Company Description Micro CRISPR is a current-age biotechnology company dedicated to improving millions of lives through creative scientific solutions. The organization operates with an outlier mindset, encouraging bold ideas and cutting-edge approaches in the life sciences. Core values of sustainability, ethical responsibility, and long-term impact guide its research and development efforts. Micro CRISPR aims to create technologies and practices whose advantages extend far beyond the company, contributing to more resilient and responsible healthcare and biotechnology ecosystems.
Role Description
Qualification & Experience
M.Sc./M.Tech./Ph.D. in Toxicology, Pharmacology, Biotechnology, Microbiology, Biochemistry, Molecular Biology, Life Sciences or related field.
2–5 years of relevant experience in genetic toxicology and/or GLP preclinical studies.
Practical knowledge/experience in Ames assay, Mammalian Micronucleus (MNT) and Chromosomal Aberration (CA) assays.
Knowledge of GLP Principles, OECD Test Guidelines, SOPs and data integrity requirements.




Job Description
Responsible for the overall scientific conduct and GLP compliance of assigned genetic toxicology studies.
Plan, review and oversee Ames, MNT and CA studies in accordance with approved protocols, SOPs and applicable regulatory guidelines.
Supervise study personnel and ensure activities are performed by appropriately trained and qualified personnel.
Review raw data, calculations, controls, deviations and study results for accuracy, integrity and scientific validity.
Evaluate unexpected results, protocol/SOP deviations and determine their potential impact on study integrity.
Ensure appropriate documentation, data integrity and traceability of study records.
Prepare/review and approve GLP study reports, including scientific interpretation and conclusions.
Coordinate with Quality Assurance (QA) during inspections and audits.
Ensure completion, reconciliation and archi

📌 Genetic Toxicology Vapi
🏢 Micro Crispr
📍 Vapi