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QA/RA Documentation Specialist

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Onsite

QA/RA Documentation Specialist

Allied Medical LLC

QA/RA Documentation Specialist

Skills

Testing & QAInternal AuditCompliance

16 days ago

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Important information


Salary:

$47,840 – $52,000 / year

Location:

Earth City, MO, USA

Work mode:

Onsite

Published on:

12 October 2026

What they need


Description:

  • Owner of document control functions of change control by ensuring that records are readily available, properly defined, categorized, maintained, and implemented according to the document type.
  • Scanning files and dictating the organization of the file structure to establish a consistent place for the organization to pull records and procedures from. Support the shift to a paper-less system for record control.
  • Supporting regulatory with creating templates and providing relevant product documentation for submissions and registrations
  • Support the documentation and tracking of Nonconforming materials, dispositions and closures.
  • Training document coordination and management. Building tools (electronic and paper) to drive training capture, performance and materials for departments to utilize
  • Software Validation process ownership.Intake, recording, assisting software owners with validation expectations per the SOPs in place
  • Guide QMS sustaining activities through active completion of Standard Operation Procedure and Work Instruction expectations.
  • Coordinate the reporting/analysis of quality data and resolution of material and product quality issues
  • Improve process quality by making recommendations for change while working with relevant teams and departments to improve processes
  • Drive continuous improvements in all areas, focusing on key performance indicators
  • Support data collection and analysis for reporting on key performance indicators
  • Support site quality system activities to ensure compliance with international Regulations and Standards, including but not limited to 21 CFR 820, ISO 13485, EU MDR, and MDSAP requirements
  • Conduct internal audits, including closing out audit findings, create audit finding reports and determine proper corrective and preventative actions.

Requirements:

Required

  • 0-3 years’ experience in regulated industry
  • Experience with scanning, sorting and creating organized filing structures
  • Experience with MS Word, Excel, Powerpoint, Access and Adobe softwares
  • Excellent written and verbal communication skills.
  • Excellent organizational skills and detail oriented
  • Legally authorized to work in the United States.
  • Organization
  • Strong written and verbal skills
  • Collaboration skills
  • QA process skills
  • Computer knowledge and skill

Preferred

  • BA or BS degree in quality, engineering, or IT/Software discipline
  • Experience with quality quality processes and tools
  • Knowledge of safety requirements and legal standards
  • eQMS skills
  • Knowledge of ISO 13485, MDSAP, 21 CFR 820, MDR 2017/745
  • Quality Specialist (ASQ or similar Certifications)

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