Assistant Director - Bengaluru / Bangalore - confidential

    confidential
    confidential Bengaluru / Bangalore

    6 days ago

    Full time
    Description
    • 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 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.
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