Regulatory Affairs Project Manager @ (October 2017 - March 2020)
Senior Regulatory Affairs Specialist @ (May 2013 - October 2017)
Senior Learning and Development Specialist @ Medtronic (January 2005 - January 2013)
Training Specialist @ Chanelle (January 2004 - January 2005)
Training Co-ordinator and Training Instructor @ (July 1996 - October 2004)
Alice Forde Education
University of Galway
Postgraduate Specialist Diploma in Medical Device Science
2014-2015
University of Leicester
MSc (HRD & Performance Management)
Alice Forde Skills
21 CFR
Auditing
Authentication
CE marking
Change Control
Coaching
Coaching & Mentoring
Code of Federal Regulations
Communication
Continuous Improvement
Design Validation
Design of Experiments
Driving Results
EU MDR
Employee Learning & Development
Employee Relations
Establishment Registration
FDA
GMP
Global Regulatory Strategy
ISO 13485
Japan Regulatory Requirements
Lean Manufacturing
Manufacturing
Manufacturing Processes
Medical Device Directive
Medical Devices
Mitigation Strategies
Organizational Change Agent
Organizational Development
Organizational Leadership
PMA
Process Improvement
Process Validation
Project Management
Quality System
Regulatory Advocacy
Regulatory Approvals
Regulatory Requirements
Regulatory Submissions
SAP
Six Sigma
Team Building
Training
U.S. Food and Drug Administration (FDA)
Validation
Vascular
Vigilance reporting
u.s. Food and Drug Administration Fda
u.s. Food and Drug Administration
Alice Forde Summary
Alice Forde, based in Ireland, is currently a Senior Director, Global Regulatory Affairs - Vision Care, Regulatory Info Management and RegIntel at Bausch + Lomb. Alice Forde brings experience from previous roles at Bausch + Lomb and Teleflex Incorporated. Alice Forde holds a 2014 - 2015 Postgraduate Specialist Diploma in Medical Device Science @ University of Galway. With a robust skill set that includes 21 CFR, Auditing, Authentication, CE marking, Change Control and more. Alice Forde has 2 emails and 2 mobile phone numbers on RocketReach.
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