Job Description One of our large pharmaceutical clients is actively hiring for a Technical Writer for a new manufacturing building, that supports Live Virus Vaccine Manufacturing Filling. The Technical Writer will be responsible for completing the revision of 150 SOP documents for formatting and consistency. You will be working with the Operations, Manufacturing and Engineering subject matter experts to review the SOPs, understand what needs to be updated, complete redlining, formatting & grammatical edits, & then the Technical Writer will be using MS Word to make the edits and submit through the document revision process. Examples of formatting you will be required to review are alignment of bulleting, pictures, making sure pictures are readable, font & font sizes are consistent, etc. You will be trained in their internal document management system process. This is a fully remote position, working part-time around 20 hours per week. We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, 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 Human Resources Request Form (https://airtable.com/app21VjYyxLDIX0ez/shrOg4IQS1J6dRiMo) . The EEOC "Know Your Rights" Poster is available here (https://www.eeoc.gov/sites/default/files/2023-06/22-088\_EEOC\_KnowYourRights6.12ScreenRdr.pdf) . 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/ . Skills and Requirements - 3-5+ years of Technical Writing experience within a GMP manufacturing environment - Experience reviewing, editing, and improving SOPs in MS Word - Previous biotech/pharmaceutical industry experience Self-starter with the ability to manage individual project timelines with minimal oversight Pharma Manufacturing Technical Writing Experience working in KNEAT null 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 employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to 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 oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to HR@insightglobal.com.