Roland Jbeily, MSc, DESS
Regulatory Affairs Specialist III @ Bio-Rad Laboratories
About
10+ years of experience in the pharmaceutical and medical devices industry including a broad experience in the Canadian regulatory environment. Demonstrated experience in filing pre-market and post-market regulatory submissions for a wide portfolio of products. Demonstrated technical knowledge of Chemistry, Manufacturing and Control (CMC). Skilled in technical writing and presentation skills (published article in Contract Pharma) and performed professional global webinars. Skilled in Leadership (edX, Harvard University and Development Dimensions International), in GCP/GLP, ESG and continuous improvement.
Canada
Montreal
Pharmaceuticals
Regulatory Documentation, Investigational New Drug Application (IND), Microsoft Excel, Consulting, People-Oriented, Interpersonal Communication, International Regulations, Attention to Detail, Regulatory Policy, Regulatory Agencies, Gap Analysis, Multilingual, Pharmaceutical Chemistry, Stakeholder Engagement, Natural Health Products, Artwork, Regulatory Filings, Customer-Focused Service, Contract Research Organization (CRO), Thinking Skills
Experience
Roland Jbeily, MSc, DESS's Contact Information
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