Sanofi

Biopharma

GRA-CMCLeadSmallMolecule

€54–73k Gentilly, France FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“GRA-CMC Lead Small Molecule at Sanofi. Skills: Regulatory CMC, Small Molecule, Global Regulatory Strategies. Develop global regulatory CMC strategies. Implement global regulatory CMC strategies”

Industry & Context.

Biopharma
Problems you'll solve

Ability to thrive in fast-paced settings across multiple product lines

What They're Looking For.

Must Have

Background in the pharmaceutical industry with solid CMC regulatory proven track record in preparing and managing regulatory filings and responding to Health Authority questions related to submissions, Fluency in English is required

Nice to Have

advanced degree (Masters or PhD) in a science, health-related and/or regulatory field is preferred

What You'll Do.

Develop global regulatory CMC strategies

Implement global regulatory CMC strategies

Act as direct liaison with agencies

Prepare regulatory CMC dossiers

Review regulatory CMC dossiers

Approve regulatory CMC dossiers

Lead cross-functional collaboration

Identify regulatory risks

Manage regulatory risks

Contribute to regulatory science

Contribute to regulatory policy

How You'll Work.

Team & Collaboration

Lead cross-functional collaboration with R&D, Manufacturing & Supply, and Regulatory Operations teams; Experience working in matrix environments; Build positive relationships with agencies; Clearly communicating risk/benefit implications to project teams and stakeholders

Communication Scope

Excellent communication skills (concise, informative, and persuasive)

Full Job Description

**Le contenu du poste est libellé en anglais car il nécessite de nombreuses interactions avec nos filiales à l 'international, l'anglais étant la langue de travail.** _The job posting is in English given the significant interactions required with our global subsidiaries, for which English is the working language_ **Job title** :_Regulatory Affair CMC Lead Small Molecule_ * _Location: Gentilly/ Campus Val de Bièvre_ _About the job_ **As regulatory affair CMC Lead Small Molecule** within **our Global Regulatory Affairs Small Molecule** team, you'll shape and lead global regulatory CMC strategies for both development and marketed products, working at the intersection of science, regulation, and innovation to bring life-changing medicines to patients worldwide. Ready to get started? The Global Regulatory Affairs CMC Organization serves as a critical strategic partner within Sanofi's regulatory framework, bridging the gap between technical development, manufacturing operations, and global regulatory authorities. Our GRA-CMC department ensures compliance while optimizing product approval pathways across the product lifecycle. The GRA-CMC Small Molecule team develops and implements global regulatory strategies for pharmaceutical synthetic products, guided by Sanofi's "Take the Lead" values particularly "Leading Together" and "Being Bold" to bring innovative healthcare solutions to patients worldwide. **About Sanofi:** We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system, and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives. **Main responsibilities:** * Develop and implement global regulatory CMC strategies for both development and marketed small molecule products, executing and adapting them to meet evolving regulatory

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