Oversee and maintain the Chemistry department workflow and ensure the department follows safety and quality assurance procedures. This includes reagent supply usage, maintenance flow, instrument training and training documents.
Requirements
Bachelor’s degree in science
Master’s Degree
National certification by the American Society of Clinical Pathology (ASCP) as applicable, or as a Medical Technologist (MT) preferred.
Maintains appropriate continuing education and to increase basic
Must have proven track record in physician, employee and client relationships and operational performances.
Experience with the validation protocol for LCMS testing
Responsibilities
Support PathGroup’s mission, vision, goals, and management
Provide scientific oversight of timely selection, development and validation of assays in LC/MS-MS area. Assists in strategic development of the laboratory services
Ensure compliance with laboratory regulatory
Support all processes involved with Quality Management which include solving problems, developing procedures, and trending and reporting data.
Implement and maintain effective departmental Quality Assurance and Quality Improvement programs and monitors.
Organize QC lot changes tracking expirations and shipment process per CAP
Reviewing reports from laboratory equipment to ensure everything is operating in an efficient manner.
Maintain calibration programs for testing equipment that affect quality
Responsible for the continuity between all areas of the department that includes departmental procedures, validations, and maintaining inspection readiness.
Ensure effective employee relations by sustaining an ethical, non-discriminatory and safe work environment and establishing effective communication lines and methods.
Assist in establishing and executing departmental long and short-term
Become familiar with and abide by the Corporate Compliance Program and all Corporate policies, including the Privacy and Security policies
Follow guidelines and SOPs for reviewing and releasing
Support training programs by writing SOP’s and working with Medical Technologist to ensure everyone is knowledgeable on instrumentation and work flow.
Review and monitoring of LCMS consumables and comparative inventory.