Helping Brands move upstream in their Product Licensing Journey and expanding product portfolio in the Canadian market.With expertise in the following areas:-Quality Assurance (Pharmaceutical, Health-care, Personal-care and Natural Health Product/Dietary Supplement industries)-Expert in product registration in international marketsRaw Material and Finished Product Release, BPR Review, CAPA Management, Investigating OOT and OOS & Report Findings, Document Change Control, Change Control Management, Product Development and Continuous Process Improvement, Lead Departmental Self Inspection, Annual Product Review/Product Quality Review, Maintain Quality Matrix Trend, Document Customer Complaint, Supplier Audits, Supplier Quality Monitoring, Stability Management as per ICH Q1 Guidelines and Lab-ware LIMS.-Regulatory Affairs (Pharmaceutical, Health-care, Personal-care and Natural Health Product/Dietary Supplement industries).Document Management according to cGMP guidelines, Establishment Licence/Site Licence, DIN Application, Finished Product Certificate of Analysis, Product Licence Applications for Natural Health Products, Dietary Supplements & Personal-care Products and Assist International Customers with Product Registration in International Markets.-Soft SkillsExceptional Work Ethic, Self-motivated with excellent Interpersonal/communication skills, Task-driven with strong project management skills, Capable of managing multiple projects concurrently and effectively to meet business demands.Specialties: Certified Quality Auditor, GMP, GDP, CAPA Management, Raw and Finished Product Release, BPR Review, Labels Review, Maintenance of Product Master Documents, Product Quality Review, Document Change Control, Change Control Management, Customer Complaint, Annual Product Review, Stability Management, Labware LIMS, Managing Quality Matrix and Supplier Audit.