Company: Sanofi

Location: Toronto, ON

Expected salary:

Job date: Tue, 03 Jun 2025 22:16:23 GMT

Job description: 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 jobLooking 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 youExperience:

• 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).

Why choose us?iMove is a unique program tailored for European youth interested in challenging themselves with meaningful assignments across the globe. At Sanofi we have a strong ambition to invest in young talents who will drive the success of Sanofi tomorrow.Sanofi’s Work Abroad Program, iMove, offers jobs-assignments with actual responsibilities and a perspective to grow. We provide those opportunities in various functions such as: marketing, finance, regulatory, supply chain, clinical trials, production, etc. and in more than 40 countries. Sanofi unites people who are passionate about solving healthcare needs across the world. Joining our iMove Work Abroad Program is a unique opportunity to make a difference through your work.#LI-EURPursue progress, discover extraordinaryBetter is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our and check out our Diversity Equity and Inclusion actions at !

Job Summary: Data Governance and Quality Analyst – VIE Contract

Location: Toronto, Canada
Start Date: October 1, 2025
Program: iMove (Sanofi VIE Program) for EU citizens aged 18-28. Only applications in English will be considered.

Job Overview:
Join Sanofi’s Regulatory Affairs team as a Data Governance and Quality Analyst. Gain experience in data governance, quality assurance, and data analysis, helping improve healthcare outcomes globally.

Responsibilities:

• Support data governance and compliance in the Regulatory Information Management (RIM) system.
• Collaborate with data stewards and various functional teams on data changes and impact analysis.
• Assist in data remediation tasks and manage the Quality Dashboard.
• Engage with multi-functional and multicultural teams globally.

Requirements:

• 1-3 years of experience in an analyst role, preferably in Pharmaceutical Regulatory Affairs or Quality Operations.
• Proficient in Microsoft Office; strong analytical and communication skills in English.
• Ability to work collaboratively, adapt to change, and manage sensitive data.

Education:
Bachelor’s or Master’s in Regulatory Affairs, Sciences, or related fields.

Why Sanofi?
The iMove program offers meaningful responsibilities and growth opportunities across various functions in over 40 countries. Sanofi values diverse backgrounds and aims to empower young talents for future success.

Equal Opportunity:
Sanofi is committed to diversity and inclusion in the workplace.