Quality is in our DNA -- is it in yours?
You are made of leadership material. You have proven people skills, a passion for patient care, and the drive to succeed. You're also looking for great benefits, the support of an all-star team, and an opportunity to grow your career.
Join our front line of #HealthcareHeroes! Our mission is to advance the health and wellbeing of our communities as a leader in Clinical Laboratory solutions.
This opportunity is:
Location: Dallas, Texas (75247)
Days: Monday - Friday
Hours: 9:00 AM - 5:00 PM
Full-time: Benefit Eligible
Operations
- Compile, review, and/or coordinate the collection of accurate laboratory data and key indicators to monitor the quality/process improvement and efficiency/workload of the department and personnel.
- Evaluate the department's performance against the established key indicators, making and recommending process changes to enhance efficiency and quality.
- Implement/utilize workload monitoring and reporting system to maintain optimal work-schedule for staff as well as to prepare justifications for adjustments to staff.
- Resolve technical problems in accordance with policies and procedures established by the laboratory manager or technical supervisor.
- Troubleshoot quality and production issues relating to equipment, processes and systems. Ensure that remedial actions are taken when test systems deviate from the laboratory's established performance specifications.
- Maintain areas of responsibility in constant state of inspection readiness, ensuring that standard operating procedures (SOP's) accurately reflect the current processes, and that all required records - competence assessment, maintenance, logs, etc. - are kept current at all times.
- Oversee quality and maintenance records and activities for equipment.
Supervisory
- Manage, optimization and approval of department work schedule designed to meet business need.
- Train new employees.
- Ensure and document staff's review of and compliance with standard operating procedures (SOP's), including all safety regulations relating to personal protective equipment (PPE) and company policies
- Plan, assign and direct work in the laboratory.
- Conduct regular staff meetings and use other formal and informal communication methods to facilitate group communication as well as inform staff on relevant matters including company business and policies and procedures.
- Delegate duties when appropriate and ensure understanding of assigned duties.
General
- Attend and participate in all company sponsored or provided training.
- Maintain compliance with company and department policies and procedures.
- Maintain compliance with federal and state regulations.
- Maintain confidentiality of employee, patient, client, and/or company records and issues.
EDUCATION/KNOWLEDGE:
Bachelor's Degree in Science. ASCP or other equivalent certification required. Knowledge of Clinical Laboratory practice, specimen processing, complex sample preparation and operation of automated and semi-automated instrumentation. Excellent organizational, oral and written communication, math and computer skills required. Knowledge of and ability to interact with laboratory computer systems. Must be qualified as General Supervisor for high complexity testing under CLIA regulations.
EXPERIENCE:
Must have minimum six years of pertinent Clinical Laboratory experience subsequent to the BS degree.. Two years of supervisory duties preferred, this can be met with group leader position or equivalent.
Company:
Sonic Anatomic Pathology
Scheduled Weekly Hours:
40
Work Shift:
Job Category:
Laboratory Operations
Company:
ProPath Services, LLC
Sonic Healthcare USA is an equal opportunity employer that celebrates diversity and is committed to an inclusive workplace for all employees. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, age, national origin, disability, genetics, veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.