Associate Director Product Master

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Job Description:

Johnson and Johnson Innovative Medicine (J&J IM) a pharmaceutical company of Johnson & Johnson is recruiting for an Associate Director Product MasteringThis position has a primary location of Madrid Spain a secondary location is Barcelona.

Position SummaryThe Associate Director Product Mastering is responsible for maintaining and governing an end-to-end mastering capability for product-related data beginning with compounds in Therapeutic Discovery (TD) extending into Regulatory and commercialization and loss of exclusivity.

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 AD will work cross functionally within R&D Data science and support develop of ontologies and knowledge graphs to connect and contextualize product information across silos enabling advanced analytics AI/ML regulatory compliance and interoperability.

Key Responsibilities End-to-End Product Mastering Strategy

• Help to develop a data and execute a data management strategy covering the full product lifecycle: from discovery through commercialization and LOE

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

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

Governance & Standards

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

• Define and enforce standards for product hierarchies and data model extensions.

• 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.

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

Quality Performance & Communication

• Monitor dashboard 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.

QualificationsEducation

• Bachelor or Masters in life sciences regulatory sciences informatics data science or related field. Advanced degree preferred

Skills & Expertise

• 5 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 data governance and data stewardship

• Knowledge of 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 (e.g IDMP) with hands-on experience with metadata management.

• 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 functions.

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