Johnson & Johnson

Data Scientist

• Define and own the product vision, long-term strategy, and measurable business outcomes for SSOT and associated analytics platforms.
• Translate brand, and commercial priorities into a prioritized product roadmap, backlog, release plan, and adoption roadmap.
• Partner with GCSO across TAs, Data Science, Technology, and platform leadership to ensure roadmap alignment with business performance objectives and enterprise architecture direction.
• Maintain a transparent roadmap governance model that balances new capabilities, technical debt, compliance needs, user adoption, and operational excellence.
• Serve as the interface between business owners including Global Commercial Insights leads across TA, PICs & PM Teams, DSI, RWE Global Council, and technology delivery teams, engineering & platform operations to strengthen the global launch excellence capabilities.
• Gather, rationalize, and translate business requirements into actionable product features, analytics use cases, acceptance criteria, and adoption plans.
• Facilitate regular stakeholder engagement, roadmap reviews, prioritization forums, and executive readouts to ensure alignment, transparency, and timely decision-making.
• Ensure platforms deliver timely, scalable, governed, and reproducible insights that support commercial decision-making and portfolio performance management.
• Oversee implementation of data pipelines, automation, feature engineering, analytics frameworks, dashboards, and reusable data products.
• Partner with Data Science Chapter leads to drive adoption of AI/ML-enabled insights, AI-enabled conversational analytics, and advanced analytics capabilities that improve decision quality and business agility.
• Govern the end-to-end analytics platform ecosystem, including data ingestion, transformation, storage, semantic layers, visualization, and consumption patterns across platforms.
• Maintain data quality, lineage, governance, privacy, access controls, and role-based security.
• Enable actionable insights across disease landscape, patient journey, market trends, share, performance metrics, launch readiness, and product lifecycle performance.
• Lead agile product delivery across backlog prioritization, sprint planning, dependency management, release readiness, change management, and post-release adoption tracking.

Senior Manager, Data Science

Risk

• Actively and independently participates in all study activities, contributing to the identification and assessment of key risks in the clinical protocol/set-up and advising clinical team members on effective mitigation strategies for complex clinical trials, compounds and programs.
• Leads regular review of risk areas in collaboration with Risk Owners, to evaluate progress of risk mitigations and risk reduction, and to identify potential new risks or additional mitigation needs (trial and/or compound, as assigned).
• Maintains CQP (Clinical Quality Plans) in quality repository to facilitate regular progress reviews of quality support services in addition to risks and mitigations.
• Independently drives quality risk monitoring reviews and coaches others on risk monitoring and mitigation reviews.
• Communicates and facilitates risk updates to R&D colleagues as part of the regular review cycle through Quality Working Groups and Governance Fora, as applicable (trial and/or compound, as assigned).
• Highlight new potential systemic risk to RDQ CRM management.
• Develops and ensures a consistent interpretation of issues that require quality investigations.
• Provides guidance for significant quality issues (SQI) per corporate standards and escalates SQI to senior R&D management.
• In collaboration with partners in RDQ, provides advice on the development and implementation of Corrective and Preventative Action (CAPA) Plans and Effectiveness Checks (Self - Identified, Inspection, Audit).
• Drives ongoing inspection readiness activities with trial teams to develop inspection narratives, identify and prepare sites of interest for inspection (including, pre-inspection visit support), ensure availability of key documents/records and coordinates mock inspection in collaboration with Regulatory Compliance teams.
• Provides support for Investigator, Sponsor-Monitor and third-party inspections including post inspection support.
• Provides independent advice on questions related to research quality and compliance from clinical teams in collaboration with other Quality Professionals and Subject Matter Experts to ensure consistent interpretation of international regulations and policy.
• Participates in Clinical risk Management, cross R&D quality, cross functional and cross sector working groups to develop or refine processes, tools, and systems that deliver innovative quality solutions.
• Provides training and coaching to peers and new employees, as needed.

