Director, R&D Data Science, MDM Products

Johnson and Johnson Innovative Medicine (J&J IM) a pharmaceutical company of Johnson & Johnson is recruiting for a Director R&D Data Science MDM Products

This position has a primary location of Titusville NJ but is also open to Spring House PA or Cambridge MA. This position requires up to 25% travel.

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

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The Director Product Mastering is responsible for establishing and governing an end-to-end mastering capability for product-related data beginning with compounds in Therapeutic Discovery (TD) continuing through Preclinical Sciences & Translational Safety (PSTS) extending into Pharmaceutical Therapeutics Development & Supply (PTDS) and connecting seamlessly with clinical trial and regulatory data. This lifecycle mastering ensures continuity into commercial brand naming and labeling.

This role ensures that product master dataincluding compounds formulations investigational products clinical identifiers regulatory submissions and commercial brand hierarchiesis trusted harmonized and semantically consistent across the entire R&D to Commercial continuum. The Director will leverage ontologies and knowledge graphs to connect and contextualize product information across silos enabling advanced analytics AI/ML regulatory compliance and global interoperability.

Key Responsibilities

End-to-End Product Mastering Strategy

• Define and execute a mastering strategy covering the full product lifecycle: from discovery compounds preclinical entities development products (PTDS) clinical trial identifiers regulatory designations commercial brand names.

• Ensure a single authoritative source of truth for all product-related master data harmonized across functions and systems.

• Identify gaps redundancies and opportunities for automation external data partnerships and standards alignment.

Ontology & Knowledge Graph Development

• Lead the development and governance of a Product Ontology that links compounds formulations regulatory identifiers and brand entities.

• Apply knowledge graph technologies to connect product data across TD PSTS PTDS clinical regulatory and commercial domains.

• Align ontology and graph models with enterprise metadata standards and external frameworks

Governance & Standards

• Establish stewardship ownership and governance models for product master data across R&D and Commercial.

• Define and enforce standards for product hierarchies nomenclature and lifecycle transitions.

• Partner with Regulatory Affairs Clinical Operations Supply Chain and Commercial to ensure product mastering supports submission labeling and compliance needs.

Integration & Collaboration

• Collaborate with Knowledge Management Data Products and Metadata/Cataloging teams to ensure product master data is discoverable connected and reusable across the enterprise.

• Work with IT (JJT) to evaluate and implement enabling technologies for ontology graph-based integration and master data platforms.

• Align with parallel MDM domains (e.g. patient site account) to ensure cross-domain consistency.

Quality Performance & Communication

• Define and track KPIs for product master data quality timeliness and traceability across the lifecycle.

• Provide governance dashboards and reports to R&D and Commercial leadership.

• Communicate the vision progress and value realization of product mastering to senior executives and cross-functional stakeholders.

Strategic Impact

• The Director Product Mastering ensures that product-related data is connected across the full R&D-to-Commercial lifecycle. By embedding ontology-driven governance and leveraging knowledge graphs this role transforms product data into a trusted AI-ready asset that accelerates discovery supports regulatory submissions ensures compliance and strengthens commercial readiness.

Qualifications

Education

• Masters or PhD in life sciences regulatory sciences informatics data science or related field.

Skills & Expertise

• 8 years of experience in pharma/biotech R&D or commercial functions with significant exposure to product lifecycle and regulatory data.

• Demonstrated expertise in master data management ontology development and knowledge graph applications.

• Proven track record of integrating product data across discovery development clinical regulatory and commercial domains.

• Strong understanding of product data standards

• Hands-on experience with metadata management ontologies and graph-based integration technologies.

• Ability to connect scientific regulatory and commercial perspectives into a unified product mastering framework.

• Strong leadership communication and cross-functional collaboration skills.

• Ability to influence and drive adoption of product mastering practices across global organizations.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation external applicants please contact us via internal employees contact AskGS to be directed to your accommodation resource.

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