Piper Companies
Overview
Piper Companies
is seeking a detail-oriented
Quality Document Control Analyst
to join our dynamic team in a fast-paced biopharmaceutical environment out of
Gaithersburg, MD . This role is critical to ensuring compliance with regulatory standards by managing controlled documents, supporting audits, and driving continuous improvement in documentation practices. Responsibilities
Manage the lifecycle of controlled documents including SOPs, batch records, protocols, and training materials Review, revise, and format documents to ensure alignment with regulatory and internal standards Support deviation investigations and CAPA documentation by compiling evidence and tracking corrective actions Maintain document control systems and ensure accurate indexing, versioning, and archival of records Assist in preparation for internal and external audits by ensuring documentation readiness and compliance Qualifications
1+ years of experience in document control and/or Quality Assurance (QA) within a GMP-regulated biopharmaceutical or biotechnology environment Strong understanding of cGMP, GDP and regulatory compliance requirements Experience with batch records, controlled documents, audit reporting and quality documentation practices Proficiency in document management systems, QMS, Microsoft Office Suite Excellent attention to detail, organizational and ability to manage multiple priorities Very strong communication skills Bachelors degree in science related field (Biology, Biotechnology, Biological Sciences, Chemistry, Molecular & Cell Biology, etc.) Compensation
Salary: $50,000 65,000 annually, commensurate with experience Comprehensive Benefits: Medical, Dental, Vision, 401k, Sick leave as required by law, PTO (Paid Time Off) This job opens for applications on 09/05/2025. Applications for this job will be accepted for at least 30 days from the posting date. Keywords
QA, quality assurance, document control, document archival, archival, document control analyst, doc control, document control specialist, biotechnology, biopharmaceutical, pharmaceutical, cell therapy, document management system, DMS, QMS, quality management system, veeva, GMP, good manufacturing practice, GDP, good document practice, batch record, audit, regulatory audit, regulatory, regulatory compliance, cGMP, current good manufacturing practice, manufacturing associate, upstream, downstream, all stream, controlled documents, SOP, standard operating procedure, laboratory, indexing, CAPA, CAPA documentation, CAPA investigations, deviations #LI-BN1 #LI-ONSITE #J-18808-Ljbffr
Piper Companies
is seeking a detail-oriented
Quality Document Control Analyst
to join our dynamic team in a fast-paced biopharmaceutical environment out of
Gaithersburg, MD . This role is critical to ensuring compliance with regulatory standards by managing controlled documents, supporting audits, and driving continuous improvement in documentation practices. Responsibilities
Manage the lifecycle of controlled documents including SOPs, batch records, protocols, and training materials Review, revise, and format documents to ensure alignment with regulatory and internal standards Support deviation investigations and CAPA documentation by compiling evidence and tracking corrective actions Maintain document control systems and ensure accurate indexing, versioning, and archival of records Assist in preparation for internal and external audits by ensuring documentation readiness and compliance Qualifications
1+ years of experience in document control and/or Quality Assurance (QA) within a GMP-regulated biopharmaceutical or biotechnology environment Strong understanding of cGMP, GDP and regulatory compliance requirements Experience with batch records, controlled documents, audit reporting and quality documentation practices Proficiency in document management systems, QMS, Microsoft Office Suite Excellent attention to detail, organizational and ability to manage multiple priorities Very strong communication skills Bachelors degree in science related field (Biology, Biotechnology, Biological Sciences, Chemistry, Molecular & Cell Biology, etc.) Compensation
Salary: $50,000 65,000 annually, commensurate with experience Comprehensive Benefits: Medical, Dental, Vision, 401k, Sick leave as required by law, PTO (Paid Time Off) This job opens for applications on 09/05/2025. Applications for this job will be accepted for at least 30 days from the posting date. Keywords
QA, quality assurance, document control, document archival, archival, document control analyst, doc control, document control specialist, biotechnology, biopharmaceutical, pharmaceutical, cell therapy, document management system, DMS, QMS, quality management system, veeva, GMP, good manufacturing practice, GDP, good document practice, batch record, audit, regulatory audit, regulatory, regulatory compliance, cGMP, current good manufacturing practice, manufacturing associate, upstream, downstream, all stream, controlled documents, SOP, standard operating procedure, laboratory, indexing, CAPA, CAPA documentation, CAPA investigations, deviations #LI-BN1 #LI-ONSITE #J-18808-Ljbffr