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Genotoxicity Expert

0-2 years
Not Disclosed
10 April 4, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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Job Title: Genotoxicity Expert

Location: Hyderabad
Job Type: Full-time
Company: Sanofi Consumer Healthcare
Department: Nonclinical Safety / Genotoxicity


About Sanofi Consumer Healthcare

At Sanofi Consumer Healthcare, we create trusted, global brands that empower individuals to manage their own health. As a purpose-driven organization, we aim to integrate sustainability and responsibility into every aspect of our work. We’re seeking innovative and passionate individuals to help us become the best consumer healthcare company for the world.


Key Responsibilities

Genotoxicity Expertise

  • Serve as a genotoxicity subject matter expert for Consumer Healthcare (CHC) drugs and marketed products.

  • Represent the nonclinical genotoxicity function within multi-functional Genotoxicity Project Teams.

  • Conduct scientifically sound nonclinical analysis and categorization of genotoxic potential of CHC products.

Data Collection & Evaluation

  • Search and analyze genotoxicity and carcinogenicity data using internal and external databases.

  • Identify data gaps and verify the validity of studies and results.

  • Gather supporting information on product labeling and safety classifications.

Analysis & Reporting

  • Perform in-depth analysis including weight of evidence assessments based on:

    • Genotoxicity studies

    • Structure-activity relationships

    • Competitor data

    • Clinical and pharmacovigilance (PV) data

    • Labeling information

  • Generate safety assessments for internal documentation and regulatory purposes.

  • Support preparation of MRPTC/SMC presentations.

Study Management

  • Recommend, subcontract, and oversee additional genotoxicity studies as needed.


Why Join Us?

  • 🟢 Inclusive Culture: Diverse, respectful, and inclusive workplace with strong encouragement for women and underrepresented groups.

  • 🕓 Work-Life Balance: Flexible hours and remote work options available.

  • 📈 Career Development: Opportunities for mentorship, training, and career progression.

  • 🤝 Supportive Environment: Collaborative and innovation-driven team culture.


Qualifications & Skills

  • Expertise in genotoxicity, toxicology, pharmacology, or related nonclinical scientific fields.

  • Experience with data analysis and study evaluation in the context of genotoxicity/carcinogenicity.

  • Strong analytical, presentation, and scientific writing skills.

  • Ability to collaborate across functions, including regulatory affairs, pharmacovigilance, and labeling teams.

  • Excellent English communication skills (written and verbal).


Equal Opportunity Statement

At Sanofi, we believe in equal opportunity for everyone, regardless of race, color, religion, gender, sexual orientation, age, nationality, marital status, disability, or gender identity.