Byheart
Quality Document Control Specialist
Allerton, Iowa, United States
Sponsorship not specifiedDetected 83 days ago
ComplianceSalesforceCRMExcelRecruitingGMPFDA RegulatoryCommunicationProblem SolvingWritingFood SafetyFood ScienceRegulatory Affairs
About the role
- High focus on reviewing, editing, and releasing GMP documentation.
Responsibilities
- Manages the Document Control System, manually or through programs such as Dot Compliance(a Salesforce-based electronic Quality Management System). Maintains secure storage and retrieval systems for both electronic and hardcopy records.
- Maintain high-quality technical documentation by reviewing, editing, releasing and archiving procedures, work instructions and forms following company's document change procedure.
- Responsible for formatting, proper spelling, organization, and clarity of text for any written documents submitted to Document Control.
- Manages physical inventory of documents control including documentation in the electronic database of documentation and outside storage.
- Maintains document traceability including revision history, approval records, and distribution logs.
- Trains and assists team members in the use of the document control system.
Requirements
- Prompts document review as required.
- Must have strong trouble shooting and problem-solving skills
Nice to have
- College degree or BS in Food Science, Quality Assurance, Regulatory Affairs, or related field preferred
Company info
- The Quality Document Control Specialist coordinates activities to ensure compliance with company's policies and procedures to meet GMP and regulatory guidelines.
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This listing is sourced directly from Byheart's careers page and normalized into a canonical job model.