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

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