Job Description Our large medical supply client looking to bring on a Quality Engineer at their Hartland, WI manufacturing plant. This facility manufactures a variety of products including medical devices, drug products, and cosmetics. Products include, but are not limited to - shampoo, syringes, canisters, swabs, tablets, pre-surgical products, and disinfectant wipes. The Quality Engineer must be comfortable with a varying day to day and being able to shift priorities. They will be looking at investigations (CAPAs, NCRs, deviations) and involved in validations. They may own a few different product lines and need to learn/understand the process, support the validations, and manage day-to-day issues that come up. This position requires hands-on ownership of product lines. We are ideally looking for someone with a quality engineering background at a GMP manufacturing site who has experience with technical writing and non-conformance, CAPAS, deviations, and/or risk management activities. 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 5+ years experience of experience in quality engineering at a GMP manufacturing site  Background in a regulated industry (pharma or medical devices)  Experience working with non-conformance, CAPAS, deviations, and/or risk management activities  Technical writing experience  Knowledge of SAP  Strong Microsoft Office skills (Excel, Word, Outlook, etc.)  Strong communication and interpersonal skills collaborating with different departments/divisions  Comfortable working in a manufacturing environment 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.