(Sr) Specialist, QA Document Control (Temp)

Company: AbelZeta Inc
Location: Rockville
Posted on: February 20, 2026

Job Description:

Job Description Job Description AbelZeta Inc. is a clinical-stage biopharmaceutical company focused on leveraging our R&D capabilities to discover and develop T cell-based therapeutic products to treat cancer and inflammatory & immunological diseases. We are seeking a (Sr) Specialist, QA Document Control (Temp) to join our QA Compliance team. The role is responsible for managing and maintaining GxP documentation across multiple functional areas to ensure compliance with internal procedures, regulatory requirements, and industry best practices. This role plays a critical part in supporting quality systems, audits, and day-to-day document lifecycle management within a biopharmaceutical environment. Primary responsibilities Oversee the document lifecycle across all GxP functional groups to ensure adherence to internal procedures and applicable regulations and industry best practices. Maintain documentarchiveaccording to retention requirements. Maintain confidentiality around sensitive documentation. Administer electronic document management system, including permissions, access control, and issue resolution. Review and approve GxP documents in document management system to ensure compliance and accuracy of format,revisions, and metadata. Issue and reconcile controlled copies. Conduct document control-related training within the organization. Respond to documentation requests from internal and external stakeholders in a timely and professional manner according to the procedures. Monitor and report KPIs,including document status, and outstanding actions related to document control. Participate in documentation control related quality events as needed. Support internal and external audits by maintaining organized, accurate, and accessible documentation. Other Qualitytasks as needed. Essential Skills and Requirements Associate degree in science field or a similar discipline 2-5years ofhands-onexperience in the biopharmaceutical industry performing Document Control duties. Expertise in principles and practiceof current Good Manufacturing Practices (cGMPs). Strong knowledge of good documentation practices(GDP). Ability to manage multiple tasks, prioritize work, and escalate issues appropriately. Hands on experience with electronic document management system(s) in Document Control role. Proficiency with Microsoft Office Suite/Office 365 (e.g., Outlook, Teams, Word, Excel, PowerPoint, etc.) Preferred Qualifications Bachelor’s degree in a science field or a similar discipline. The ability to organize, prioritize, and deliver tasks with a sense of urgency under minimal supervision. Strongtechnical written skillsto author procedures. The ability to effectively build and maintain relationships with multiple departments in order to effectively solve problems. Strongability to analyze and interpret data. This is a temporary position, with one-year contract. You will be employed through a staffing agency

Keywords: AbelZeta Inc, Chantilly , (Sr) Specialist, QA Document Control (Temp), Science, Research & Development , Rockville, Virginia