Job Number:
HC-03697
Date Posted:
March 9, 2026
Position Title:
Manager Regulatory Affairs
Party:
N/A
Office Code:
Office/Company:
Sanofi
Reports To:
Location:
Cambridge, MA | Morristown, NJ
Contact:
Salary:
Primary Role
Secondary Role:
Job Type:
Full Time
Description:
Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.- Identifies product specific or therapeutic area A&P issues and works with other teams to propose and implement solutions. - Identifies different strategies for addressing issues; advises of risk/benefit of each and assists clients with making sound business decisions with the understanding of the potential risk/benefits with respect to intervening regulatory matters.Bachelor’s degree in Life Sciences from an accredited four-year college or university.
Responsibilities:
• Identifies product specific or therapeutic area A&P issues and works with other teams to propose and implement solutions.
• Identifies different strategies for addressing issues; advises of risk/benefit of each and assists clients with making sound business decisions with the understanding of the potential risk/benefits with respect to intervening regulatory matters.
• Oversees and bears responsibility for the successful implementation of regulatory strategic objectives and projects with minimal supervision.
• Active participant and Regulatory representative on brand teams and Review Committees (RC) for commercial and medical materials, respectively.
• Provides guidance and feedback to internal Sanofi constituencies (commercial groups, R&D) to maximize the competitive impact of product development as well as ultimate promotion, advertising, and reimbursement.
• Contribute A&P expertise to the development of optimal labeling on new and supplemental new drug applications.
Qualifications:
• Bachelor’s degree in Life Sciences from an accredited four-year college or university.
• 1-3 Years experience in the following areas:
• Experience within pharmaceutical or medical device Regulatory Affairs.
• Successful track record with ideally 1-3 years relevant regulatory experience.
• Dealt effectively with cross-functional groups, which may include Medical, Legal, Marketing etc.
Instructions:
Email <ddress>
Other:
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce.
