Description
Responsibilities-Implement, develop and perform IQ/OQ/PQ
-Prepare Validation Reports
-Improve Quality System policies and procedures
-Assist in the completion of CAPAs
-Draft related Validation Reports
-Perform risk analysis/assessment of critical processes using FMEA
Required
BS degree in Engineering, Chemistry, Chemical Engineering, Biochemistry, or closely related field
2-5 years work experience for a diagnostics or medical device company.
Excellent communication skills
Eagerness to learn