Job Summary
A prominent pharmaceutical company in Ireland is seeking a skilled CSV specialist to support validation activities for GMP-regulated systems.
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Key Responsibilities:
* Support validation activities across manufacturing, packaging, and laboratory environments.
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To succeed in this role, you will need:
1. a strong understanding of industry regulations,
2. a proven track record of experience in Computer System Validation (4-7 years), and
The ideal candidate will be able to collaborate effectively with cross-functional teams and contribute significantly towards ensuring compliance.
This role offers the opportunity to apply your knowledge and skills in an innovative environment where you can grow professionally.,