One of our large pharmaceutical clients is looking to hire a Quality Excellence Associate to join their growing team. This individual will be leading Continuous Improvement site initiatives that improve safety, improve overall quality of execution, increase process efficiencies, and reduce cycle time and cost. Main responsibilities will include, but are not limited to:
- Pull and analyze data from quality groups to prepare analyses and presentations, streamline processes, and develop insights for team meetings.
- Format all reporting/data sets for meeting agenda, prepare presentations, and upload CRB Minutes in EDMS.
- Combine weekly data to analyze and send out for review. Format all reporting for presentation and upload QSMR report into Truvault.
- Investigate Trend report to track deliverables, format report and upload in EDMS.
- Support development of Quality Risk Management Framework.
- Support Quality Systems Tasks e.g., Site Master File maintenance, Gap Assessments, Quality Agreements

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