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Process Transfer and Validation Coordinator
Ref No.: 18-19465
Location: Andover, Massachusetts
Process Transfer and Validation Coordinator
Andover, MA
1 Year



2 years of experience in biopharmaceutical production, testing, or process development; 1 year of experience in document management system; 1 year of experience in laboratory information management system

The Process Transfer and Validation Coordinator is responsible for coordinating and supporting activities related to the transfer and validation of biologics drug substance manufacturing process to the Andover manufacturing facilities. Primarily responsibilities include:

1. Coordinating and scheduling technology transfer, validation, and production related activities
2. Management of the identification, collection, distribution, analysis, and result compilation of process samples associated with validation and production activities
3. Authoring of technical protocols, reports, and regulatory submissions
4. Compilation and verification of process data used in technical reports and regulatory submissions
5. Maintenance of collaboration and productivity software tools used to facilitate technology transfer, validation, and production planning
6. Providing administrative support for activities associated with technology transfer, validation, and production planning