What are the responsibilities and job description for the 2nd Shift Clinical Molecular Technologist position at Belay Diagnostics?
PURPOSE :
Must be authorized to work in the United States. With minimal oversight from the Manager / Supervisor of the Laboratory, the Molecular Technologist will be responsible for processing both clinical and research samples using cutting-edge technologies for nucleic acid analysis, including but not limited to next-generation sequencing, Sanger sequencing, qPCR and associated sample preparation technologies. These activities are performed under CLIA / CAP regulations and will directly impact human health and thus must meet the highest possible standards for quality and integrity. Technologist roles are distinguishable primarily by level of experience, supervision required, proficiency in problem solving, certification and wider range of training.
Must have experience performing NGS assays in a high complexity clinical laboratory.
KEY RESPONSIBILITIES :
This role is responsible for the efficient and quality execution of sample accessioning, processing and data generation for the Laboratory. This includes working with the manager to maintain all documentation required for operation under CLIA / CAP certification, including review and writing of SOPs as necessary and use of sample tracking systems in accordance with standard operating procedures.
- Timely completion of training assigned by management or laboratory director to meet the needs of laboratory operations
- Ensure sample accessioning is performed in an accurate manner to enable effective testing of samples downstream as ordered.
- Work with pathologist to evaluated neoplastic content of sample as needed
- Sample processing including nucleic acid purification and preparation for sequencing and PCR is performed per established processes
- Accurate and timely maintenance of operational metrics
- Maintains and updates associated process documentation, participates in continuous process improvements and ongoing training
- Performs quality control of samples processed and data generated prior to sending to next steps.
- Maintenance of auxiliary and capital equipment and instrumentation
This role is also responsible for the development and validation of new methodologies, including establishing novel workflows, evaluating new instrumentation and protocols as deemed necessary by the clinical laboratory manager and / or director
MINIMUM QUALIFICATIONS :