Associate Director, Cross TA Risk Management

Consultant

• Train, educate, and support combined CT/Heart Failure programs on the proper use of the Impella
• Full customer immersion within 5.5 sites to ensure optimal patient outcomes
• Internal collaboration with the Surgical Leadership Team, Training Team, Engineering Team, Marketing, Professional Education, Clinical, as well as with R&D
• Perform device training on full Impella Device line-up
• Cultivates close relationships with strategic business partners and key opinion leaders

Advanced Surgical Consultant – Heart Recovery

Clinical Operations

• Own vision, priorities, and near-term roadmap for participant data collection capabilities in alignment with Clinical Operations objectives, business impact, and study delivery needs.
• Shape and prioritize the squad backlog by translating Clinical Operations needs, study process requirements, and customer insights into clear user stories and acceptance criteria.
• Balance business value, customer experience, and technical feasibility while prioritizing features, enhancements, fixes, and release content.
• Act as the voice of the customer within the squad to help ensure solutions meet user needs across Clinical Operations, study teams, sites, and participant-facing processes.
• Work closely with engineering, UX, data management, privacy, security, quality, and compliance stakeholders throughout the product lifecycle.
• Facilitate release planning, sprint planning, reviews, demos, and synchronization with dependent teams to support delivery across cross-squad and operational workflows.
• Track squad-level metrics and operational results to provide visibility into adoption, delivery performance, data quality, and user outcomes.
• Work with the Lead Engineer to assess solution options, support user testing readiness, and balance technical debt with feature delivery.
• Support communications, training, documentation, and stakeholder engagement to improve adoption, clarity on roadmap activities, and release readiness.
• Actively participate in squad ceremonies and continuous improvement activities to help optimize the flow of value and delivery efficiency.

Technical Product Owner, Clinical Operations Technology

Manager

• Drive operational excellence of product escalations and field action processes under applicable J&J procedures and regulatory requirements.
• Manage MedTech Surgery team responsible for scheduling, coordination and preparation of Product Issue Escalation and Quality Review Board (QRB) Meetings.
• Oversight of the department’s budget, hiring, retaining and developing qualified personnel, as well as resolving all personnel issues and employee performance management.
• Provide support to internal and external audit processes.
• Serve as SME in responsible areas for internal and external audits.
• Monitor key process metrics for product issue escalation and field actions, communicate status and identify opportunities for process improvements across MedTech organizations.
• Support OUS affiliates, with monitoring field action reporting through action closure, identifying process improvements to ensure timeliness closures.
• Establish and maintain policies and procedures to ensure compliance with local, state and federal environmental regulations and standards including compliance with all Food & Drug Administration (FDA) and European Union Medical Device Directives (MDD)/European Union Medical Device Regulation (MDR) as well as all other applicable global regulatory requirements.
• Act as a representative for J&J Medical Devices to US FDA, worldwide health authorities and notified bodies, as applicable.
• Communicate business-related issues or opportunities to next management level.
• Manage field corrective actions, any associated regulatory actions and follow-ups; lead in product problem resolution as part of follow-up from QRB and CAPA.
• Oversee technology platform supporting the product issue escalation, quality review board, and field action processes to ensure compliance to regulations and standards and effective internal process flow.
• Participates and stays well-informed of enterprise solutions and their impact to emerging field action and product quality escalation internal and external standard changes.
• Establishes and maintains training programs to execute field actions with required stakeholders to effectively determine product quality issue resolution.
• Responsible for communicating business related issues or opportunities to next management level.
• For those who supervise or manage staff, responsible for ensuring that subordinates follow all company guidelines related to health, safety and environmental practices and that all resources needed to do so are available and in good condition, if applicable.
• Responsible for ensuring personal and company compliance with all federal, state, local and company regulations, policies, and procedures.
• Perform other duties assigned as needed.

