Position: Technical Writer- GMP Manufacturing Documentation

Location: Houston, TX (100% On-Site)

Length: 6 Month Contract

Please no agencies. Direct employees currently authorized to work in the United States – no sponsorship available

Job Description:

We are seeking an experienced Technical Writer to support GMP manufacturing operations within a pharmaceutical environment. This individual will play a key role in developing, updating, and managing critical GMP documentation during an active phase of a manufacturing project. The position requires close collaboration with cross-functional teams and will be fully onsite due to the critical path nature of the work.

Essential Duties and Responsibilities:

• Author, revise, and maintain GMP documentation including:
• Standard Operati...