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Erric Widjaja Location
Los Angeles, CA, US
Erric Widjaja Work
Principal Regulatory Affairs Specialist @ (June 2025 - Present)
Manager Global Regulatory Affairs @ (September 2021 - February 2025)
Manager Regulatory Affairs @ (January 2021 - September 2021)
Staff Regulatory Affairs @ (April 2015 - January 2021)
Sr. QA and Regulatory Affairs Specialist @ (January 2014 - March 2015)
Sr. Regulatory Affairs Specialist @ (May 2011 - July 2013)
Regulatory Affairs Specialist @ (November 2010 - May 2011)
Regulatory Technical Specialist III @ (March 2004 - November 2010)
QA Specialist @ (February 2002 - March 2004)
Erric Widjaja Education
California State University-Northridge
BSc
Erric Widjaja Skills
FDA
Regulatory Affairs
Design Control
ISO 13485
V&V
Medical Devices
Change Control
LIMS
R&D
Quality System
GLP
CE marking
Quality Assurance
Lifesciences
21 CFR Part 11
Validation
ISO 14971
CAPA
GMP
Biotechnology
Sop
21 CFR
Biopharmaceuticals
Quality Control
FDA GMP
ISO
Microbiology
Hardware Diagnostics
Regulatory Submissions
Technology Transfer
Oncology
ELISA
Quality Auditing
Commercialization
Complaint Management
Pharmaceutical Industry
PMA
GxP
CTMS
Laboratory
Root Cause Analysis
GCP
HPLC
Product Launch
Regulatory Requirements
Infectious Diseases
CQA
Document Management
Biomedical Engineering
Assay Development
Regulatory
Erric Widjaja Summary
Erric Widjaja, based in Los Angeles, CA, US, is currently a Principal Regulatory Affairs Specialist at New World Medical. Erric Widjaja brings experience from previous roles at HOYA Surgical Optics, NanoString Technologies, Inc., Beckman Coulter Diagnostics and DxTerity. Erric Widjaja holds a BSc @ California State University-Northridge. With a robust skill set that includes FDA, Regulatory Affairs, Design Control, ISO 13485, V&V and more. Erric Widjaja has 2 emails and 2 mobile phone numbers on RocketReach.
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