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Assistant Director - Genetic Toxicology

15-22+ years
Not Disclosed
10 Dec. 5, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Assistant Director – Genetic Toxicology

Location: Bengaluru, Karnataka, India
Employment Type: Full-Time


Company Overview

Eurofins Advinus is a premier preclinical and early development Contract Research Organization (CRO) specializing in drug discovery, preclinical development, and regulatory toxicology services. Our expertise spans discovery services, DMPK, analytical R&D, API CDMO, and GLP-compliant toxicology studies.

With over 30 years of GLP compliance and certification, Eurofins Advinus supports diverse industries including biotechnology, pharmaceuticals, biologics, agrochemicals, nutraceuticals, and cosmetics. We are the only CRO in India to have developed data supporting over 90 end-to-end IND-enabling packages submitted to global regulators, including USFDA, EMA, MHRA, Health Canada, and others.


Role Overview

We are seeking a highly experienced Assistant Director – Genetic Toxicology to lead and manage our genetic toxicology operations. The ideal candidate will have extensive expertise in genotoxicology, proven leadership in managing laboratory teams, and a strong track record in regulatory and non-regulatory study execution. This role requires strategic oversight of study planning, execution, reporting, compliance, and client engagement to ensure the highest standards of scientific excellence and regulatory adherence.


Key Responsibilities

  • Provide scientific leadership in genotoxicology, overseeing the design, execution, and interpretation of studies in compliance with FDA, EMA, ICH, and OECD guidelines.

  • Manage studies including Bacterial Reverse Mutation (Ames Test), Bone Marrow Micronucleus Test, Chromosome Aberration Test, and In Vitro Micronucleus Test.

  • Prepare, review, and approve study plans, protocols, amendments, study reports, and SOPs.

  • Lead, mentor, and manage a team of genetic toxicologists and study directors to ensure consistent performance and adherence to GLP standards.

  • Oversee laboratory operations, including equipment validation, calibration, procurement of reagents, and maintenance.

  • Collaborate with HOS/HOD in budgeting, planning, resource allocation, and development of new platforms.

  • Maintain robust client communication, ensuring timely delivery of services and fostering repeat business opportunities.

  • Support business development and marketing initiatives, contributing to new business generation and operational growth.

  • Participate in GLP/NABL inspections, quality audits, and ensure compliance with regulatory guidelines.

  • Standardize and implement new in vitro test procedures to enhance laboratory capabilities.


Qualifications and Experience Required

  • M.V.Sc / M.Sc in Microbiology with 20–22+ years of relevant industry experience or

  • PhD in Microbiology with 15+ years of relevant industry experience.

  • Strong understanding of agrochemical and pharmaceutical R&D processes.

  • Demonstrated expertise in regulatory toxicology and genotoxicology study design and execution.

  • Proven experience in managing internal teams and external collaborations.

  • Ability to adapt to rapidly changing scientific and regulatory environments.

  • Strong problem-solving, analytical, and decision-making skills.


Behavioral Competencies

  • Excellent oral and written communication skills.

  • Ability to work efficiently in a dynamic and fast-paced environment.

  • Strong time management skills to handle multiple projects simultaneously.

  • Highly motivated with a commitment to continuous learning and professional growth.

  • Effective training, presentation, and team mentoring capabilities.

  • Innovative mindset with the ability to conceptualize, implement, and optimize new ideas.


Why Eurofins Advinus

  • Be part of a globally recognized CRO with international regulatory exposure.

  • Lead a high-performing team in a state-of-the-art, GLP-certified laboratory.

  • Competitive compensation and benefits aligned with industry standards.

  • Opportunity to contribute to global drug development projects and innovative genotoxicology research.


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