Jacquelyn Hughes

Director Post Market Surveillance at Zimmer Biomet

Role
Director Regulatory Affairs and Clinical Research at Biomet 3i
Location
Palm Beach Gardens, FL, US
LinkedIn followers
500 followers

Experience

  1. Director Regulatory Affairs and Clinical Research

    Biomet 3i

    Mar 2012 — Present · Palm Beach Gardens, FL, US

    Team members in FL and in Europe for both RA and CR. Global registrations and clinical trials.

Education

  • Fairleigh Dickinson University-Metropolitan Campus

    BA, Economics

    1981 — 1983

Skills

  • Iso
  • Pharmaceutical Industry
  • Sop
  • Fda
  • Lean Manufacturing
  • Biotechnology
  • Product Development
  • Technology Transfer
  • Quality System
  • V&V
  • Regulatory Affairs
  • Lifesciences
  • Orthopedic
  • Urology
  • Iso 13485
  • Product Management
  • 21 Cfr Part 11
  • Cardiology
  • Regulatory Requirements
  • Six Sigma
  • Product Launch
  • Quality Auditing
  • Process Improvement
  • Strategy
  • Commercialization
  • Hardware Diagnostics
  • Capital Equipment
  • Quality Assurance
  • Quality Control
  • Gmp
  • Competitive Analysis
  • Start-Ups
  • R&D
  • Market Development
  • Design Control
  • Clinical Trials
  • Strategic Planning
  • Regulatory Submissions
  • Validation
  • Cross-Functional Team Leadership

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Jacquelyn Hughes — Director Regulatory Affairs and Clinical Research at Biomet 3i in Palm Beach Gardens, FL, US | Unifers