A leading biopharma company in Sligo seeks a QA Validation Engineer for an initial 12-month contract. 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. Apply via email or contact Kellie for more details.
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