A global biopharma solutions provider is seeking a Validation Specialist to implement and execute validation tasks related to Process, Facility, and Equipment development.
The ideal candidate should have 2-5 years of relevant experience in a GMP environment and possess a degree in Quality or Validation.
The position is full-time, Monday to Friday, and located on-site in Stamullen, County Meath, Ireland.
Join the team to contribute to successful project deliveries and ensure compliance with regulatory standards.
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