VAPI · FULLTIME
Genetic toxicology
MC
Micro Crispr Pvt Ltd
Vapi · onsite · Posted 12d ago
Sourced from
Not disclosed2–5 yrsfulltimeVapi
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Section · 01
About this role
Company Description Micro CRISPR is a new-age biotechnology company dedicated to improving millions of lives through innovative 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 benefits extend far beyond the company, contributing to more resilient and responsible healthcare and biotechnology ecosystems.
Role Description
1. 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*.
2. 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 archival of study records and materials.
Role Description
1. 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*.
2. 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 archival of study records and materials.
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Section · 02
Skills
data integrity requirementsAmes assayGLP PrinciplesOECD Test GuidelinesSOPs