QA Final Inspector

At DuPont, our purpose is to empower the world with essential innovations to thrive. We work on things that matter. Whether it’s providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the world’s most talented people are choosing to work at DuPont. Why Join Us | DuPont CareersDuPont’s Healthcare Industries Material Site (HIMS) is currently seeking a Quality Assurance Final Inspector at our site in Hemlock, MI.This position is a Document Center Specialist in support of our Quality Assurance team in managing critical production and raw material documentation.In this role you will ensure the accuracy, completeness, and compliance of batch records and quality documentation that support safe, reliable, and compliant manufacturing. The ideal candidate is highly organized, detail‑focused, and comfortable working in a fast‑paced environment with cross‑functional interaction.Key essentials of this role/what you’ll do:Documentation & Batch Record ManagementReview, verify, and approve production batch records to ensure compliance with internal procedures and regulatory requirements.Maintain accurate documentation across QA systems, including SAP, FastTrack, and SharePoint.Investigate and resolve documentation discrepancies by working directly with Quality, Production, and Laboratory personnel.Quality Systems & Data IntegritySupport the lifecycle of documentation, including sorting, organizing, scanning, filing, and archival of quality records.Execute routine quality tasks such as reviewing inspection lots, processing Certificates of Analysis (COAs), and managing DOM (Date of Manufacture) verification requests.Track and report documentation errors and monthly approval metrics used for quality performance reporting.Compliance & Continuous ImprovementAssist with validation document processing, ensuring accuracy and proper control of protocols and reports.Participate in annual record retention and destruction activities in alignment with corporate policies.Support process improvements that enhance document flow, accuracy, and efficiency within the Quality organization.Job QualificationsRequired QualificationsHigh school diploma or equivalent.Minimum 1 year experience in document control, batch record review, or laboratory/quality supportStrong attention to detail and accuracy when reviewing documentation.Proficiency with Microsoft Office tools (Word, Excel, Outlook).Ability to manage priorities in a regulated, deadline‑driven environment.Effective written and verbal communication skills.Preferred QualificationsExperience in GMP, ISO, or other regulated manufacturing environments.Familiarity with SAP, FastTrack, or electronic document management systems.Key CompetenciesStrong organizational skills and time‑management disciplineData integrity and compliance mindsetProblem‑solving and cross‑functional collaborationAbility to work independently with minimal supervisionWork EnvironmentOffice/Document Center setting with routine handling of physical documentation.Occasional lifting/movement of document storage boxes.Frequent interaction with Production, QA, and Laboratory teams.Join our Talent Community to stay connected with us!DuPont is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information.DuPont offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page.