Document Control Specialist

Document Control Specialist - Quality (CR/511742) Bedford, Massachusetts Salary: USD30 - USD34 per hour A biotech organization located in Bedford, MA is seeking a Document Control Specialist, Quality, to support document management operations within a quality environment. This role focuses on processing and maintaining GxP documents throughout their lifecycle, with an emphasis on controlled issuance, reconciliation, and archival. About the Opportunity: Schedule: Monday to Friday Setting: Onsite Responsibilities: Follow the Standard Operating Procedures (SOPs), work instructions, and other administrative practices Organize and manage a high volume of documentation for electronic and paper-based archival Assist with filing, retrieval, retention, and archival of documents and records Support the issuance of controlled documents and related document reconciliation activities Provide Document Control support before, during, and after audits and inspections Qualifications: 1-4 years of Quality experience in the Pharma, Biotech, or related Life Sciences industry Bachelor’s Degree in Science, Engineering, or related discipline Experience in Document Control and Electronic Document Management systems Strong attention to detail and organizational skills Ability to work independently, prioritize tasks, and manage multiple assignments simultaneously. Knowledge of GDP and cGMP principles Proficiency in Microsoft Excel, Word, and PowerPoint High ethical standards, good judgment, and professionalism Desired Skills: Experience documenting processes and supporting continuous improvement efforts Exposure to audit and inspection support in a regulated environment CV / Resume: supported file types: .doc .docx .odt .pdf .rtf .txt #J-18808-Ljbffr