Senior Manager – Field Action & Escalation

Director

• Provide enterprise leadership for the strategy, roadmap, operation, and sustainment of core QMS systems and enabling platforms
• Partner closely with Innovative Medicine Quality & Compliance, Enterprise Quality, IM Digital Quality, JJT, Global Process Owners, and regional stakeholders to ensure QMS systems support business priorities, regulatory expectations, inspection readiness, and continuous improvement
• Lead global QMS system strategy, business ownership, system investment planning, and operational services, including support for Transcend, QMS Operations, LMS, EDMS, and related QMS workflows
• Provide strategic direction, people leadership, governance, and stakeholder engagement to advance a scalable, compliant, and digitally enabled QMS ecosystem
• Oversee planning, execution, sustainment, and continuous improvement of QMS system initiatives and investments
• Serve as business owner for core QMS systems and enabling platforms, including LMS, EDMS, QMS workflows, and related operational capabilities
• Develop scalable operational services and support models that enable consistent, efficient, and compliant QMS operations
• Represent IM Quality Systems in enterprise transformation efforts, governance forums, and senior leadership discussions
• Monitor internal and external trends in Quality Systems and digital capability to identify opportunities for simplification, standardization, innovation, and value creation
• Develop dashboards, metrics, and leadership updates to provide visibility into QMS system performance, investment progress, risks, and opportunities

Senior Director, Quality Systems

Vice President

• Lead global process ownership and governance for enterprise Quality processes
• Define and maintain global process standards, procedures, roles and responsibilities, governance forums, and performance expectations
• Partner with cross-functional leaders to align Quality process strategy with business priorities, regulatory expectations, and operational needs
• Lead simplification, harmonization, and continuous improvement initiatives
• Provide strategic leadership for digital Quality systems and eQMS optimization
• Establish and monitor global Quality performance metrics, dashboards, and management review mechanisms
• Support regulatory inspections, audits, and remediation activities
• Lead global councils, communities of practice, and change-management efforts

VP Global Process Management

Account Executive

• Meet or exceed sales expectations within assigned geographies in an ethical and compliant manner
• Understand and identify customer needs, aligning marketing resources and supporting pull-through activities
• Embody and communicate Intra-Cellular’s corporate vision
• Develop superior product and disease state knowledge
• Engage in in-depth clinical dialogue with healthcare professionals
• Create local strategic and tactical plans
• Provide effective application of budget and expense management within assigned territory
• Collaborate with other Neuroscience Sales Specialists on common objectives
• Provide timely and accurate administrative management of work hours, sales call data, and customer objectives
• Complete all company and job-related training as assigned within required timelines

Neuroscience Sales Representative

• Define and execute the global benefits strategy aligned to enterprise, talent, and Total Rewards priorities
• Oversee design of health, retirement, risk, wellbeing, leave, and ancillary programs across regions balancing global consistency with local market relevance.
• Establish global standards, governance frameworks and policies while ensuring compliance with global, regional, and local regulatory requirements and standards.
• Partner with senior HR, Finance, Legal, and business leaders to align benefits strategy with workforce and business needs.
• Lead vendor strategy, including selection, performance management, and optimization of benefits providers and advisors.
• Leverage analytics and benchmarking focusing on program competitiveness and innovation, cost and risk management and positive employee experience
• Lead, develop, and engage a high-performing global benefits team.
• Lead M&A benefits strategies and implementation (due diligence, integration of benefits programs)
• Drive clear, effective benefits communication and engagement strategies ensuring programs are understood, accessible and valued by employees
• Identify and implement innovative solutions that simplify processes, improve market competitiveness, and enhance employee experience and cost effectiveness.

Senior Director, Global Benefits – Orthopedics

General

• Acts as a scientific expert and implements Medical Affairs product plans
• Proactive and reactive scientific engagement with external experts
• Communicates on-label product data and discusses clinical study programs
• Responsible for planning and conducting pipeline and strategy meetings
• Supports the design, planning, and execution of clinical trials
• Coordinates collaboration with clinical trial sites
• Identifies needs for medical education activities
• Responsible for scientific representation at congresses and events

Senior Medical Science Liaison – Hematology

• Acts as a scientific expert and implements Medical Affairs product plans within the region
• Engages in proactive and reactive scientific exchange of medical and scientific information with external experts
• Communicates in-label product data and discusses clinical trial programs
• Responsible for planning and conducting pipeline and strategy meetings
• Develops in-depth strategic knowledge of treatment pathways and contributes to identifying outstanding core questions
• Supports the setup, planning, and execution of clinical drug studies
• Coordinates collaboration with study sites in alignment with MAF ID/GCO
• Identifies needs for Medical Education activities and conducts these initiatives
• Participates in scientific discussions and is responsible for the Company’s scientifically excellent representation at congresses

