• R&D Projects and Document Supervisor

    Job Functional Area
  • Overview


    IVC is proud to be an Equal Opportunity Employer  M/F/D/V - EOE.  International Vitamin Corporation (IVC) is a leading global manufacturer of vitamins and nutritional supplements with more than half a century of private label and contract manufacturing experience, an impeccable quality and regulatory compliance record, and with new resources focused on enriching the health and lives of others. We currently have an opening for a R&D Projects and Document Supervisor in our Greenville, South Carolina facility.

    The candidate for this position will ensure all required documentation has been received for any new or alternate raw materials. This candidate will work with R&D Director, Marketing and new development teams to organize and coordinate projects from NPD deliverable, formulation, scale-up and stability, until project launch. Support for Label Compliance and Regulatory Affairs. Perform research and development activities associated with formulating and reformulating solid-dose nutritional products for both international and domestic.


    • Coordinate development of ingredient documentation and macronutrient information to support new or reformulated product development
    • Organize, coordinate, and track projects for R&D and Support Quality so that departmental efficiencies are optimized.
    • Provide technical support to internal and external customers as required
    • Request information from raw material and bulk product suppliers to develop and maintain internal databases of information to support label copy development
    • Prepare, review and issue accurate R&D technical documentation, including Master Formulas Documents (MBR's), reports and other.
    • Review formulas, paper formulas for costing, and raw material documents to support new business opportunities.


    • Bachelor in Chemistry/Pharmaceutical sciences with 5-10 years experience in Pharmaceutical sciences preferred.
    • Strong working knowledge in a solid dosage Dietary Supplement environment
    • Strong working knowledge of cGMPs
    • Some experience operating R&D Scale blending, compression, and coating equipment
    • Display full understanding of technical requirements for commercialization of Dietary Supplement Products
    • Experience must reflect strong regulatory capabilities and commitment to excellence
    • Advanced knowledge of the principles, concepts and practices of formulation and product development of solid dose forms of nutritional dietary supplements.
    • Applies technical, functional & industry knowledge to design experiments, lead and organize multiple projects
    • Regularly develops/creates new hypotheses using originality and knowledge
    • Understands the process of development and labeling of dietary supplements
    • Identifies and develops scientific activities to support short and mid term operational goals
    • Influences the project team by providing formal/informal mentoring and coaching


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