David McGrath

Vice President of Quality & Regulatory @Genalyte, Inc

San Marcos, CA, US
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Mar 2023 — Present

Vice President of Quality & Regulatory @Genalyte, Inc

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EDUCATION

1997 — 1999

University of Maryland

MS, Reliability Engineering

N/A

University of Maryland

Master of Science - MS, Reliability

1979 — 2005

San Diego State University

BSEE, Engineering

SKILLS

21 Cfr Part 11Start-UpsDesign AssuranceQuality ProceduresProcess ImprovementCommercializationMedical DevicesCapaNcmrQuality SystemV&VReliability EngineeringProject ManagementContinuous ImprovementMdrsHealthcareBiomedical EngineeringRegulatory AffairsManagement ReviewBiotechnologyQuality System CompliancePost Market SurveillanceValidationCost of QualityIso ImplementationIso 13485CmdcasCross-Functional Team LeadershipIso 14971Quality ControlGmpIsoCmdrFdaQuality ManagementLean ManufacturingManagementPart 820Design of ExperimentsManufacturing

ABOUT DAVID MCGRATH

Experienced Leader of Global Quality and Regulatory Affairs with demonstrated successful leadership and proven results in the medical device and diagnostic industries. Strong quality assurance and regulatory compliance knowledge and skills compliment my technical engineering background. Experience gained in world class companies across industries is applied to deliver world class results, now specializing in Medical Device industry- Quality Management Systems (21 CFR 820, ISO 13485:2003,2012,2016)- EU Medical Device Regulation- Global Registrations: 510k, De Novo, EUA, CE, TGA, Canada MDR- New Product Development (Design Control) Quality and Regulatory Affairs- Supplier Approval, Monitoring, Surveillance and Control- Product Safety (IEC 60601-xx)- Global Cost of Poor Quality program- Risk management ISO 14971:2019- Certified Lead Auditor (ISO 13485, MDSAP)- MDSAP Single Audit Program- Product and Process Validation and Transfer- Reliability Engineering and Statistical Expertise- Global Compliance Leader (CAPA, Complaints, Vigilance, QMS)- Management Representative for FDA and International inspections- Certified Six Sigma Black Belt- Post Market Surveillance, Clinical Evaluation, Usability, and Technical Data for Medical Device

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