• Acts as a scientific expert
• Implements Medical Affairs product plans
• Proactive and reactive scientific exchange with external experts
• Communicates product data and discusses clinical study programs
• Responsible for planning and conducting pipeline and strategy meetings
• Supports identification of potential study sites and the development of partnerships
• Coordinates collaboration with study sites
• Identifies needs for medical education activities

• Acts as a scientific expert and implements Medical Affairs product plans
• Proactive and reactive scientific exchange of medical and scientific information with external experts
• Communicates on‑label product data and discusses clinical study programs
• Responsible for planning and conducting pipeline and strategy meetings
• Identifies outstanding core questions and medical needs for the development of patient outcome solutions

Sr. Medical Science Liaison – Hematology

• Own the technology and its future! Develop and routinely update the global strategy and roadmap for the designated manufacturing process, considering external market, competitor, and technology trends.
• Drive global process excellence by ensuring that process changes and improvements are effectively communicated and adopted across all manufacturing sites.
• Establish and maintain global validation strategies and support relevant audits specific to the process, fostering continuous improvement and compliance.
• Act as the go-to expert for all technical aspects of Machining processes across all sites, with an unparalleled understanding of the existing process and the opportunities that can be harnessed to drive step-change improvements.
• Approve and endorse process changes, including new equipment, upgrades and modifications, ensuring compliance with internal standards and regulatory requirements.
• Provide technical support and governance on existing initiatives within the business, working collaboratively with cross-functional teams to resolve challenges and streamline operations.
• Work collaboratively with the business to ensure that it has the investments, infrastructure, capital and talent required to implement the technology strategy and roadmap.
• Support the development of new programme charters and initiatives by providing expert guidance on timelines, costs, risks, and benefits during development and implementation of new innovations.
• Collect, analyze, and report metrics related to the process, such as performance trends, aligning these insights with overall business metrics.

Global Process Owner – Machining, Finishing

• Supporting chamber monitoring readiness, Yokogawa panel replacement activities, change control execution, and financial planning within Biologics AD.
• Ensuring operational continuity, compliance, timely record management, and sound budget oversight through close collaboration with facilities, quality, finance, project management, and site stakeholders.
• Maintaining and verifying chamber monitoring tracking information and confirming readiness for routine and quarterly monitoring activities.
• Reviewing and supporting change controls related to chamber updates and Yokogawa panel replacements, including coordinating assessments, approvals, and communication of monitoring gaps.
• Partnering with chamber owners, facilities, and service providers to support monitoring readiness, equipment status, and required documentation.
• Serving as a business lead and subject matter resource for COMET change control processes, including supporting user adoption, issue resolution, system testing, process improvements, and stakeholder communication.
• Acting as a single point of contact for assigned change controls, including pre-change planning, record assignment, assessment initiation, follow-up, board review coordination, approvals, extensions, amendments, and closure tracking.
• Maintaining reports, dashboards, and periodic updates for change controls, NC/CAPA activities, investigations, action items, and compliance metrics.
• Supporting monthly financial close and reporting activities, ensuring accurate and timely financial information.
• Developing and managing capital and expense budgets, forecasts, scenario planning, and variance analyses.
• Monitoring project performance against forecasts, updating budgets during planning cycles, and supporting on-time, within-budget execution.
• Building dashboards, analyzing performance trends, and providing insights to support financial, operational, and strategic decision-making.
• Collaborating with Finance, Operations, PMO, Supply Chain, Quality, and scientific teams to improve planning, controls, standardization, and execution.

Senior Manager, Data Science

Associate Director, Cross TA Risk Management

Advanced Surgical Consultant – Heart Recovery

Technical Product Owner, Clinical Operations Technology

Senior Manager – Field Action & Escalation

Senior Director, Quality Systems

VP Global Process Management

Neuroscience Sales Representative

Senior Director, Global Benefits – Orthopedics

Senior Medical Science Liaison – Hematology

Senior Medical Science Liaison – Hematology

Senior Medical Science Liaison – Hematology

Sr. Medical Science Liaison – Hematology

Global Process Owner – Machining, Finishing

Scientist, Biologics Analytical Development – Proteins