Back to home page
Medical Industry
Extensive experience in Process Development and Factory Operations with seven years of work in the medical device industry.  Accomplishments have demonstrated a consistent record of reducing costs by continuously driving corrective actions that yield higher quality, improve methods and enhance manufacturing operations.

  • Auditor - Conduct internal audits for compliance with ISO 13485 Medical Device Standard and Canadian CMDCAS
  • Process Validation per Good Manufacturing Practices (GMP) - 21 CFR 820.75 QS/GMP
  • Basic Science Diplomate - Human factors, Biomechanics and Ergonomics. 
  • X-ray positioning, reading and technology
Return Home