Full-time
Genetic Toxicology Study Director
Posted by Micro Crispr Pvt. Ltd. • Not Specified, Gujarat, India
About the Role
- To acquire knowledge and be knowledgeable in those parts of the Principles of GLP which are applicable to involvement in the study.
- Should have the awareness for the basic principles of OECD GLP.
- Design, plan, and monitor in vivo and in vitro genetic toxicology studies (AMES, Cytotoxicity, Micronucleus test, Comet Assay, Chromosomal test, HPRT, MLA studies, etc.,) in accordance with regulatory guidlines(e.g.,OECD, ICH, EPA, ISO).
- To scientifically conduct the non clinical safety studies in compliance with the Principles of GLP, regulatory guidelines and animal welfare guidelines like CPCSEA.
- Record and maintain study data in accordance with ALCOA+ and data integrity standards.
- Handle cell cultures, bacterial strains, and appropriate laboratory models as per the assay requirements.
- To take part and monitor the studies related activities like study designing, study plan writing, experimental procedures, data recording and anal...
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