A global biopharma company is seeking a Site Lead Auditor, Associate Director for its Dundalk facility. This crucial role ensures compliance with cGMPs and Health Agency regulations. Ideal candidates will have over 10 years of experience in the Biopharma industry, strong knowledge of cGMPs, and excellent communication skills. You will lead audits and advocate for continuous improvement. This position offers a hybrid work model and the opportunity to make a significant impact in quality assurance.
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