- Monitors, reports, and audits the DaVita Labs Quality Management System and Quality Assurance programs in accordance with Federal and State regulations, Clinical Laboratory Improvement Agency (CLIA) and Good Clinical Laboratory Practices (GCLP).
- In collaboration with clinical laboratory lane leaders and teammates identifies opportunities, develops, plans, and executes projects to ensure Continuous Quality Improvement and alignment with GCLP guidelines as well as Federal [CMS/CLIA], State, and accrediting agency [College of American Pathologists (CAP)] clinical regulatory requirements.
- Adheres to corporate standard policies and procedures related to job performance, customer interactions, employee relations, and information confidentiality.
- Reviews and maintains technical documents supporting the clinical lab and operations.
- Acts as subject matter expert in technical area(s) supported
- Participates in transactions in accordance with standard operating procedures(SOPs) and actively collaborates in procedural reviews, seeking lane specific expertise as needed
- Reviews and monitors clinical laboratory technical documents to ensure regulatory compliance
- Collaborates with lane leaders to verify and ensure that appropriate records are maintained to document adherence to regulatory requirements
- Reviews existing laboratory and business processes to identify gaps/opportunities
- Actively engages in departmental continuous improvement/quality initiatives
- Provides guidance and continuous improvement recommendations based on both regulatory and technical knowledge
- Leads and/or actively participates in special projects to ensure quality
- Prepares and distributes reports for external partners and vendors to manage quality projects and programs.
- Reviews change requests for potential impact on quality.
- Reviews Planned Deviations and Something Happened Intake forms (SHIF) for potential impact on quality
- Reviews corrected results for potential impact.
- Provide direct QA support for laboratory operations and closely integrated functions
- Performs training and competency assessment for Technical Analyst I & II. Reviews projects, test plans, reference documents, and research articles to gain knowledge and experience.
- Investigation
- Development of corrective action/preventative action plans.
- Ensure documentation is complete and aligns with regulatory requirements.
- Perform Root Cause Analysis (RCA).
- Track/reports events and action plans
- Follow up on action plans
- Independently plans and executes audits
- Assembles and distributes audit findings
- Provide guidance for corrective action.
- Develops, compiles, and executes responses to audit findings
- Track audit findings to closure
- Monitor corrective action to completion and verify for effectiveness.
- Analyze and track metrics related to quality.
- Partner with clinical lab lanes to monitor data and provide technical recommendations on instrument validations/verifications, proficiency testing, and instrument quality control programs to ensure accurate patient testing and regulatory alignment.
- 4-6 years experience required
- Associate's degree as a Medical Laboratory Technician (MLT) or Bachelor's degree in MLS/MLT, Clinical Laboratory or Biological science required
- Minimum of four (4) years' clinical lab experience required
- Knowledge/ experience with CLIA, CAP and GCLP standards preferred
- Intermediate computers sills and proficiency in MS Word, Excel, Outlook, PowerPoint, MS Project, and Visio required
- Team leadership experience preferred
- Comprehensive benefits: Medical, dental, vision, 401(k) match, paid time off, PTO cash out
- Support for you and your family: Family resources, EAP counseling sessions, access Headspace, backup child and elder care, maternity/paternity leave and more
- Professional development programs: DaVita offers a variety of programs to help strong performers grow within their career and also offers on-demand virtual leadership and development courses through DaVita's online training platform StarLearning.
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Analyst II, Quality Technical - DeLand, United States - DaVita
Description
3000 Davita Way, Deland, Florida, , United States of America
Job Description
GENERAL PURPOSE OF THE JOB
The Technical Analyst II, QA (Lab) is responsible for the following:
More than just pay, our DaVita Rewards package connects teammates to what matters most. Teammates are eligible to begin receiving benefits on the first day of the month following or coinciding with one month of continuous employment. Below are some of our benefit offerings.
At DaVita, we strive to be a community first and a company second. We want all teammates to experience DaVita as "a place where I belong." Our goal is to embed Diversity & Belonging into everything we do in our Village, so that it becomes part of who we are. We are proud to be an equal opportunity workplace and an affirmative action employer. As such, individuals are recruited, hired, assigned and promoted without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, protected veteran status, or any other protected characteristic.
Applications are accepted on an ongoing basis.
Salary/ Wage Range
Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies and experience and may fall outside of the range shown. DaVita offers a competitive total rewards package, which includes a 401k match, healthcare coverage and a broad range of other benefits. Learn more at
