GLR is continuously looking for excellent candidates with a great attitude from various fields - medical, veterinary, toxicology, biological sciences, and quality.
GLR Laboratories Pvt Ltd, specializing in medical device biocompatibility testing (in vitro and in vivo), is looking for two (one junior and one mid-level) toxicological risk assessment specialists to join our regulatory toxicology group at our Chennai office. Candidates preferably should be board certified in toxicology. Candidates should have a background in pharmacology/toxicology and human health risk assessment; and be proficient technical writers able to work independently in a fast-paced contract research environment. Every project is unique and risk assessments must comply with FDA, EU-MDR and ISO regulations. Toxicological risk assessments involve evaluating chemical characterization data on medical devices, deriving exposure estimates for clinical use scenarios, conducting literature research on chemical-specific toxicity, and assessing the margin of safety from exposure to individual chemicals. Other consulting roles include evaluation of biological (in vitro/in vivo) testing results to establish the safety of medical devices and assisting in study design and recommending further testing where needed. Interested candidates please send your CV and cover letter detailing your experience in human risk assessment to email@example.com.
Managing and monitoring the allocation of Toxicology studies to Study Directors in the team Providing leadership, management, training and development to the team Ensuring that Study Directors in the team progress high quality reporting so that reports are submitted to QA on time and issued to clients within allocated time frames Communicating effectively with the team to ensure that everybody is aware of the expectations placed upon them by the business, and how the business is performing Providing monthly updates to the Director of Toxicology on team workloads, study starts and reporting status.