Regional Qualification Specialist – Data & Validation Lead

Sanofi

Bogotá

Híbrido

COP 90.000.000 - 144.000.000

Jornada completa

Hace 9 días
Generador de candidaturas

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Ventajas ofrecidas por este puesto de trabajo

Flexible remote work
Private medical care
Life insurance
Gender-neutral parental leave

Descripción de la vacante

Sanofi is seeking a Regional Qualification Specialist in Bogotá to link R&D and Manufacturing, ensuring qualification of equipment, utilities, and facilities. The role supports data analysis, reporting, and validation documentation across the portfolio and future launches.

The candidate should have a background in pharma/biotech validation, strong English, and be proficient with quality systems and data analytics, with flexible remote options up to 50%.

Formación

  • Professional experience collecting, qualifying and re-qualifying data
  • Experience with data sets, protocols and reports
  • Ability to generate graphs/tables for qualification data
  • Ability to ensure data integrity across deliverables
  • Knowledge of validation/qualification processes and documentation standards

Responsabilidades

  • Collect and compile raw data for qualification/re-qualification reports.
  • Create graphs/tables from data using appropriate tools.
  • Prepare data sets to support qualification analyses.
  • Analyze data per protocol and verify against acceptance criteria.
  • Assist in writing reports using approved templates.
  • Maintain data quality and integrity across deliverables.
  • Keep data updated in designated systems.

Conocimientos

Quality systems
Data analysis
Problem solving
Attention to detail
Cross-functional collaboration
Documentation

Educación

Bachelor's degree in pharmacy, engineering, chemistry, biology, or related field

Herramientas

Veeva
Kneat
Microsoft Office

Descripción del empleo

Sanofi is seeking a Regional Qualification Specialist in Bogotá to link R&D and Manufacturing, ensuring qualification of equipment, utilities, and facilities. The role supports data analysis, reporting, and validation documentation across the portfolio and future launches.

The candidate should have a background in pharma/biotech validation, strong English, and be proficient with quality systems and data analytics, with flexible remote options up to 50%.

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