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Laboratory Quality Specialist Jobs
Company | Nucleus Healthcare |
Address | Armstrong, MO, United States |
Employment type | FULL_TIME |
Salary | |
Category | Staffing and Recruiting |
Expires | 2023-06-17 |
Posted at | 11 months ago |
Nucleus Healthcare is seeking a qualified Laboratory Quality Specialist candidate to join a prestigious academic health system in Columbia, MO. Take the next step in your career and thrive in an environment where you are respected, challenged, and offered endless opportunities to define your career path!
- “Just Culture” organization
- Becker Healthcare's 150 Top Places to Work
- Prestigious public university
- Public schools
- Healthcare system
- Affordable cost of living and housing
- Division 1 sports
- Up to 75% for you and 50% for spouses and children
- 100% paid leave for parents and caregivers for up to four weeks – effective January 2024
- Comprehensive health and wellness benefits, including mental health support
- Defined career paths and laboratory
- Generous retirement program– 8% match on 401k!
- Paid-for tuition from the local top-rated university
- Includes all locations and online
- 5+ Years: 22 Days
- 0-5 years: 17 Days
- 4 Days
- 12 Days
- Up to $111,426/ year based on experience
- Monitor and update policies and procedures to be compliant with accrediting agencies.
- Prepare, participate, and respond to required accreditation inspections and implement corrective actions.
- Responsible for the preparation of equipment and process validation protocols, documentation of results, statistical analysis, generation of reports, and ensuring appropriate validation before implementation.
- Support the functions of the main MU Health Care laboratories as needed.
- Function as a backup for all Cellular Processing Laboratory processes.
- Prepare departmental reports for presentation. Communicate trends and opportunities for improvement to key process owners.
- Review manuals annually.
- May complete unit/department-specific duties and expectations as outlined in department documents.
- Lead development and auditing of quality systems that ensure compliance, excellence, and efficiency.
- Review new and revised standards and checklists from CAP, CLIA, DNV, FACT, etc.
- Perform process for documentation, investigation, and reporting of adverse reactions or events during cell therapy product collection or infusions.
- Monitor and perform supplier qualification, supplier monitoring processes, environmental control, and monitoring systems.
- Review and report system or product deviations to appropriate internal and external parties.
- We are fueled by passion and purpose
- We are ONE team
- We are change agents
- We are precise
- We are committed
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