Participate in the management of QA through active participation in QA forums and other meetings. * Proactively support the activities of Clinical supply for relevant manufacturing quality systems (deviation close out / Change management / complaints / quality improvement). * Management of Quality Complaints of IMP * Support the of Clinical Supply Quality in ensuring an acceptable outcome of all audits and inspections, especially those by government agencies, as they pertain to Process Support and Package Development practices (where relevant), equipment, and facilities. * QA/compliance experience in manufacturing, facility operation, and quality systems. * Must possess excellent interpersonal, verbal, and written communication skills at all levels internally and externally especially
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