A leading pharmaceutical company in Dundalk is seeking a dedicated Site Lead Auditor, Associate Director. This position plays a crucial role in ensuring process compliance with regulations and cGMPs. Ideal candidates will have a bachelor's degree and over 10 years of experience in the Biopharma/Pharma industry. Responsibilities include developing the internal audit program and leading audits while advocating for continual improvement in quality management systems. The role is part of a hybrid model promoting flexible working arrangements.
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