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On-site validation specialist – gmp

Stamullin
PCI TRGR Penn Pharmaceutical Services Ltd
Validation specialist
Posted: 11 December
Offer description

A leading pharmaceutical company in Stamullen is seeking a Validation Specialist for a permanent role.
The position involves ensuring compliance with industry standards, executing validation tasks for processes and equipment, and generating necessary documentation.
Candidates should possess a degree in Quality/Validation and 2-5 years' experience in a regulated environment.
This on-site role requires strong problem-solving skills, adaptability, and proficiency in Microsoft Office.
Join us to support the delivery of life-changing therapies to patients.
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