Lab Supervisor 004

Monitor test analysis and specimen examinations to ensure that acceptable levels of analytic performance are maintained. Manage and perform toxicology screening and confirmation by following various chemical procedures with patient specimens using analytical equipment. Perform quality control procedures according to established protocol. Manage and perform pathogen detection in laboratory. Assist with and supervise various research projects. Perform remedial actions and record all quality control failures and corrective actions according to established protocol. Verify all assays are in control before releasing patient results. Perform calibration of instruments as necessary and ensure calibration period is adequate to cover testing. Calculate results according to established protocol. Follow established protocols for analysis, quality, and ancillary procedures. Judge acceptability of specimens and rejects/requests new specimens as indicated. Interrupt testing to perform STAT procedures when necessary. Process requests and investigates complaints through to resolution from physicians, staff, and patients. Check lot numbers when restocking instruments or starting new kits. Participate in internal and external continuing education when required. Conduct laboratory in-services. Participate in method validation for new procedures and/or equipment. Participate in developing/writing new standard operating procedures (SOP's) and revising old ones. Adhere to laboratory and hospital safety practices, including but not limited to OSHA bloodborne pathogens, HIPAA, and hazardous chemicals training and monitoring. Answer inquiries regarding test results, methodologies, test specificity, test sensitivity, and factors that can influence test results. Develop new and revises existing policies and procedures, as needed. Rotate stock and maintains adequate inventory, notifies appropriate personnel when stock is low. Participate in Proficiency Testing, if involved in routine patient specimen testing.

Position requires a Master's in Pharmacology, Toxicology or related field and twelve (12) months of experience. One (1) year experience must have included: CLIA/COLA/OSHA/SAMHSA laboratory regulations, supervising labs and lab staff, supervising research projects, mentoring and training lab staff.

To apply, please send resume and cover letter referencing ref. # 474.004 to: [email protected] or by U.S. Postal Mail to: ADVANCED HEALTH INFORMATICS, LLC, 8628 Industrial Parkway, Suite E, Plain City, Ohio 43064.