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ROLE SUMMARY Reporting to the Senior Manager, Validation & Qualification, the Manager, Process Performance Qualifications leads a team of validation engineers responsible for Process Qualification, Cleaning Validation, and Continued Process Verification (CPV) activities supporting sterile injectable manufacturing operations. The
ROLE SUMMARY Accountable for supporting activities involved in the design, development, transfer, and lifecycle management of manufacturing processes for sterile pharmaceutical products. The candidate selected will be a subject matter expert for PC1 Lifecycle & Lyophilization.
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