involve the core craft of building or deploying AI/ML models.

This role is for an Associate Director, Safety Analysis Scientist at Johnson & Johnson, focusing on product safety assessment and risk management within the healthcare domain. The position involves leading safety evaluations, preparing scientific safety analyses for regulatory compliance, collaborating with cross-functional teams, and supporting safety management teams. The role requires in-depth product knowledge, independent decision-making, and proactive review of safety data. It is not directly involved in AI/ML model development or deployment.

This role provides scientific expertise and leads the safety assessment of assigned products, preparing scientific safety analysis and evaluations for regulatory compliance and safety-related decisions. It involves supporting Safety Management Teams, collaborating with cross-functional partners, reviewing safety data, and providing input on key safety and clinical documents. The role requires in-depth product knowledge, leadership in SMTs, and support for Health Authority interactions.

Johnson & Johnson Innovative Medicine is seeking a Medical Science Liaison for their Autoantibody Pipeline in the Southeast region. This field-based role involves providing scientific and clinical information to healthcare professionals and opinion leaders, staying updated on therapeutic areas, and supporting research initiatives. The MSL will build external relationships, develop territory strategic plans, and ensure all activities comply with regulatory and healthcare guidelines. The role requires a strong understanding of the disease state and competencies in communication, stakeholder engagement, and data dissemination.

Production Associate II role at Johnson & Johnson's Orthopedics division in Grecia, Costa Rica. Responsibilities include carrying out operations as per CSOPs, maintaining production and quality records, operating within a cellular manufacturing environment, maintaining GMP/Housekeeping standards, processing product to output and quality standards, working in an environment of continuous change, assisting in audits, adhering to company policies and HSE procedures, and safe operation of equipment like CNC Machines. The role also involves communicating business issues, ensuring compliance with regulations, and training fellow associates.

Senior Manager, Global Trade Controls, APAC for Johnson & Johnson, focusing on implementing global import & export controls strategy, providing regional guidance on trade regulations, and leading a team of trade professionals in the APAC region.

Johnson & Johnson is seeking a Field Enablement Manager to drive effectiveness and performance of their field team by delivering strategic training, resources, and tools. This role involves developing and implementing training programs, collaborating with marketing to disseminate content, traveling to field locations, and serving as a liaison between the field and corporate support. The ideal candidate will have a Bachelor's degree (Master's preferred), 6+ years of experience in field clinical enablement or sales within the cardiology/cardiac surgery medical device industry, strong communication and project management skills, and enhanced analytics skills.

Product Manager for Software roadmap for capital systems and instruments in MedTech Surgery, focusing on new product development, launch excellence, market research, business case development, R&D collaboration, and go/no-go decisions. The role involves managing SW roadmaps, identifying and prioritizing features, coordinating translations, exploring algorithm opportunities, and collaborating with cross-functional teams for go-to-market execution and product support. Responsibilities include managing dependencies, risks, budget, timelines, driving operational excellence, monitoring development progress, implementing post-launch activities, and leading customer validation efforts.

The Global Training Leader at Johnson & Johnson is responsible for developing and implementing training strategies for the production organization, managing a global team of trainers, and collaborating with production, engineering, and quality teams to meet business objectives. This role involves managing training initiatives, budgets, and vendor relationships, and ensuring training solutions support yield improvement and scrap reduction.

Senior Manager, Customer Insights for the Biosurgery platform at Johnson & Johnson MedTech Surgery. Responsibilities include owning the customer insights strategy, managing primary and secondary market research, market analytics, and translating research into actionable recommendations for pipeline strategy, portfolio prioritization, and launch readiness. The role also involves developing forecasting models and managing vendor relationships.

Principal Quality Engineer (Design Assurance) for a medical device company (Shockwave Reducer) focused on ensuring medical devices are designed, developed, and transferred to manufacturing in compliance with quality system and regulatory requirements. Responsibilities include leading quality assurance for new product development, partnering with R&D and other teams, managing risk, overseeing V&V, supporting design transfer, and participating in regulatory audits and submissions.

This role is a Senior Thought Leader Liaison for Multiple Myeloma within Johnson & Johnson's Oncology division. The primary focus is on leading regional Key Opinion Leader (KOL) engagement strategies, developing marketing education plans, and building relationships with KOLs to support brand advocacy and market insights. The role involves understanding industry trends, managing budgets, and potentially managing other liaisons, all within a regulated healthcare environment.

Executive Oncology Sales Specialist for Solid Tumor at Johnson & Johnson Innovative Medicine, responsible for fulfilling sales strategies, demonstrating product knowledge, articulating value propositions, providing clinical support, and achieving sales objectives within the Nashville, TN territory. Requires a bachelor's degree, 2+ years of sales experience in pharmaceuticals, biologics, or medical devices, and experience in hospital/large account sales with reimbursement knowledge.

