Piper Companies
Piper Companies is seeking a Document Control Analyst to join a dynamic pharmaceutical team located in the Gaithersburg, MD area. This is an exciting opportunity to gain hands-on quality assurance experience. Responsibilities of the Document Control Analyst Include: •Assist authors and task owners with document revisions, deviation investigations, CAPAs, and change controls.•Support lower-level deviation investigations, including basic root cause analysis.•Ensure documents meet formatting and quality standards.•Manage document lifecycle activities in the Document Management System (DMS), including implementation, notifications, and controlled copy issuance/reconciliation.•Perform record management tasks such as issuing, reconciling, scanning, and archiving.•Provide technical support and troubleshooting for Document Control processes.•Identify and propose opportunities for process enhancements.•Support internal audits and regulatory inspections.•Participate in response teams to address audit observations and implement corrective actions. Qualifications of the Document Control Analyst Include: •Minimum requirement of a High School Diploma; Associate's or Bachelor's degree preferred.•1-3 years of direct experience in document control or quality systems in the life sciences industry.•GMP/GDP knowledge is required.•Experience with paper-based and/or electronic document control systems.•Familiarity with document management systems and regulatory requirements in pharma is a plus. Compensation of the Document Control Analyst Includes: •Pay range: $20.00 - $30.00 per hour, based on experience and education.•Comprehensive benefits: Cigna Medical, Dental, Vision, ADP 401k, PTO, Paid sick leave as required by lawThis job opens for applications on 9/3/2025. Applications for this job will be accepted for at least 30 days from the posting date.QA Document Control Analyst, biopharmaceutical, quality assurance, document control, GMP compliance, pharmaceutical QA jobs, biotech document control, regulatory documentation, SOP management, CAPAs, FDA regulations, QA analyst biotech, pharmaceutical quality systems, controlled documents, QA documentation, biotech careers, pharma document control, validation protocols, audit support, QA documentation analyst, pharmaceutical industry jobs, biotech quality assurance, document control coordinator, QA compliance specialist, pharmaceutical manufacturing QA, biotech regulatory affairs, entry level qa, entry level quality assurance #LI-CP1 #LI-ONSITE