Product Data Officer (Hybrid) — Medical Devices

IQVIA; Madrid; Presencial; EUR 21.000 - 32.000; Jornada completa

Descripción de la vacante

IQVIA is seeking 8 Product Data Officers to join the Product Reference Team in Madrid. This 6-month temporary position focuses on creating, maintaining, and enhancing the Global Medical Devices Product Reference Database, ensuring high data quality and consistency across sources.

You will classify, standardise, and group products per business rules, while collaborating with Governance and Business teams to improve reference data structures and processes in a dynamic, multicultural environment.

Formación

• Bachelor's degree or equivalent in a related field.
• Industry knowledge of Medical Devices products and classifications is valued.
• Advanced English; other European languages (French, German, Italian) are a plus.

Responsabilidades

• Identify and validate equivalent product records across multiple data sources.
• Create, update, and maintain Medical Devices product reference data.
• Classify, standardise, and group products according to rules and hierarchies.
• Conduct product research using internal and external sources.
• Utilise AI and digital tools to collect, structure, enrich, and analyse product information.
• Review AI-generated content for accuracy and compliance.
• Analyze product data to identify enhancements and process improvements.
• Detect and correct inaccurate or duplicate records.
• Investigate and resolve routine data issues.
• Perform quality control to ensure data integrity.
• Maintain process documentation and procedures.
• Identify automation opportunities to improve data quality.

Educación

Bachelor's Degree Or Equivalent Qualification, Preferably In Life Sciences

Life Sciences

Biomedical Engineering

Health Sciences

Data Analytics

Information Management

Or a related discipline

Descripción del empleo

IQVIA is seeking 8 Product Data Officers to join the Product Reference Team in Madrid. This 6-month temporary position focuses on creating, maintaining, and enhancing the Global Medical Devices Product Reference Database, ensuring high data quality and consistency across sources.

You will classify, standardise, and group products per business rules, while collaborating with Governance and Business teams to improve reference data structures and processes in a dynamic, multicultural environment.