Quality Systems Specialist - Document Control

Stryker

Belfast, United Kingdom
Hybrid
Document control system administration
Compliance with fda regulations
Version control of quality documents
The Document Control Specialist is responsible for managing, organizing, and maintaining controlled documents to ensure compliance with FDA regulations, ISO 13485, and company quality management system requirements

Job Summary

  • The Document Control Specialist is responsible for managing, organizing, and maintaining controlled documents to ensure compliance with FDA regulations, ISO 13485, and company quality management system requirements.
  • This role supports cross-functional teams by ensuring accurate documentation, proper version control, and timely distribution of quality and regulatory documents.
  • The position involves coordinating internal and external audits and providing documentation to ensure records are complete and accurate.

Matching Summary

The Document Control Specialist is responsible for managing, organizing, and maintaining controlled documents to ensure compliance with FDA regulations, ISO 13485, and company quality management system requirements.

Skills & Requirements

Must-have

  • Document control system administration
  • Compliance with FDA regulations
  • Version control of quality documents

Nice-to-have

  • Strong interpersonal skills
  • Basic understanding of medical device regulations
  • Experience in cross-functional teams

Key Requirements

  • Level 6 qualification
  • 0-2 years experience

Work Rights

Not specified

Tailored Resume

Cover Letter