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Job Description
- 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.
- Strong analytical, prioritizing, interpersonal, problem-solving, presentation, & planning skills.
- 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