This role supports the sales organization by managing operational aspects of digital surgery offerings, specifically VELYS Trauma products. Responsibilities include monitoring expirations, ensuring compliance with contracting and billing, maintaining master contract and billing files, detecting discrepancies, and providing insights to support business decisions. The role also involves collaboration with various internal teams and external customers.

Johnson & Johnson MedTech, Neurovascular is seeking a Regulatory Affairs Specialist II to support regulatory activities for obtaining and maintaining medical device approvals/clearances in the US and European markets. This role involves preparing, submitting, tracking, and archiving official documents and files, and collaborating with various internal and external partners.

This role is for an Associate Medical Director in US Medical Affairs focusing on Autoantibody Neuroimmunology within Johnson & Johnson's Innovative Medicine division. The position involves developing and executing the Therapeutic Area strategic plan for Medical Affairs, which includes designing and managing registries, Phase IIIb/IV trials, and post-marketing requirements. The role requires influencing product development, scientific communication, and evidence generation, collaborating with various internal teams and external experts, and contributing to regulatory submissions and interactions. The Associate Medical Director will serve as the Study Responsible Physician for clinical programs, ensuring alignment with business objectives and regulatory standards.

This position is responsible for maintaining the reliability of manufacturing assets and utilities through preventive, corrective and calibration workorders, and parts storeroom management. Supervise daily maintenance activities of technicians and contractors in clinical manufacturing, labs, utilities and facilities. Ensure safe work and high levels of schedule attainment and resource utilization. Participate in planning and scheduling of work. Maximize engagement and performance of your team through effective leadership, communications and administration of the Performance and Development Process. Ensure that all work is completed safely and cost-effectively and in compliance with Company Policies, EHS guidelines and GMP’s (Good Manufacturing Practices).

Associate Regional Sales Manager for Johnson & Johnson's DePuy Synthes Trauma portfolio, responsible for leading sales strategies, operations, and budgets to drive sales growth and achieve objectives in the North Houston area. The role involves implementing selling strategies, demonstrating product knowledge, recruiting and developing sales professionals, managing business expenses, and building relationships with key stakeholders in the healthcare industry.

This role is for a Physician Program Director in the MedTech Sales division at Johnson & Johnson, focusing on establishing and managing formal Impella programs through relationships with account stakeholders and Key Opinion Leaders (KOLs). The role involves engaging KOLs, developing strategic relationships, and acting as a liaison between hospitals and internal company resources. It also includes collaborating with hospitals on program efficiencies, best practice implementation, and workflow improvements to ensure program sustainability. The PPD will work to identify program gaps, align internal resources, and support the implementation of best practices across hospital systems. The role requires understanding hospital market dynamics, presenting complex health economic information, advocating for heart recovery programs, and developing new KOLs. It also involves serving as a corporate liaison and collaborating cross-functionally with internal partners. The position requires extensive travel and a strong understanding of US healthcare policy and payment systems.

This role is for an Experienced Analyst focused on Customer Excellence within the Transcend program at Johnson & Johnson. The program aims to modernize foundational transactional processes and harmonize them into a single ERP system. The analyst will provide advanced support for order management and Customer Excellence processes, including functional analysis, interface validation, testing, and deployment support within a GxP-regulated environment.

The Physician Program Director (PPD) role at Johnson & Johnson's MedTech division focuses on establishing and managing formal Impella programs within hospitals. This field-based position involves developing strategic relationships with Key Opinion Leaders (KOLs) and account stakeholders to support scientific, medical, and commercial goals. The PPD will collaborate with hospitals to improve program efficiencies, implement best practices, and develop protocols for long-term sustainability. Responsibilities include understanding hospital market dynamics, presenting health economic information, advocating for heart recovery programs, identifying emerging KOLs, and acting as a liaison between KOLs, hospital leadership, and internal J&J teams (medical office, research, marketing, sales, executive). The role requires extensive travel and a strong understanding of US healthcare policy and reimbursement systems.

Product Manager for Surgical Vision EMEA portfolio and life cycle management, focusing on LCM and NPI commercial operations for IOL, OVD, and Equipment portfolios. Responsibilities include executing LCM strategies, managing regional launch plans, creating customer communications, setting NPI pricing, managing marketing materials, reducing inventory, obtaining regulatory approvals, and collaborating with cross-functional teams.

Apprentice Manufacturing Technician role focused on operating and monitoring processing equipment (injection molding, extrusion) for contact lens production, conducting quality inspections, gathering production data, performing maintenance, and troubleshooting issues within a regulated healthcare manufacturing environment.

