GLP Invitro Scientist

Job Description: You will be responsible for Cytotoxicity and Genotoxicity studies and their maintenance, including validated AMES and Cytotoxicity assays for medical devices according to ISO standards, ensuring accuracy and reliability in toxicological testing methodologies. You will act as a Study Director for in vitro studies as per the requirements of OECD GLP principle and ISO 17025. Additionally, you should have experience in performing Invivo Micronucleus assay, Ames assay, and Chromosomal aberration. You will be expected to author comprehensive Standard Operating Procedures (SOPs) for laboratory activities. Key Responsibilities: - Conduct Cytotoxicity and Genotoxicity studies - Perform validated AMES and Cytotoxicity assays for medical devices - Act as a Study Director for in vitro studies following OECD GLP and ISO 17025 requirements - Perform Invivo Micronucleus assay, Ames assay, and Chromosomal aberration - Author Standard Operating Procedures (SOPs) for laboratory activities Qualifications Required: - M.Sc. in life-science (Biotechnology and Microbiology Preferred) - 3 to 15 years of experience in Pharmacology and Toxicology (In-Vitro) with OECD GLP, NABL (ISO/IEC 17025:2017) Additional Company Details: The company offers a large campus with leave facilities like Casual Leave, Privilege leave, Sick leave, school/college fees deduction for employee's staff, Yearly Annual Health Check Up Report, Gym facility, Hostel and Canteen facility, Employee engagement activities, tours, training, and more. Work Type: Full-time Benefits: - Flexible schedule - Food provided - Health insurance - Internet reimbursement - Leave encashment - Paid time off - Provident Fund Schedule: - Day shift - Morning shift Performance bonus Work Location: In person,