Technical writer

Summary

Authors and revises GMP documents.

Authoring new documents to support raw material testing including, but not limited to, specification authoring and Certificate of Analysis creation.

Revising existing documents as needed.

Managing the development of documents through the electronic document management system.

Assisting in the execution of Change Controls as needed.

Working with internal teams to obtain an in-depth understanding of QC processes and their documentation requirements.

Producing high-quality documents that meet applicable standards and are appropriate for their intended audience.

Writing easy to understand instructions where required.

Creating tutorials to help end-users train on a variety of activities.

Creating and maintaining documentation projects and timelines.

Providing excellence attention to detail when writing or revising documents.