Hybrid Data Integrity Lead - Pharma Compliance & Training

Sanofi; Geel; Hybrid; EUR 60,000 - 90,000; Full time

Job summary

Sanofi is seeking a Data Integrity Expert in Geel, Belgium, offering hybrid work (3 days on site, 2 days remote). The role focuses on ensuring reliable, compliant data behind medicines, enabling trust in product quality.

You will lead data integrity activities, support CAPA, training, and readiness for inspections. Ideal candidates have 5+ years in data integrity within pharma, strong data analysis skills, and the ability to manage multiple projects across functions.

Qualifications

• 5 years of experience ensuring data integrity regulatory compliance in the pharmaceutical industry.
• Ability to analyze complex data sets and identify patterns, discrepancies and areas for improvement.
• Proven ability to manage multiple projects at the same time, prioritize tasks and deliver on time.

Responsibilities

• Ensure compliance with regulatory requirements and company policies related to data integrity.
• Conduct routine data quality checks and validations to identify and address data integrity issues.
• Develop and deliver training programs on data integrity principles and practices.
• Identify and assess data integrity risks and implement mitigation strategies.
• Ensure proper documentation practices, including data recording, storage and retrieval.
• Investigate data integrity incidents and implement CAPA.
• Oversee continuous improvement initiatives to meet data integrity requirements.
• Ensure inspection readiness and participate in regulatory inspections and audits.
• Generate and review data integrity reports and metrics for management.
• Represent the site locally and participate in COE as requested.

Skills

Data integrity

Regulatory compliance

Data analysis

Project management

Tools

Computerized systems validation

Job description

Sanofi is seeking a Data Integrity Expert in Geel, Belgium, offering hybrid work (3 days on site, 2 days remote). The role focuses on ensuring reliable, compliant data behind medicines, enabling trust in product quality.

You will lead data integrity activities, support CAPA, training, and readiness for inspections. Ideal candidates have 5+ years in data integrity within pharma, strong data analysis skills, and the ability to manage multiple projects across functions.