Description
Over 14 years of experience in the Pharmaceutical and Medical Device Industry. Strong detailed and task-oriented skills. Work environment regulated by 21 CFR 820 and ISO 13485:2003 & 9001. Specialized in Quality Assurance, Regulatory Compliance, GMP, Document Control, QSR training, Excel, Power Point, Microsoft Word, Agile, Master Control System, QCBD. ASQ Inspector Certified, Lead Auditor Certified, Technical Seminar: Improving Inspection Effectiveness and Bio-Technology Training.
Work Experience
| COMPANY | POSITION HELD | DATES WORKED |
|---|---|---|
| Stallergenes Greer | Quality Assurance Associate Ii / Sr. Document Control Quality Assurance Compliance Assistant | 5/2017 - 5/2017 |
| South West Greene Int'l | Quality Assurance Associate/ Document Control Coordinator | 10/2013 - 6/2016 |
| Scantibodies Inc. | Quality Inspection Supervisor | 7/2013 - 10/2013 |
Accomplishments
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