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Kymanox

Associate Regulatory Technical Writer (FDA GMP)

Kymanox, Indianapolis, Indiana, us, 46262

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A life sciences professional services company is seeking an entry-level Associate Technical Writer to produce FDA-compliant documentation in a collaborative environment. You'll author and revise SOPs, protocols, and reports while working closely with subject-matter experts. This role offers a chance to learn within a dynamic team dedicated to improving patient outcomes and advancing your career in the life sciences sector. An ideal fit would have a relevant bachelor’s degree and excellent communication skills. #J-18808-Ljbffr