Histopathology technician

About the role

Echo Neurotechnologies is developing novel Brain Computer Interface (BCI) products for people living with disabilities to restore autonomy and improve quality of life. We are seeking a qualified Senior Histopathology Technician who will perform the essential tasks related to the macroscopic and microscopic preparation, examination, and analysis of tissue samples. The Senior Histopathology Technician will ensure tissue samples are compliantly and adequately prepared for microscopic examination and analysis by the Pathologist. The person in this role will have a keen eye for attention to detail, an understanding of and proficiency in histological techniques, and a commitment to maintaining Good Laboratory Practice (GLP) standards for safety and accuracy. PRIMARY ROLE AND RESPONSIBILITIES Serve as the Senior Histopathology Technician for a variety of biocompatibility, safety, and efficacy studies for medical devices and associated products in accordance with GLP for Nonclinical Laboratory Studies (Title 21, Part 58). Prepare tissue samples for Pathologist macroscopic and microscopic examinations using various techniques such as fixation, embedding, sectioning, staining, mounting, and imaging. Operate and maintain laboratory equipment, including microtomes, tissue processors, staining stations, and cold storage. Work closely with Quality Assurance (QA) to develop and conduct quality control checks to ensure the precision and reliability of laboratory tests and outcomes. Strictly adhere to laboratory protocols and safety procedures to prevent contamination and ensure the accuracy of test results. Manage laboratory supplies by maintaining inventory and working with the Lab Manager and Procurement to order necessary materials, as needed. Work proactively with Study Director to ensure that any protocol changes related to the processing of tissues are approved and documented in accordance with GLP practices. Work collaboratively with department management, CROs, and Quality Assurance (QA) to exceed Sponsor expectations in the conduct of studies. Ensure that unanticipated responses of study data are corrected, accurately recorded, and verified by working directly with the Study Director to maintain documentation of corrective actions in accordance with regulatory guidelines. Review raw data for technical content and regulatory compliance. Contribute to and prepare GLP study reporting for submission to relevant regulatory agencies to support the company's applications for clinical use. Participate in continuing education to stay current with the latest techniques and advancements in histopathology.