Assistant Director - Genetic toxicology

• Provide in-depth scientific leadership in Genotoxicology with extensive experience in designing, executing, and interpreting genetic toxicology studies.
• Conduct and oversee regulatory (FDA, EMA, ICH, OECD) and non-regulatory studies, ensuring adherence to global guidelines and standards.
• Lead studies including but not limited to: Bacterial Reverse Mutation Test (Ames Test), Bone Marrow Micronucleus Test, Chromosome Aberration Test, and In Vitro Micronucleus Test.
• Responsible for planning, execution, performance, documentation, reporting, and archiving of genotoxicology studies.
• Prepare study plans, protocols, amendments, and reports; create and review SOPs in alignment with GLP and regulatory requirements.
• Manage and mentor a team of genetic toxicologists, providing guidance to ensure high performance and goal alignment with departmental and organizational objectives.
• Supervise study directors across multiple projects to ensure consistency, compliance, and timely delivery.
• Train and onboard new team members to meet GLP standards and expected technical proficiencies.
• Develop monthly forecasts and performance reports; manage resources efficiently to meet scientific and operational goals.
• Maintain strong client relationships, ensuring timely communication and delivery of high-quality services to promote repeat business.
• Oversee laboratory maintenance, equipment validation and calibration, and procurement of supplies to support uninterrupted study execution.
• Participate in GLP/NABL inspections and activities, ensuring compliance with QA checklists and regulatory standards.
• Collaborate with HOD/HOS for budgeting, planning, costing, and expansion of service offerings and capabilities.
• Support business development and marketing efforts by engaging with clients, providing scientific input, and generating leads.
• Standardize and implement new in vitro genetic toxicology procedures and platforms.

Qualifications / Experience:

• PhD in Microbiology with minimum 15+ years of relevant industry experience, or
• Master's in Microbiology (M.V.Sc / M.Sc) with minimum 20-22+ years of relevant industry experience.
• Strong understanding of agrochemical and pharmaceutical R&D processes.
• Proven ability to manage internal and external scientific collaborations.
• Experienced in handling changing regulatory and scientific landscapes.
• Strong leadership and people development skills.