Glp in Vitro Research Scientist
5 days ago
**Department: Pharmacology and Toxicology (In-Vitro)**
**Qualification**:M.Sc. in life-science (Biotechnology and Microbiology Preferred).
**Experience**:
- 1 to 3 years of experience in Pharmacology and Toxicology (In-Vitro) with OECD GLP, NABL (ISO/IEC 17025:2017).
**Job description**:
- Responsible for Cytotoxicity and Genotoxicity studies and their maintenance.
- Validated AMES and Cytotoxicity assays for medical devices according to ISO standards, ensuring accuracy and reliability in toxicological testing methodologies
- To act as a Study Director for in vitro studies as per the requirements of OECD GLP
- principle and ISO 17025.
- Should have performed Invivo Micronucleus assay, Ames assay & Chromosomal aberration.
- Authored comprehensive Standard Operating Procedures (SOPs) for laboratory activities
**Skills**:
Assays: AMES- bacterial reverse mutation assay, In vitro and In vivo micronucleus test and biochemistry parameters In vitro and In vivo Chromosome aberration test, Local Lymph Node Assay, Cell Gene Mutation assay Primary Cell lines handled.
Work Location: In person
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