Kendal Dinsmore

About Kendal Dinsmore

SUMMARY OF QUALIFICATIONSASQ Certified: CMQ/OE. Trained to develop and integrate sustainable organization quality and regulatory compliance from strategic planning to implementation. Can conceptualize and communicate the big picture while fulfilling day-to-day activities necessary for successful performance improvement. Understanding of the communication needs of all staffing levels from strategic to tactical. Possess strong experience in fostering and developing key business relationships. Key strengths include: Start Ups QMS Implementation from scratchCLIA / ISO 13485 / ISO 17025 / ISO 62304 / QSR cGMP Root Cause Analysis / CAPA / Lean / Six SigmaCustomer Focus and Satisfaction Project ManagementContinuous Performance improvement Supplier Quality ManagementDe Novo and 510(k)

Experience

1. VP, Regulatory Affairs & Quality Assurance

   Updoc

   Mar 2025 — Present · San Francisco, CA, US

Education

• UCSC extension

  Regulatory Affairs

• Pepperdine Graziadio Business School

  Master of Business Administration (MBA)

  2003 — 2005

• Sonoma State University

  BA, Biology

  1992 — 1993

Skills

• Start-Ups
• Good Laboratory Practice (Glp)
• Glp
• Lean Manufacturing
• Cross-Functional Team Leadership
• Process Validation
• R&D
• Iso 13485
• Process Improvement
• Business Process Improvement
• Sop
• Fda
• Root Cause Analysis
• Medical Devices
• Capa
• Quality Management
• Regulatory Affairs
• Lifesciences
• Design Control
• Quality Control
• Gmp
• Quality Assurance
• Quality System
• Quality Systems
• V&V
• Life Sciences
• Document Management
• Standard Operating Procedure (Sop)
• Spc
• Statistical Process Control (Spc)
• Corrective and Preventive Action (Capa)
• Validation
• Verification and Validation (V&V)
• Change Control
• U.s. Food and Drug Administration (Fda)
• Design of Experiments
• Manufacturing
• Continuous Improvement
• Compliance
• Six Sigma