Richard De La Cruz Jr.
With four years in the Medical Device industry, RJ De La Cruz has strong experience in the FDA regulated industry, having performed quality across ten product lines from surgical tools to Hemodialysis Machine software. He has experience in new product development as well as DHF Remediation. Richard excels at standards analysis and compliance, verification and validation testing, and statistical analysis.
Academic & Professional Qualifications:
- B.S. Criminology, Florida State University
- Certified ISO 13485 Internal Auditor
- Certified ISO 14971 Risk Management
Training, Quality Systems, & Specialties:
Medical Device Directive (MDD)
European Medical Device Regulation (EU MDR)