Data Governance and Quality Analyst - VIE Contract

Data Governance and Quality Analyst - VIE Contract

• Location: Canada, Toronto
• Target start date: 01/10/2025

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address.

About the job

Looking to launch your career at the cutting edge of healthcare? Join Sanofi for a chance to develop with mentoring and guidance from inspirational leaders while helping to make an impact on the lives of countless people worldwide. As Data Governance and Quality Analyst VIE in our Regulatory Affairs team you will have the opportunity to develop skills and experience across various Data teams here at Sanofi.

We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.

Main responsibilities:

• This role is within the Reg Data Quality and Quality group under the Global Submission Management & Data Operations (GSMDO) in Global Regulatory Operations (GRO).
• Support Data Governance (DG), Data Stewards on various requests and projects to maintain compliant data formats and objects in the global Regulatory Information Management (RIM) system. This is done in partnership with Global Regulatory Affairs (GRA) corporate plus affiliates, contributing Data Owner functions as well as with Digital and vendors.
• Work with various functional groups on future data changes, standards and impact analysis especially related to tool functionality and system integrations. 
• Support the Data Remediation team with request analysis, retrieving data and performing tasks such a loader preparation and execution within Vault System.
• Support the Quality Team in the maintenance of Quality Dashboard and performing Data Analysis of various sets of data or reports.
• Supports business data models, data flows and data lineage mapping.
• Support the Data Operational Experience (DOX) team requests as needed, to help users with tasks within the system, help with communication and analyzing data and issue to determine a solution.
• Works transversally with RIM users from all GRA functions, globally and regionally.
• Supports the teams’ end to end project process.

About you

Experience:

• 1-3 years' experience in an analyst role/function is preferred.
• Background in Pharmaceutical Regulatory Affairs and Quality Operations is preferred.
• Experience with Pharmaceutical Regulatory Data and Standards and data analysis is an asset.

Soft and Technical skills:

• Experienced in Microsoft Office and Windows (Outlook, Word, Excel, PowerPoint).
• Ability to embrace new activities.
• Ability to work with multifunctional and multicultural teams.
• Collaborative team player with orientation towards building and maintaining effective relationships, strong culture awareness.
• Ability to communicate in English (verbally and written) effectively and efficiently across varying functions and levels of management.
• Ability to operate with agility in a dynamic global environment.
• Ability to propose solutions and proactivity.
• Ability to maintain discretion and confidentiality about sensitive data.
• Strive to meet short deadlines and shifting priorities.
• Demonstrated continuous improvement mindset.

Education:

• Bachelor’s or Master’s degree in Regulatory Affairs, Sciences or related field.

Languages:

• Fluent English (written and verbal).