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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.
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
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