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One of our large Medical Device companies is actively looking for a Remote Technical Writer to join the Digital Transformation team. The Technical writer is primarily responsible for the development of new and revised Standard Operating Procedures (SOP), Work Instructions, & Computer System Validation (CSV) Test Scripts. The Goal of this project is to deploy new digital capabilities to enable automation of product release processes. Responsibilities include: Create new SOPs governing execution and support of deployed digital solutions Collaborate with site process owners and experts to revise existing procedures Manage change control process in client PLM system for all documentation Support training materials development and deployment Support draft of User Acceptance Test scripts Engage with project stakeholders to facilitate issue resolution Track progress and report task status Adhere to documentation quality standards This is a contract until end of June 2025, with high potential for extensions until end of year. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal. com. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ . 2-5 years of experience writing SOPs and Work Instructions Prior experience supporting CSV validation activities Highly proficient in Microsoft Office suite (Word, Excel, PowerPoint) Knowledge of medical device GxP requirements -Experience with UAT (User Acceptance Testing) Previous experience working with Windchill PLM