Sanofi

Biopharma

AnalyticalDevelopmentSeniorScientist

€48–64k Sisteron, France FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Analytical Development Senior Scientist at Sanofi. Skills: Analytical development, Method validation, Project management, GMP. Develop analytical methods. Validate analytical methods”

Industry & Context.

Biopharma
Problems you'll solve

Analytical investigations

What They're Looking For.

Must Have

Master degree or analytical chemistry Engineer with 4 years of experience, PhD with 2 years of experience, Expertise in pharmaceutical analytical development, Expertise in project management, Good knowledge in chromatography (LC-UV and GC-FID), Good knowledge in physico-chemical analytical techniques, Good knowledge in project management, Knowledge in GMP rules, Knowledge of galenics, Knowledge of organic chemistry, English good level (writing, speaking), French good level (writing, speaking)

Nice to Have

AI knowledge, Digital tools knowledge, Modeling knowledge, Automation knowledge

What You'll Do.

Develop analytical methods

Validate analytical methods

Write method documentation

Ensure timely completion of internal work

Ensure timely completion of external work

Ensure compliance with GMP standards

Supervise analytical studies

Write analytical sections for dossiers

Represent unit in project teams

Make scientific presentations

Manage laboratory equipment

Manage laboratory budget

Provide analytical support for chemists

Provide analytical support for pilot plant operations

Lead analytical investigations

Lead stability studies

Monitor emerging trends in analytics

Monitor emerging trends in technology

Monitor emerging trends in automation

Monitor emerging trends in AI

Drive innovation initiatives

Act as technical expert

Provide training to colleagues

Provide support to colleagues

How You'll Work.

Team & Collaboration

Project teams; Scientific presentations; Internal partners; External partners; Diverse teams

Communication Scope

Scientific presentations; Interaction with partners

Process & Methodology

Project management

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._ _This job offer is accessible to all, regardless of gender._ **Job titl****e:**_**** Analytical Development Senior Scientist_ * _Location: Sisteron_ # _About the job_ __ As **Analytical Development Senior Scientist** within our Analytical Development team, you'll develop analytical methods for synthetic small molecules and manage CMC projects as part of our synthetic platform. Ready to get started? Our analytical group is part of the synthetic platform within Global CMC Development, striving to become an industry leader in the development of transformative medicines. You'll play a key role in developing and validating analytical methods for pharmaceutical small molecules while managing projects as an analytical representative or Team Lead, ensuring compliance with GMP standards and regulatory requirements. **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 validate analytical methods (LC, GC, potentiometry, water content) for pharmaceutical small molecules, including writing protocols, reports, and method documentation * Manage CMC projects as analytical representative or Analytical Team Lead, defining budgets and ensuring timely completion of internal and external work * Ensure compliance with GMP standards for required studies and supervise analytical studies according to scientific and regulatory requirements * Write analytical sections for clinical and submission dossiers and represent your unit in project teams and scientific pres

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