• Establish and monitor systems, policies, and procedures for alignment with regulatory compliance requirements for cosmetics and NHPs, knowledge of Health Canada's Food and Drugs Act and FDA's Food, Drug and Cosmetics Act to ensure formulas, packaging and claims meet market specific regulations.• Work with third parties to ensure compliance of formulas, packaging and claims meet global standards (EU, Middle East, China, Southeast Asia, Australia)• Provide regulatory information to the… Show more • Establish and monitor systems, policies, and procedures for alignment with regulatory compliance requirements for cosmetics and NHPs, knowledge of Health Canada's Food and Drugs Act and FDA's Food, Drug and Cosmetics Act to ensure formulas, packaging and claims meet market specific regulations.• Work with third parties to ensure compliance of formulas, packaging and claims meet global standards (EU, Middle East, China, Southeast Asia, Australia)• Provide regulatory information to the business team ensuring regulatory compliance within specified markets and develop strategies to anticipate future changes• Oversee ongoing regulatory and quality assurance activities including issuance of ILS, letters of compliance, Certificates of Free Sale, safety assessments; develop and conduct programs to maintain quality standards of raw materials and finished products within Blacklist restrictions• Effectively provides support when necessary to R&D, marketing, sales and logistics to ensure timely procurement and distribution of goods Show less

• Effectively managed over 5 files daily assessing scientific and proprietary information including sensitive requests pertaining to confidential business information• Created detailed reports to relay scientific information sourced from various drug submission and clinical trial applications (DIN, NDS, SNDS, ANDS, CTA etc.) to the Corporate Services Branch and made recommendations on technical and confidential business information that should be exempted from release to applicants based… Show more • Effectively managed over 5 files daily assessing scientific and proprietary information including sensitive requests pertaining to confidential business information• Created detailed reports to relay scientific information sourced from various drug submission and clinical trial applications (DIN, NDS, SNDS, ANDS, CTA etc.) to the Corporate Services Branch and made recommendations on technical and confidential business information that should be exempted from release to applicants based on the Access to Information Act• Prepared and presented training slides on new SOPs to team members and offices of primary interest (OPIs) including TPD, MDD, VDD, NNHPD, PPIAD, MHPD,FD ONPP• Participated in team meetings and working group meetings with other divisions and produced records of information and decisions• Successfully took the lead and completed two complex files on Third Party Objections (TPOs) and Judicial Reviews (JRs) Show less

• Entrusted with keyholder responsibilities, managing client’s medical history and onboarding new receptionists• Educated clients on skin and nail health products to consistently exceed a monthly sales goal resulting in increased revenue• Maximized the capabilities of the company’s software to create a more streamlined method of tracking promotions purchased and client's insurance information for processing payments more efficiently

• Assisted various graduate students on projects using functional material components to create stretchable electronics and with developing and characterizing new self-assembled monolayers• Entrusted to train incoming undergraduate students in basic laboratory safety and procedures• Used Microsoft Excel and PowerPoint to organize experimental data into graphs ready for presentation and publication

Keyholder position responsible for opening and closing procedures, keeping area well stocked and cleaned, preparing orders and completing POS transactions.