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The Head of Site Quality oversees compliance with cGMP, manages quality systems, leads quality teams, and supports regulatory affairs to ensure product safety and quality in biopharma manufacturing.

Lead transition initiatives in Demand Planning, ensuring timely project delivery, governance, and process improvement while overseeing complex transformations.

The Transparency Reporting Specialist ensures compliance with BIMO, manages clinical trial financial data, collaborates with global teams, and identifies process improvement opportunities.

The Project Specialist will develop and implement communication plans, create tailored content for audiences, manage internal communications, and collaborate with stakeholders to enhance employee engagement.

The Senior Analyst will manage data collection and reporting for transparency obligations in Asia & Oceania, ensuring compliance and data integrity across systems like OneCRM and SAP.

The Master Data Manager will ensure quality master data management, lead a team, propose improvements, and maintain effective data governance at Sanofi.

The Master Data Steward ensures master data quality, supports improvement initiatives, maintains user support, and monitors operational responsibilities related to master data management.

The Senior Master Data Steward ensures master data quality and availability, supports improvement activities, manages data maintenance, and educates the master data community while adhering to data governance frameworks.

The A2R Digital Close Administrator provides technical support for the Digital Close processes using the Blackline tool, manages user requests, coordinates testing, and maintains system operations throughout the implementation and run phases.

Carry out microbiological testing and ensure compliance with GLP/cGMP. Responsible for documentation, laboratory efficiency, and audits. Handle electronic data and maintain laboratory safety.