Job Description

QA Specialist

Dublin, Ireland (Onsite)

Contract: 12 months 

Rate: €33/hr

Join us as a QA Specialist in Dublin and make a global impact in pharmaceutical quality. Work independently and as part of a cross-functional team to ensure excellence across supply operations. Strong communication, time management, and multitasking skills are essential to succeed in this fast-paced role.

Key Responsibilities

• Compile Qualified Person batch release dossiers
  
  
• Support Packaging and Labelling activities at EU Central Warehouse (EUWH)
  
  
• Provide QA support for the Use Date Extension process
  
  
• Deliver QA guidance and training (GMP/GDP) for CSO Regional Logistics
  
  
• Investigate non-conformances and quality incidents; document and track deviations, investigations, and CAPAs in the Quality Management System
  
  
• Author, maintain, and update ISR-related Quality Agreements
  
  
• Prepare release dossiers for ISRs
  
  
• Draft and review procedural documents as requested by supervisor
  
  
• Support the preparation of training materials
  
  
• Contribute to improving and maintaining the CSCQ Quality Management System
  
  
• Prepare and approve supply chain flow maps and product specification files
  
  
• Author, review, and approve QA-related procedures
  
  
• Generate or update Quality Agreements as required
  
  

Note: Responsibilities listed are a summary; additional tasks may be assigned as needed.

Requirements:

• BSc in Science or related discipline; pharma/QA experience preferred
  
  
• Solid understanding of cGMP requirements and compliance
  
  
• Strong communication, organizational, and multi-tasking skills
  
  
• Ability to work independently and collaboratively across teams
  
  
• Open to travel as needed