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QA Validation Engineer - cGMP & Regulatory Focus
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- Ireland
- Ireland
À propos
The experience expected from applicants, as well as additional skills and qualifications needed for this job are listed below.
The successful candidate will coordinate the site validation program, ensuring compliance with cGMP standards and regulatory requirements.
Responsibilities include managing validation processes, generating protocols, and participating in quality improvement initiatives.
Ideal for candidates with engineering or scientific qualifications and over 3 years in the med device industry. xcfaprz
Apply via email or contact Kellie for more details.
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Compétences linguistiques
- English
Avis aux utilisateurs
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