**Work Schedule**

First Shift (Days)

**Environmental Conditions**

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

**Job Description**

Join us a a QA Auditor I - And play a crucial role in ensuring compliance and excellence in our clinical auditing processes.

**What You’ll Do:**

• Support IQA/SQA group as responsible for specification revisions of Commodities (CMS) and Raw Materials (RMS) specification documents. Note – this individual is not expected to be a subject matter expert. Expected to manage the revision process. See below for further info.
• Work as a liaison between the operating groups and the Document Control group to facilitate the identification, writing, reviewing, and approval of all documents to support a given project.
• Route and monitor document change control packages, managing a revision through effectiveness. Manage timelines and work to a need-by date to support ma...