2005 -
2008 Regulatory Affairs Manager @ Bomac Research Limited
2003 -
2005 Regulatory Affairs Officer @ Bomac Research Limited
Michael Syme Education
University of Auckland
Master's degree
2001
-
2003
The University of Auckland
Bachelor's degree
1995
-
1998
Michael Syme Skills
Regulatory Affairs
Regulatory Submissions
Pharmaceutical Industry
Regulatory Requirements
eCTD
CTD
Regulatory Intelligence
CMC Regulatory Affairs
Regulatory Documentation
Pharmaceutical Research
SOP
Pharmaceutics
GMP
Regulatory Guidelines
European Union
Team Leadership
Validation
Bioequivalence
Pharmacology
Clinical Trials
GLP
Technology Transfer
Clinical Pharmacology
Team Building
European Law
Team Management
Employee Training
Performance Reviews
Global Regulatory Compliance
CMC development
Pharmacokinetics
Management
Document Review
Meet Deadlines
Managing Deadlines
Patent Searching
Databases
Coaching Staff
Report Writing
Technical Writing
Electronic Common Technical Document (eCTD)
Standard Operating Procedure (SOP)
Cloud Applications
Project Implementation
Good Laboratory Practice (GLP)
Good Laboratory Practice Glp
Public Speaking
Sales
Creative Writing
Customer Service
Electronic Common Technical Document Ectd
Standard Operating Procedure Sop
Project Management
Public Relations
Food Quality
Food Industry
Supplemental Health
Food Manufacturing
Dietary Supplements
Electronic Common Technical Document
Standard Operating Procedure
Good Laboratory Practice
Nutraceuticals
Michael Syme Summary
Michael Syme, based in Auckland, NZ, is currently a Regulatory Affairs Manager at Vitaco Health Group. Michael Syme brings experience from previous roles at Douglas Pharmaceuticals Limited and Bomac Research Limited. Michael Syme holds a 2001 - 2003 Master's degree @ University of Auckland. With a robust skill set that includes Regulatory Affairs, Regulatory Submissions, Pharmaceutical Industry, Regulatory Requirements, eCTD and more. Michael Syme has 1 emails on RocketReach.
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