Biopharma Histology Technologist

PathAI•Memphis, TN

2d•$23 - $30•Onsite

About The Position

PathAI is on a mission to improve patient outcomes with AI-powered pathology. We are transforming traditional pathology methods into powerful, new technologies. These innovations in pathology can help accelerate drug development, improve confidence in the accuracy of diagnosis, and get life-saving therapies to patients more quickly. At PathAI, you'll work with a diverse and talented team of people, who are dedicated to solving complex problems and making a huge impact. You will participate in clinical trials of novel drugs designed to improve the quality of life for people suffering with various diseases. We are searching for a talented Histotechnician for our Biopharma Laboratory located in Memphis, TN. This person will be responsible for performing histological processing and staining of a full range of biopsy tissue and report to the Head of the Biopharma labs. The ideal candidate is someone who has a passion for healthcare with a strong attention to detail and is ready to apply their skill set in a fast-paced and growing company helping shape AI-powered pathology.

Requirements

Experience in a pathology laboratory.
Familiarity with lab quality systems (GCP/GCLP, CAP/CLIA, ISO) and best practices for clinical labs.
Education: Eligible to perform High Complexity testing as per CLIA.
Detail oriented, excellent record keeping.
Growth mindset, willingness to learn new methodologies and innovate on quality process development.
Excellent communication skills, ability to develop presentations and interact with stakeholders as needed.

Nice To Haves

Certification/License: Histotechnician (HT) ASCP certification is preferred.
Familiarity with test process qualification/validation and proficiency testing is a preferred.

Responsibilities

Responsible for performing gross pathology, tissue processing, embedding, sectioning, staining utilizing standard protocols and instrumentation for established assays.
Help accession samples and relevant information into the appropriate Laboratory Information Management System (LIMS).
Responsible for evaluating data quality and flagging any data deviation.
Follow relevant lab quality systems (GCP, CAP/CLIA) for documenting process deviations and quality control measures and remediation.
Responsible for developing and/ or processing biological samples as part of new method development.
Involved in the validation of new methods, method development, troubleshooting of assays and development of SOPs.
Assist with lab maintenance activities.
Be rigorous and prompt in process documentation and reporting, communication.

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