Annie Huang
Regulatory Affairs Specialist @ Zimmer Biomet
About
Detail-oriented regulatory affairs graduate specializing in medical device regulations seeking to apply expertise in facilitating and coordinating global regulatory assessments for medical devices. Eager to contribute strong project management abilities and regulatory knowledge to support regulatory initiatives.
United States
Los Angeles
Medical Device
Regulatory Intelligence, Regulatory Guidelines, Regulatory Analysis, Data Analysis, Data Management, Python (Programming Language), Qualitative Organic Analysis, Wet Labs, Mathematical Modeling, MATLAB, Java, Project Management, Regulatory Submissions, Regulatory Compliance, U.S. Food and Drug Administration (FDA), Regulatory Affairs, Computer Literacy, Problem Solving, Microsoft Excel, Analytical Skills
Experience

Regulatory Affairs Intern
Los Angeles, California, United States
D.K. Kim International Center for Regulatory Science at USC Mann School of Pharmacy and Pharmaceutical Sciences provides regulatory expertise, advice and services to its faculty with new grants, start-up companies with interesting products, and anybody else who might need help navigating the complex global regulatory environment.

Regulatory Affair Intern | USC TRAQS Program
The Team-based Regulatory And Quality Solutions Program (TRAQS) is an experiential project program for MS Regulatory Science at USC. Team members will work with sponsoring companies on projects which address important objectives of the sponsoring firm.

Research And Development Intern
New Taipei City, New Taipei City, Taiwan
- Assisted in GMP manufacturing of drug substances (ex. buffer/media preparation, weighing raw materials, tablet hardness and friability testing, wet and dry granulation, dissolution testing, tablet film coating, tablet pressing, tubing preparation) - Analyzed compounds to determine chemistry or physical properties, composition, etc. using chromatography, GC/MS, and spectrophotometry techniques
Annie Huang's Contact Information
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