Indianapolis , IN , United States
Coordinate the efforts of the division staff to maintain company quality assurance programs at all testing facilities and diagnostic technologies. Coordinate and track external and internal proficiency testing. Duties: 1)Perform genomic testing and inspections. 2)Ensures corrective action. 3)Tracks and documents various reports. 4)Provides documentation to Corporate.
Requirements: 4-5 years of laboratory experience is preferred. Experience with USA FDA GLP regulations required. Must have at least 3 - 5 years overall experience and possesses excellent interpersonal skills.Candidate should be ASCP certified MT or equivalent.
• EDUCATION: B.A. or B.S. Degree in Chemistry
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