This Technical Writer position in Vandalia, Ohio involves managing documentation related to commercial production, technical transfers, and R&D support. The role includes drafting, revising, and maintaining batch records, SOPs, protocols, and reports, as well as supporting quality systems like CAPA and Change Control. The candidate will act as an SME for electronic documentation, lead SOP reviews, assist with validation reports, and contribute to scientific publications and technical presentations. Strong organizational skills, attention to detail, and experience in a regulated environment are essential. The role offers opportunities for professional growth within a collaborative, fast-paced company committed to continuous improvement and compliance with FDA and cGMP standards. The position requires 2-5 years of related experience or a relevant degree, proficiency in Microsoft Office, and excellent communication skills.