Beverage Document Control Specialist

BLUE CHIP GROUP LLC•Salt Lake City, UT

About The Position

The Document Control Specialist authors, formats, tracks, stores, reviews, updates, and maintains control over Quality Assurance documentation. The role supports document accuracy, quality, and integrity by working with other departments and maintaining document control processes, systems, and databases. The position is based in Salt Lake City, Utah, and is full time. The salary range is undisclosed.

Requirements

  • 1–3 years of experience in QC dietary supplements, document control, science, engineering, technical writing, or a combination of these areas.
  • Advanced written and verbal communication skills.
  • Strong attention to detail.
  • Strong problem-solving skills.
  • Sound time-management and prioritization skills.
  • Ability to work well with various departments in the company.
  • Proficiency with Microsoft Office programs, including Word, Excel, and PowerPoint.
  • Self-starter.

Nice To Haves

  • Technical training in document control, QC dietary supplements, science, or technical writing.

Responsibilities

  • Process documentation for new and existing MMRs.
  • Work with other departments to build, review, and maintain documents, ensuring their accuracy, quality, and integrity.
  • Develop and maintain document control processes and systems.
  • Maintain the raw materials/components database.
  • Maintain files and retrieve requested documents for inspections, audits, traceability exercises, recalls, market withdrawals, and business continuity.
  • Perform other duties as assigned.
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