Coordinate the efforts of the division staff to maintain company quality assurance program at all testing facilities and diagnostic technologies. Coordinates and track external and internal proficiency testing. - Perform genomic testing and inspections. - Ensures corrective action. - Tracks and documents various reports. - Provides documentation to Corporate.
Requirements: 4-5 years of experience. Knowledge of USA FDA GLP regulations with laboratory experience is preferred. 3 - 5 years experience and possesses excellent interpersonal skills. Candidate should be ASCP certified MT or equivalent.