Johnson & Johnson MedTech is seeking a Service Performance Sr Manager, Service Innovation to support the Service organization in Japan. This role involves establishing collaboration between Japan and USA Service organizations, developing service processes and infrastructure, and contributing to the Service product roadmap. The position requires experience in DFX, designing for Serviceability, and understanding of product creation processes within a regulated environment.

This role focuses on managing user access security and compliance within global SAP S4 HANA & ECC systems. It involves supporting SAP security applications, investigating incidents, maintaining a secure environment, and managing role changes. The position requires experience in SAP security administration, GxP & SOX compliance, and SAP authorization concepts.

The Associate Regulatory Affairs Specialist will support regulatory activities for medical device approvals in the US and European markets. This role involves preparing, submitting, tracking, and archiving regulatory documents, and collaborating with various internal departments and external regulatory agencies. The position requires understanding of global regulatory processes and compliance with relevant standards like ISO 13485.

Entry-level Associate Manufacturing Operator at Johnson & Johnson in Leiden, Netherlands. This role supports manufacturing operations by executing defined tasks, following standard procedures, and ensuring accuracy and quality of deliverables. Requires an MBO-2 degree with relevant experience or a non-relevant MBO-2 degree with more experience, basic Dutch or English proficiency, and flexibility for shift work. Focuses on GMP compliance and process adherence.

The EAMA Manager role at Johnson & Johnson in Beijing, China, focuses on market access and reimbursement within the healthcare sector. The position requires in-depth research and analysis of national and local medical insurance policies, tracking trends, and assessing their impact on the medical device industry. The manager will develop company strategies for medical insurance, identify market opportunities, manage policy risks, conduct internal policy training, and engage with government affairs and relevant authorities. Collaboration with industry associations, experts, and partners is also key to building a long-term policy environment. The role requires a Master's degree or higher in public health, medical insurance management, or pharmaceutical policy, with experience in government affairs, policy research, or market access within the medical device or pharmaceutical industry. Strong policy analysis, research report writing, strategic planning, communication, and cross-functional collaboration skills are essential. Fluency in English is also required.

Johnson & Johnson is seeking a Territory Manager for their Shockwave IVL portfolio in Sweden. The role involves training and educating end-users, maintaining customer relationships, driving sales, and providing case coverage in catheter labs. The ideal candidate will have experience in the medical device market, particularly in interventional procedures, and possess strong commercial and communication skills.

The Sr Manager Quality Systems & Quality Excellence will lead and manage a team responsible for quality processes within the J&J Innovative Medicine Supply Chain. This includes managing GMP training, document management, and narcotic compliance. The role focuses on ensuring compliance, identifying areas for continuous improvement, and serving as a Quality Systems expert. Responsibilities include integrating reporting and analytical tools, maintaining performance monitoring systems, transforming data into insights, and representing Quality Systems on various committees. The role also involves leading the Narcotics Compliance team to ensure compliance with legal requirements for controlled substances.

Johnson & Johnson is seeking a Junior Data Engineer to join their technology team. The role focuses on designing, developing, and maintaining a Data Lakehouse architecture on AWS Cloud using Databricks and Tableau. Responsibilities include data ingestion, transformation, storage, ensuring data quality, and collaborating with cross-functional teams. The ideal candidate will have a background in software development, data engineering, cloud technologies, and experience with programming languages like Python and data processing frameworks.

Technology Leader for Heart Recovery in the APJ region, responsible for driving regional technology strategy, demand shaping, portfolio management, budget oversight, and delivery of solutions across Commercial, Supply Chain, and R&D. This role requires self-sufficiency, relationship building, and ensuring solutions align with global standards while meeting regional business outcomes.

Technology Leader for Heart Recovery in APJ region, responsible for driving regional technology strategy, demand shaping, portfolio management, budget oversight, and delivery orchestration across Commercial, Supply Chain, and R&D. This role requires strong self-sufficiency, stakeholder leadership, and experience in a matrixed, cross-geography environment, ensuring solutions meet business outcomes and compliance standards.

Senior Regulatory Affairs Specialist role focused on medical device submissions and compliance with EU regulations, specifically for cardiovascular devices. Requires experience with MDR (EU) 2017/745 and supporting product lifecycle regulatory strategies.

Manager, Procurement EMEA Travel & Meetings role at Johnson & Johnson, responsible for developing and implementing TME category strategies in the EMEA region, managing spend of approximately $280 million, and ensuring adherence to policy and cost savings. Requires strong business acumen, stakeholder engagement, and supplier relationship management.

This role is a Quality Specialist for Service & Repair in the Orthopedics division of Johnson & Johnson, focusing on ensuring compliance and quality standards for EMEA Service Centers. Responsibilities include managing quality and compliance aspects, supporting validation of equipment and computer systems, supplier management, collaborating with various teams on process harmonization and complaint handling, tracking performance metrics, coordinating non-conformance resolution, supporting audits, and leading continuous improvement initiatives within a regulated ISO 13485 environment.

