GMP Technical Writer – Process Documentation

A leading biopharmaceutical company seeks a Technical Writer to transform complex technical processes into clear documentation. The role involves collaborating with MSAT engineers and ensuring Compliance with GMP standards. Candidates should possess strong technical writing skills, ideally with 0-3 years of relevant experience in a GMP environment. This position is based in Fishers, IN, and the company promotes a collaborative culture focused on quality outcomes.
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