Work closely with Nature’s Rule Product Development to review formula proposals to ensure that ingredients meet NFSA Standards of Evidence for Identity.
Review and approve finished scripts and is responsible for the accuracy and content for all Nature’s Rule Branded labeling
Review and approve critical elements of labeling prior to the release to the printer
Prepare registration Documents of all new products and Re-registered products.
Follow up all steps of registration with NFSA.
Maintains change control system and version control for all labeling
Interface with the document reviewers and approvers to align wording, requirements and deliverable as needed to facilitate approval process.
Calculate and review the products’ supplement facts.
Job Requirements
Bachelor’s Degree in Science, Chemistry, Biochemistry, Pharmacy, Biology, or related field.
3+ years of progressive Quality or Product Development experience in a cGMP or regulated manufacturing industry preferred
Technical writing experience in a compliance environment or a scientific environment such as microbiology, food science, chemistry or biochemistry and Quality Management System (QMS) preferred.
High degree of proficiency MS Office Suite, Outlook & Internet applications.
Solid understanding and application of mathematical concepts
Ability to develop and maintain collaborative relationships with peers and colleagues across the organization, as well as internal and external clients
Ability to work well autonomously and within a team in a fast-paced and deadline-oriented environment.
Ability to work with and influence peers and senior management
Self-motivated with critical attention to detail, deadlines, and reporting
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