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Mahgol Maroufi
Senior QA/QC Specialist in IVD, biotech and GMP/ISO 13485 compliance
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About
Quality professional with QC technician and QA experience across medical devices and pharmaceutical manufacturing (contract and direct hire). Has hands-on experience preventing shipping/packaging/labeling defects by tightening work instructions and documentation, and driving investigations/CAPA using 5 Whys and tools like TrackWise and DocuSign. Comfortable commuting to Beverly Hills and targeting $40–$50/hr.
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Key Strengths
- Prevented packaging/labeling shipment errors by revising work instructions and related documentation
- Structured root-cause investigations using 5 Whys and cross-functional evidence reviews
- CAPA and nonconformance initiation through to review/approval in QMS workflows
- Strong GMP documentation capability (SOPs, WIs, batch records, training docs) with version/standards alignment
- Hands-on experience across multiple manufacturing stages (in-process, final inspection)
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