Rocco Bravoco

About Rocco Bravoco

Accomplished Quality Engineer and Manager with over 9 years experience in Quality and Regulatory in the Medical Device industry. Strong background with ISO 13485, 21 CFR 820, Medical Devices, CAPA, Process Validation, and Equipment Controls. Demonstrated a successful history of managing internal audits, FDA inspections, and 3rd party audits by Notified Bodies. Excellent problem solving, multi-tasking, and prioritizing skills.

Experience

1. Senior Manager - Integrated Signal Management Engineering - Complaints Trending

   Amgen

   Feb 2022 — Present

Education

• Rowan University

  Bachelor of Science (B.S.)

  2005 — 2009

Skills

• Microsoft Office
• Sales
• Sales Operations
• 21 Cfr Part 820
• Sales Management
• Customer Service
• U.s. Food and Drug Administration (Fda)
• Manufacturing
• Medical Devices
• Product Launch
• Project Management
• Solidworks
• Microsoft Excel
• Strategic Planning
• Inventory Management
• Microsoft Word
• Team Management
• Engineering
• Team Building
• Management
• Continuous Improvement
• Process Improvement
• Sales Process
• Contract Negotiation
• Start-Ups
• Fda
• Training
• New Business Development
• Quality System
• Business Development
• Corrective and Preventive Action (Capa)
• Cross-Functional Team Leadership
• Lean Manufacturing
• Leadership
• Iso 13485
• Product Development
• Quality Management