Ensure that all review and release, manufacturing and packaging operations are appropriately compliant with applicable regulations (EMEA, FDA, DEA, MHRA, etc. where relevant). * Ensure Clinical Supply Quality processes directly support Technical Operations and goals and objectives. * Review and QA approval of deviations, change controls and complaints. * QA/compliance experience in manufacturing, facility operation, and quality systems. Areas of expertise should include compliance, quality assurance, quality control, validation, technical services, and an in-depth knowledge of at least one scientific discipline related to pharmaceutical sciences. * Must possess excellent interpersonal, verbal, and written communication skills at all levels internally and externally especially at
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