Supports reagent activities in Clinical Laboratories, including incoming material inspections to ensure product safety and compliance. Non-technical role.
Responsibilities
Perform incoming inspection and reagent release
Ensure equipment and instruments are in good operating condition
Verify data entry in Laboratory Information Management System
Support workflows intra and inter-departmentally
Work cross-functionally with Team and other departments
Follow/Ensure GLP and GMP compliance
Escalate Non-Conformity
Participate in Continuous Improvement Projects
Assist in training/implementation of new process changes
Assist in planning workflow and day-to-day schedule
Conduct self in a Professional manner
Perform work with little to no supervision
Adhere to Departmental Expectations
Handle PHI regularly
Complete required training
Maintain current status on Natera training requirements
Requirements
High School Diploma or GED or equivalent
Adaptability and Flexibility
Ability to multi-task and work independently
Excellent interpersonal, communication, computer, troubleshooting, organizational, problem-solving, and technical skills
Strong time management skills
Actively seeks ways to improve quality and workflows
Willingness to learn
Ability to promote a positive Team environment
Maintain a high level of professionalism and responsibility
Basic knowledge in Data management, Google Docs, LIMS, and Continuous Improvement
Take initiative and ownership of projects/assignments with attention to detail