Piper Companies is currently looking for a QA Document Control Manager in the Elkridge, MD area to work a fully onsite role. This QA Document Control Manager will join a global life sciences organization focused on the research, development, manufacturing, and commercialization of regulated healthcare products. Responsibilities for the

QA Document Control Manager:

Oversees document control activities to ensure regulatory and cGMP compliance. Administers the EDMS, including document workflows, approvals, and change controls. Reviews and maintains quality documentation, SOPs, and training records. Partners with cross-functional teams to support compliance and process improvements. Supports audits, inspections, and quality reporting activities. Qualifications for the

QA Document Control Manager:

Bachelor's degree in a relevant area or equivalent work experience Experience in a FDA regulated environment 8+ years' experience in a GMP environment Knowledge of cGMP and other regulatory requirements applicable to industry Compensation for the

QA Document Control Manager:

Hourly Rate:

$46-48/hr based on professional experience

Comprehensive Benefits:

Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and

Holidays Keywords:

Quality Assurance, QA, Quality Management System, c

GMP, GMP

Compliance, Regulatory Compliance, FDA Regulations, Quality Systems, Change Control, Risk Assessment, Manager, Management, Quality Documentation, Document Control, Document Management, Data, Document Review, Staff Management, Project Coordination, Workflow Optimization, Development, Quality Metrics, Pharma, Pharmaceutical Manufacturing #LI-EM1 #LI-ONSITE