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Shift:

8:00 AM to 4:30

PM Duties & Responsibilities:

Quality Documentation Specialist - Duties Manage and maintain quality documents, including SOPs, BPRs, COAs, specifications, and certifications. Administer the Change Control process and ensure proper approvals. Scan, organize, file, and maintain controlled documents. Review and update documents to meet

FDA, NSF

GMP, SQF, and company standards. Support internal, customer, regulatory, and third-party audits. Provide quality documentation promptly while maintaining accuracy and confidentiality.

Requirements & Qualifications:

Associate's degree in a related field preferred 3+ years of document control or related experience Strong attention to detail and accuracy Proficient in Google Workspace and Microsoft Office, including Excel and Word Knowledge of regulatory documentation requirements preferred Knowledge of NSF and SQF standards for food and dietary supplements preferred Strong written and verbal communication skills Able to manage multiple priorities and meet deadlines Self-motivated and able to work independently in a fast-paced environment Must maintain confidentiality and handle controlled documents with integrity Join us as a Doc Control Specialist to play a vital role in maintaining our commitment to quality excellence! Bring your expertise in document management systems, regulatory standards, and organizational skills to help us deliver top-tier products while advancing your career in a vibrant environment dedicated to innovation and compliance.

Pay:

$17.00 per hour

Language:

English and Spanish (Preferred)

Work Location:

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Find & Apply For Switchboard / Telephone Operator Jobs in Vineyard, Utah

QA Doc Control Specialist