Our client, a Global Medical Device Manufacturer, has an immediate opening for a Quality Assurance Specialist for a 9 Month+ contract. You will have the opportunity to work with other like-minded, self-directed and detail oriented Top Talents in an extremely collaborative and professional environment. The contractor in this role will support the implementation and validation of replacement Product Lifecycle Management (PLM) system, including data and records migration from the legacy PLM platform and seamless integration with the Manufacturing Execution System (MES). This is a project-based role focused on computer system validation (CSV) including documenting user requirements, supporting PLM configuration, and developing User Acceptance Testing (UAT) and GxP system validation deliverables. The role plays a critical part in ensuring compliant, high-quality system adoption and a successful go-live. 1st Shift (CST) - Can be remote/hybrid
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