Description
SUMMARY Professional with extensive experience in Regulatory Affairs/Quality Assurance in the medical device, pharmaceutical and automotive industries. Managed and supported domestic and international registrations from new product development, sustaining products to rapid response products. Project Management Market Releases Letters to File International Registrations CN reviews and sign-off Finished good inspections Excel database management Regulatory Assessment Lead Quality Trainer Technical file updates Production Operator/Assembler Quality Assurance Technician/ Receiving incoming Raw Materials
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