Manager Operations Regional Laboratory (Durational w/Benefits)
Kaiser Permanente
Description: Job Summary:
Directs and controls the day-to-day operations for their specific area of responsibility, which includes all personnel activities, technical oversight, general work flow, and budget. Ensures compliance with federal, state, and local requirements.
Essential Responsibilities:
Directs and controls the day to day operations for one or more of the following areas: chemistry, hematology/coagulation, urinalysis/bacti, blood bank, point of care, general lab and/or quality control assurance.
Recruits, hires, trains, and ensures competency of staff.
Motivates and encourages professional and personnel growth.
Controls costs by monitoring personnel utilization, material usage rates, analyzing fluctuations in types and volumes of tests, and implementing corrective action.
Directs and implements effective risk control processes.
Supports, consults, and participates with facility and regional QA programs to ensure internal and external regulatory compliance.
Assists in developing and monitoring section specific QA/Risk Management program.
Assists in monitoring quality assurance for laboratory information systems.
Researches/resolves client problems/issues.
Oversees and coordinates operational aspects within various subsections of the clinical laboratory.
Participates in department, inter-department and inter-facility projects which help the laboratory achieve its goals of providing quality service and client support in a cost effective manner.
Develops equipment and system needs analysis as appropriate.
Coordinates the integration of secondary laboratory information systems with RILIS.
Interfaces with lab manager to implement and monitor an internal and external complaint/incident program.
Coordinates and implements a safety program to include fire, hazardous wastes, infectious wastes, electrical, chemical.
Coordinates a program of continuing education in the area of safety.
Coordinates internal resources and monitors milestones to achieve service expectations. Basic Qualifications:
Experience
Minimum three (3) years of experience in a high-volume clinical laboratory.
Education
Bachelors degree in clinical laboratory science or related field required, OR four (4) years of experience in a directly related field.
High School Diploma or General Education Development (GED) required.
License, Certification, Registration
Clinical Laboratory Scientist License (California)
Additional Requirements:
Knowledge of CLIA, Title 22, CAP, JCAHO, NCQA, AABB, local, state, federal regulations.
Must be able to work in a Labor/Management Partnership environment.
Preferred Qualifications:
Previous experience in a supervisory/managerial position preferred.
Masters degree preferred.
Directs and controls the day-to-day operations for their specific area of responsibility, which includes all personnel activities, technical oversight, general work flow, and budget. Ensures compliance with federal, state, and local requirements.
Essential Responsibilities:
Directs and controls the day to day operations for one or more of the following areas: chemistry, hematology/coagulation, urinalysis/bacti, blood bank, point of care, general lab and/or quality control assurance.
Recruits, hires, trains, and ensures competency of staff.
Motivates and encourages professional and personnel growth.
Controls costs by monitoring personnel utilization, material usage rates, analyzing fluctuations in types and volumes of tests, and implementing corrective action.
Directs and implements effective risk control processes.
Supports, consults, and participates with facility and regional QA programs to ensure internal and external regulatory compliance.
Assists in developing and monitoring section specific QA/Risk Management program.
Assists in monitoring quality assurance for laboratory information systems.
Researches/resolves client problems/issues.
Oversees and coordinates operational aspects within various subsections of the clinical laboratory.
Participates in department, inter-department and inter-facility projects which help the laboratory achieve its goals of providing quality service and client support in a cost effective manner.
Develops equipment and system needs analysis as appropriate.
Coordinates the integration of secondary laboratory information systems with RILIS.
Interfaces with lab manager to implement and monitor an internal and external complaint/incident program.
Coordinates and implements a safety program to include fire, hazardous wastes, infectious wastes, electrical, chemical.
Coordinates a program of continuing education in the area of safety.
Coordinates internal resources and monitors milestones to achieve service expectations. Basic Qualifications:
Experience
Minimum three (3) years of experience in a high-volume clinical laboratory.
Education
Bachelors degree in clinical laboratory science or related field required, OR four (4) years of experience in a directly related field.
High School Diploma or General Education Development (GED) required.
License, Certification, Registration
Clinical Laboratory Scientist License (California)
Additional Requirements:
Knowledge of CLIA, Title 22, CAP, JCAHO, NCQA, AABB, local, state, federal regulations.
Must be able to work in a Labor/Management Partnership environment.
Preferred Qualifications:
Previous experience in a supervisory/managerial position preferred.
Masters degree preferred.
Notes:
• 3 years or duration of existing/incoming projects.
• Rotating schedule based on research and operational need.
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