This role provides regulatory affairs support for a business separation project (Project Osprey) in Hong Kong. Responsibilities include managing regulatory activities, license transfers, tender support, new registrations for specific regulated products (bone matrix and radio frequency equipment), and authority interactions to ensure business continuity during the transition to a new legal entity. The role requires experience with Hong Kong regulatory authorities and medical device regulations.

Johnson & Johnson MedTech Cardiovascular is seeking an LCM System Engineer to manage the full lifecycle of Testers & Calibration systems, including EOL processes, upgrades, and improvements. The role involves leading POD activities for hardware, software, and process updates, developing production support systems, and driving Cost Improvement Projects (CIP) to enhance yields, quality, efficiency, and cost-effectiveness. The position requires a B.Sc. in Engineering, minimum 3 years of experience as a System Engineer, strong electronics knowledge, debugging capabilities, and basic software understanding. Experience in manufacturing support, particularly in medical devices, is an advantage.

Lead a multidisciplinary systems engineering team and provide technical and organizational leadership for a complex surgical robotic platform across its full product lifecycle. Ensure cohesive system behavior across hardware, software, controls, and clinical workflows, applying rigorous systems engineering principles to a safety-critical medical robotic system. Partner with commercial, clinical, and product management stakeholders to translate clinical user needs, surgeon workflows, and business objectives into well-defined system requirements and successful new product introductions. Ensure customer, clinical, and regulatory expectations are effectively decomposed into robust, traceable system and subsystem solutions. Lead the end-to-end requirements flow-down process, starting with identification and engagement of clinical and business stakeholders, definition of user and system requirements, development of system architecture, and decomposition into clear, testable subsystem requirements. Drive alignment between system architecture decisions and downstream implementation to ensure performance, safety, reliability, and usability objectives are met. Play a critical role in regulatory submissions and product releases by leading the planning, execution, and documentation of design control activities in compliance with FDA regulations, ISO 13485, IEC standards, and other applicable regulatory and quality system requirements. This includes ownership of system-level risk management, requirements traceability, verification strategies, and design reviews. Requires close and continuous collaboration with electrical engineering, software, controls, mechanical engineering, clinical, quality, manufacturing, and verification & validation (V&V) teams. Ensure cross-functional integration, resolve technical trade-offs, and drive system-level decision-making across disciplines to deliver a cohesive, compliant, and high-performing robotic system.

This role is a Product/Marketing Manager for minimally invasive surgical procedures in cardiothoracic surgery at Johnson & Johnson. It focuses on promoting new techniques, building adoption, and collaborating with experts and societies to establish industry consensus and execute strategies. The role requires strong execution, communication, and healthcare industry experience.

The Senior Learning Delivery Analyst coordinates day-to-day end-to-end learning delivery operations, including learning setup and assignments, user group administration, and reporting within the Learning Management System (LMS). This role also manages learning logistics such as room bookings, coach availability and assignments, materials coordination, and catering to ensure seamless and effective learning delivery. The role involves managing course setup, logistical activities for events, conducting post-event reviews, providing data and reporting, directing analysts, establishing partnerships with key contacts, adopting and promoting the use of tools/systems, documenting processes, and ensuring compliance with relevant laws and regulations.

Sales Manager for a medical device (Heart Recovery - Impella) in South East Asia, focusing on leading a clinical and sales team, driving adoption, providing clinical guidance, conducting training, building networks, managing accounts, representing the company at conferences, and managing distributor relationships. Requires extensive experience in healthcare, clinical leadership, and working with Key Opinion Leaders.

The AskGS Experience Center Associate - German Bilingual will provide customer service support for HR, Procurement, and Payroll processes and policies through various communication channels. This role involves resolving inquiries, documenting cases, escalating complex issues, and promoting self-service options. The associate will also contribute to process improvement and knowledge sharing within the Global Services team.

Operations Team Lead at Johnson & Johnson's Orthopaedics division in Blackpool, UK. The role involves day-to-day supervision and leadership on the shop floor, managing resources, ensuring compliance with safety, environmental, and quality standards, and driving operational excellence. Responsibilities include production output tracking, mentoring, resource allocation, problem-solving, performance management, and promoting continuous improvement using Lean methodologies within a regulated manufacturing environment.

Product Director role focused on marketing and community expansion for bispecific oncology drugs (TECVAYLI and TALVEY). Responsibilities include developing marketing content and programs to address adoption barriers, shaping and implementing external partnerships and educational programs, leading pharmacist market development, and supporting existing educational programs. Requires a Bachelor's degree, 7+ years of business experience (including pharma/healthcare), and 5+ years in sales, marketing, or related fields. Experience in oncology or with new treatment modalities is preferred.