Documentation Specialist-In Office

Join a Top leading company in the Medical Device industry!This Jobot Consulting Job is hosted by: Julibeth CanafaxAre you a fit? Easy Apply now by clicking the "Quick Apply" buttonand sending us your resume.Salary: $22 - $25 per hourA bit about us:Join a Top leading company in the Medical Device industry!Why join us?MedicalDentalVisionJob DetailsThe Quality Support Coordinator Provides administrative and operational support for quality‑related processes, including performance tracking, reporting, and coordination of internal and external feedback.Hours: 1st shift 8am-430pmDays: Monday-FridayJob Requirements:

• Ensure all documents meet regulatory requirements, quality standards, and internal procedures before release.
• Scan, organize, and maintain both physical and digital files, including archiving historical records for long‑term retention.
• Manage user access, permissions, and system integrity within internal document control or ERP systems.
• Schedule recurring and ad‑hoc meetings as requested by internal departments to support workflow needs.
• Review documents for formatting accuracy, compliance, and proper version control.
• Collaborate with cross‑functional teams to support document workflows, resolve discrepancies, and maintain consistency across documentation practices.
• Maintain record retention timelines and ensure documentation is accessible for internal and external audits.
• Process approved changes promptly, including updating information within internal ERP or document control systems.
• Maintain internal viewing or document repositories by uploading current versions and removing outdated revisions.

Qualifications

• Computer skills: Excel, Word, PowerPoint, Access, Outlook
• Familiarity with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP), as well as general regulatory expectations for controlled documents and records.
• Understanding of document control principles aligned with standards such as CFR 820.40 (Document Control) and ISO 13485 sections related to document and record management (e.g., 4.2.3, 4.2.4, 4.2.5) is preferred.
• Bilingual (English/Spanish) a plus

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