Job Overview
Start Date:
ASAP
Location:
Galway, Ireland (full time onsite)
Duration:
6 months + extensions
Key Responsibilities
Review, edit, and revise existing QMS documentation to align with current standards and best practices.
Translate complex processes into clear, user-friendly SOPs and workflows.
Ensure documentation meets compliance and validation requirements.
Collaborate with subject matter experts (SMEs), quality teams, and process owners to gather information and confirm accuracy.
Standardize documentation formats and ensure version control within the QMS.
Support the design and implementation of new workflows based on business needs.
Provide recommendations to improve clarity, usability, and compliance of controlled documents.
Contact Information
If you are interested, please submit your CV or send it to
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