FDA-Regulated Technical Writer — Life Sciences Documentation

A leading life sciences consulting firm is seeking an experienced Technical Writer to produce FDA-compliant documentation in a cGMP environment. The ideal candidate will have at least five years of experience in technical writing within regulated environments, including direct involvement in authoring SOPs, protocols, work instructions, and reports. This role requires strong interpersonal skills and the ability to collaborate with subject matter experts across multiple disciplines.

Join a dynamic team committed to improving lives through innovative solutions.
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