TECHNICAL WRITER, REMOTE | WORK FROM ANYWHERE

This role will provide non-testing support to the QC Analytical department for product life cycle management and technology transfer activities. This scope includes coordination of generating validation and transfer documents to support monoclonal antibody product life cycle and transfer between Pfizer sites. The technical skills within the scope will require an understanding of the scientific principles of test methods, data analysis, and cGMP requirements. The candidate will be responsible for facilitating lifecycle management and tech transfer through collaboration with laboratory subject matter experts (SMEs) and analysts.

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