Quality Assurance Specialist will work in a cGMP regulated pharmaceutical company. Daily activities may include auditing, document review, investigations, writing of reports and quality system development and implementation in both an individual and team setting. Direct Reporting: The Quality Assurance Specialist will report directly to the Quality Assurance Manager Role: To assure the company remains compliant with FDA regulations and internal procedures and to support activities consistent with company objectives. Responsibilities: Duties will be delegated by the Quality Assurance Manager and may include internal auditing, conducting investigations, creating and reviewing validation documents, creation and revision of procedures and batch record...read more

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