Job Description
This position will be responsible for assisting in monitoring key quality activities and processes for Greenwood Genetic Center Diagnostic Laboratories under the direction of the Quality Assurance Manager.
These duties include analyzing Molecular, Biochemical, and Cytogenomic laboratory statistical quality reports, to ensure laboratory regulatory standards are being met.
Activities relating to the operations of these departments may also include monitoring regulatory requirements in the categories of safety, electronic records, personnel, databases, specimen management, record retention, patient data, interfaces, HIPAA, results reporting, reagents, instrumentation, test methods and validation, maintenance, etc.
The Quality Improvement Assistant will assess findings and suggest improvements based on patient safety goals.
Qualifications:
- BS degree in biology, chemistry, or life sciences
- ASCP Certification preferred
- Previous experience in diagnostic laboratory workflows/analysis.
Job Summary
Contacts
Phone: 864-941-8100Similar Jobs
The largest community on the web to find and list jobs that aren't restricted by commutes or a specific location.
-
Chemistry Technician III 3rd Shift
- Bausch + Lomb
Conducts chemical and physical tests on chemical raw materials, in-process and finished products using qualitative and quantitative techniques.
-
Chemistry Technician III Weekend Nights
- Bausch + Lomb
Conducts chemical and physical tests on chemical raw materials, in-process and finished products using qualitative and quantitative techniques.
-
Regulatory Manager
- Rhythmlink International LLC
Responsible for overseeing the company's compliance with current and future regulatory requirements. Duties include proper activities for regulatory compliance with US and International requirements including regulatory submissions and licensing, representation during design and development activities, and internal and external support during audits. Manage the ECO/ECN process, generation and maintenance of technical documentation, and the Vigilance forms and process.