Regulatory Affairs Specialist - Vancouver, British Columbia
4 weeks ago
+ Identify compare and interpret relevant Acts Regulations associated Guidance eg Canadian FD Act US FD C Act CPSA CPLA Textiles Labeling Act etc applying them towards business activities e g concept evaluations product copy Product Master Guidelines finished product labels promotional advertising materials ensuring accuracy compliance with applicable Canadian US regulations marketing authorization of that product to minimize risk impact to the business
+ Record maintenance to support maintain the creation both team cross functional SOPs submission templates files controlled documentation regulatory product ingredient databases technical resources related legislation regulations guidelines support Saje portfolio products.
+ Product vigilance Perform product deficiency-risk assessments post-market filing consumer incident reports government agencies recalls maintenance compliance reports logs communicating management/mitigation strategies cross-functional team members.
The Regulatory Affairs Specialist is responsible for leading executing project managing regulatory activities throughout the lifecycle development licensure launch post-market maintenance extensive portfolio Natural Health Products NHPs Dietary Supplements DS OTC Non Prescription Drugs OTCS Cosmetics CA/US Consumer Products CA/US medical devices.
Job description
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