QA Document Control Analyst

Piper Life Sciences is seeking a QA Analyst (Document Control) to join a biotechnology company in the Columbia, MD area. Responsibilities for the QA Analyst include: • Processing and managing the full life cycle of documents from initiation to release in the eDMS system • Ensuring adherence to regulatory requirements and current site practices in support of clinical and commercial manufacturing • Issuing batch records, worksheets, logbooks, and other requested documents to support QC, Manufacturing, and Quality Assurance • Scanning and physically filing documents and/or records to their designated locations • Maintaining the document archive rooms to ensure records are preserved, organized, structured, and accessible in a timely manner Qualifications for the QA Analyst include: • Bachelor's Degree in Science, Technical, or related degree is required • 2 years of experience in using an electronic document management system (eDMS) within a GMP regulated environment • Knowledge of the Microsoft suite (i.e. Word, Excel, Visio, PowerPoint, etc.) and Adobe is preferred Compensation for the QA Analyst includes: • Salary Range: approximately $28 - $32 hourly, commensurate with experience • Benefits: Medical, Dental, Vision, 401k Document control, archive, archival, archivist, doc control, qa, quality assurance, quality associate, quality specialist, quality assurance specialist, gmp, cgmp, gxp, mastercontrol, veeva vault, edms, document management system, pharma, biopharma, medical device, biotech, biotechnology, fda, quality systems, qms, eqms, clinical manufacturing, commercial manufacturing, novel pharmaceutical, novel drug, novel therapeutic LI-CP1 LI-ONSITE