Project Toxicologist

Sanofi

Marcy-l'Étoile

Sur place

EUR 60 000 - 80 000

Plein temps

14 jours+

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Avantages offerts par ce poste

Quality health insurance
31 days of paid leave
Remote working opportunities
Profit-sharing and incentive schemes

Résumé du poste

Sanofi in Marcy-l'Étoile seeks a Project Toxicologist to provide safety strategy and conduct assessments of vaccines and therapeutic modalities. You will manage toxicology studies and compile safety data for regulatory documentation.

The ideal candidate will possess a toxicology-certified background, with demonstrated experience in vaccine development and regulatory knowledge. Enjoy a rich benefits package including paid leave, healthcare, and a dynamic work environment.

Qualifications

  • Demonstrated experience in vaccine toxicology or biopharmaceuticals.
  • Ability to manage workload and communicate effectively among project teams.
  • Experience as study director in toxicology.

Responsabilités

  • Conduct toxicological safety assessments on new components.
  • Evaluate study outcomes and provide risk assessments.
  • Manage GLP/non-GLP toxicity studies for timely delivery.

Connaissances

Toxicology
Communication skills
Team spirit
Regulatory standards knowledge

Formation

PhD in Toxicology or related field

Description du poste

Job Title

Project Toxicologist

Location
  • Marcy-l'Etoile – France
Overview

As Project Toxicologist within NCS & Predictive Sciences, you will provide safety strategy, supervise toxicology experiments, and conduct safety assessments of vaccines, adjuvants, and monoclonal antibodies across all R&D stages and Life Cycle Management products. You will coordinate with other disciplines to evaluate the impact of study outcomes on product development, provide integrated risk assessments to project teams, and compile safety data into regulatory documentation. Your expertise will directly support the development of innovative prophylactic or therapeutic modalities that improve patient safety.

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.

Key Responsibilities
  • Provide safety strategy and conduct toxicology evaluations and risk assessments in support of new vaccine projects.
  • Conduct toxicological safety assessments on new components, excipients, or process residues.
  • Evaluate study outcomes and data, provide assessment on the adversity of findings and potential impact on human health and project progression.
  • Manage and monitor the conduct of GLP/non‑GLP toxicity studies to ensure timely delivery, compliance, and quality of reporting.
  • Compile safety data into necessary internal, clinical, and regulatory documentation (IB, IND, IMPD, CTA, CTD, RMP, PBRER, Labelling, Pediatric plans) and provide answers to regulatory body questions.
  • Provide and communicate integrated risk assessments to project teams and partners, and contribute to meetings with Health Authorities.
  • Support NCS to ensure continuous improvement on core competencies, processes, and work practices.
  • Promote operational excellence through development and execution of appropriate processes and engagement with New Approach Methodologies (NAMs).
What We Offer
  • A fixed salary over 12 months, complemented by an individual variable compensation, as well as profit‑sharing & incentive schemes based on Sanofi Group results.
  • 31 days of paid leave plus RTT days depending on your status, remote working up to 2 days per week, quality health insurance, public transport coverage up to 80%, maternity leave (18 weeks) and parental welcome leave (14 weeks), Savings & Retirement Plans with employer contributions, employee benefits (CSE), internal and international mobility opportunities, a personalized training offering, and many more benefits.
Experience

Demonstrated experience in vaccine toxicology and/or biopharmaceuticals with experience as study director in toxicology and project representative. Good understanding of vaccine and biopharmaceutical development with experience in R&D environment, pharmaceutical industry, and animal models.

Technical and Soft Skills
  • Broad expertise in human and animal pathophysiology, pharmacology, and toxicology.
  • Excellent communication skills with ability to manage workload, urgencies, and priority queries while maintaining high‑level communication between all project actors.
  • Strong team spirit and ethical responsibility towards laboratory animals and clinical trial volunteers.
  • Knowledge of regulatory standards and NAMs.
Education

Toxicology‑certified background (PhD, Pharmacist, DVM, MD or certification in toxicology).

Languages

Fluent English and French (written and oral).

Why Choose Us
  • Work at the forefront of drug discovery, harnessing cutting‑edge AI, data, and digital platforms to push the boundaries of science.
  • Help improve the lives of millions of people globally by making drug development quicker and more effective.
  • Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs.
  • Accelerate your professional development with structured career paths designed for both scientific and leadership advancement. Grow in ways you never imagined through bold moves that stretch your potential, cross moves into other business areas, and short‑term gigs that build your scientific expertise.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

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.

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