**Document Control Specialist II**

Quality Assurance

Vista, California, US

+ Added - 01/06/2026
**Document Control Specialist II**

**Position Summary**

A growing manufacturer of drug substances is seeking a Document Control Specialist II to join its QA team.

In this role you will help ensure that drug substances are produced in compliance with FDA and international regulatory requirements across research, pre-clinical, clinical, and commercial stages. The position centers on the review and processing of GMP documentation, day-to-day quality oversight, guidance to other functions on cGMP matters, and support for customer and regulatory audits. You will also help maintain GMP records and the supporting electronic quality systems.

**Location** : Onsite in Vista, CA | **Hours** : M-F 8-5 | **Type** : 1-year contract | **Compensation** : $39-$52/hour

**What You Will Do**

**Core Responsibilities**

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