GLP In Vitro Research Scientist

As a member of the Pharmacology and Toxicology (In-Vitro) department, you will be responsible for conducting Cytotoxicity and Genotoxicity studies and ensuring their maintenance. Your key responsibilities will include: - Performing validated AMES and Cytotoxicity assays for medical devices according to ISO standards, ensuring accuracy and reliability in toxicological testing methodologies. - Acting as a Study Director for in vitro studies as per the requirements of OECD GLP principle and ISO 17025. - Conducting Invivo Micronucleus assay, Ames assay, and Chromosomal aberration studies. - Authoring comprehensive Standard Operating Procedures (SOPs) for laboratory activities. Your qualifications should include an M.Sc. in life science, with a preference for Biotechnology and Microbiology. Additionally, you should have 1 to 3 years of experience in Pharmacology and Toxicology (In-Vitro) with knowledge of OECD GLP and NABL (ISO/IEC 17025:2017) standards. In terms of skills, you should be proficient in a variety of assays such as AMES, In vitro and In vivo micronucleus test, In vitro and In vivo Chromosome aberration test, Local Lymph Node Assay, Cell Gene Mutation assay, and handling Primary Cell lines. The company offers a range of benefits including a large campus with leave facilities like Casual Leave, Privilege leave, and Sick leave. Additionally, employees can benefit from school/college fees deduction for staff, yearly Annual Health Check Up Report, gym facility, hostel and canteen facility, employee engagement activities, tours, and training opportunities. This is a full-time, permanent position with benefits such as food provided, leave encashment, paid sick time, and paid time off. The work schedule is in the morning shift with the work location being in person.,