A global biopharma company is seeking a Site Lead Auditor, Associate Director for its Dundalk facility.
This crucial role ensures compliance with c GMPs and Health Agency regulations.
Ideal candidates will have over 10 years of experience in the Biopharma industry, strong knowledge of c GMPs, 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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