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Data Validation Specialist
3 weeks ago
Job Overview
We are seeking a QA CSV Specialist to join our team in Limerick. This is an exciting opportunity to work with a leading global pharmaceutical client.
The successful candidate will be responsible for ensuring Computer System Quality across all site systems, reviewing and approving Validation documentation, providing training on CSQ, and supporting associated Computer System maintenance activities.
- Key Responsibilities:
- Ensure Computer System Quality across all site systems.
- Responsible for Validation documentation review and approval.
- Provide training on CSQ.
- Support associated Computer System maintenance activities.
Requirements
- Essential Skills:
- A minimum of several years’ experience within a relevant QA CSV position within a GMP environment.
- Major Capex project experience is highly desirable.
- Experience implementing Computer System Quality guidelines and ensuring regulatory and organisational compliance.
- Excellent communication and teamworking skills.
About the Role
This is a 6-month initial contract opportunity that offers the chance to gain valuable experience working with a leading global pharmaceutical client. If you have the necessary skills and qualifications, we would like to hear from you.
