Job Description We are seeking a Manufacturing / Validation Engineer with a strong background in medical device manufacturing and process validation. This role is ideal for a technical writing workhorse who thrives on creating clear, detailed documentation while driving validation activities for new and existing equipment. You will play a critical role in ensuring compliance, supporting expansion projects, and maintaining robust manufacturing processes. 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/. Skills and Requirements • Experience in medical device manufacturing is required  • Experience in process validation planning, execution and reporting is required  • Strong technical writing skills related to process validation documentation as well as manufacturing process documentation (work instructions, standard operating procedures, etc.) is required Candidate to have 2-5 years of experience minimum