ARTO
Quality Specialist
2 months ago
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Important information
Contract type:
Freelance / Contract
Location:
Dublin, Ireland
Work mode:
Onsite
Published on:
12 August 2026
What they need
❗ Documentation Quality Specialist | Dublin | Contract ❗
We are looking for an experienced Documentation Quality Specialist to support a global pharmaceutical organisation with the management, governance and continuous improvement of its global QMS documentation processes .
This is an excellent opportunity for a Quality professional with strong experience across GxP documentation, Document Control and Quality Management Systems , working with stakeholders across an international organisation.
📍 Location: Dublin, Ireland
📋 Contract: Consultant / Contract
Key Responsibilities
Coordinate and maintain the global QMS documentation process , ensuring consistent and compliant document management across the organisation.
Support the full documentation lifecycle , including document creation, revision, review, approval, implementation and archiving.
Ensure documentation meets applicable GxP, Quality and Data Integrity requirements .
Review and support the development of high-quality SOPs, procedures, policies and other controlled Quality documentation .
Provide training and guidance to stakeholders on documentation standards, processes and best practices.
Prepare, monitor and report documentation KPIs and metrics , identifying areas requiring improvement.
Coordinate and contribute to documentation forums with relevant Quality and business stakeholders.
Drive continuous improvement and harmonisation of documentation processes across the global organisation.
Work cross-functionally with Quality and other departments to promote consistent documentation practices.
🔍 What we're looking for:
- 5+ years ' experience in GxP , within the pharmaceutical or biotechnology industry
- Strong technical documentation writing skills
🔎 Particularly interested in consultants with strong QMS + Document Control + GxP Documentation experience.
If you have experience managing and improving controlled Quality documentation processes within a pharmaceutical or biotech environment , please apply or get in touch directly to discuss the assignment.
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