Regulatory Compliance Labeling Supervisor


Creates and updates labeling documentation and product information for an assigned group of medical/recreational products in order to optimize consumer safety and minimize product liability risk. Works internally with R&D, Regulatory, Quality and other internal functional areas to ensure timely Regulatory and Quality compliance, and to support business objectives as required.


  • High school diploma/GED required
  • Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis
  • Degree in the biological or food/pharmaceutical or regulatory sciences preferred
  • 2-5 years of relevant regulated industry experience including experience in regulatory affairs is required
  • Knowledgeable of Food and Cannabis Formula guidance’s, regulations, development process, and industry standard practices is desirable
  • Proficient in written, oral, and interpersonal communications in English
  • Ability to work in close collaboration with colleagues cross functionally
  • High attention to detail; ability to organize and prioritize assigned projects
  • International experience with documentation and process of regulatory agency notifications is highly preferred
  • Proficient user of standard MS Office suite (e.g. Word, Excel), experience using electronic document management systems and document review tools desirable
  • Research and locate information on regulatory requirements and products
  • Handle detailed tasks and prioritize them
  • Meet deadlines
  • Review and analyze documentation
  • Exercise judgment and creativity within defined procedures and practices to
  • determine appropriate action
  • Develop general knowledge of technical alternatives and gain an understanding of their impact on associated products, systems and the business
  • Apply business ethical standards
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