At Thorne, we work to deliver high-quality, science-backed solutions to empower individuals to take a proactive approach to their well-being. Each day begins with a mission to help others discover and achieve their best health. We count on our team members to challenge and push the boundaries to make that happen. At Thorne, you’ll be joining a team of more than 750 passionate individuals committed to our cause of providing superior health solutions at every age and life stage.

The Production Document Specialist I is responsible for drafting and revising controlled
manufacturing documentation in support of Production. This role contributes to the creation and revision of Standard Operating Procedures (SOPs), Work Instructions (WIs), GMP Forms, and related documentation within a regulated manufacturing environment. The position requires foundational technical document experience and a working knowledge of Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP).