Roberta França

Senior Regulatory Affairs Program Lead at Johnson & Johnson

Role
Senior Regulatory Affairs Program Lead at Johnson & Johnson MedTech
Location
Dallas-Fort Worth, TX, US
LinkedIn followers
500 followers
Healthcare & Human ServicesView LinkedIn profile

About Roberta França

RA Professional certified by RAPS with RAC (Global). Over 15 years of experience in…

Experience

  1. Senior Regulatory Affairs Program Lead

    Johnson & Johnson MedTech

    Sep 2022 — Present · Dallas-Fort Worth, TX, US

    As part of Ethicon Endo Surgery Global RA team, I’m representing the RA Business Unit in product life cycle projects related to packaging changes.I’m also supporting the implementation of new regulations as such as UKCA for Ethicon Endo Surgery Products.Beyond that I’m supporting the conclusion of Multivariant project, which has been requiring a deep evaluation of product data, worldwide license data, and investigation of back-order causes in a time manner.

Education

  • Universidade Federal de Minas Gerais

    Pharmacist

    2004 — 2009

Skills

  • Project Management
  • Management
  • Product Launch
  • Teamwork
  • Software Documentation
  • Microsoft Excel
  • Gmp
  • Regulatory Affairs
  • Manufacturing
  • Cross-Functional Team Leadership
  • Microsoft Office
  • Strategic Planning
  • Medical Devices
  • Strategy

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Roberta França — Senior Regulatory Affairs Program Lead at Johnson & Johnson MedTech in Dallas-Fort Worth, TX, US | Unifers