QC Document Control Writer

Piper Companies is seeking a QC Document Control Writer to support a global, industry-leading pharmaceutical organization in Athens, GA. The QC Document Control Writer will be responsible for managing and updating quality documentation to support QC operations in a regulated environment.Responsibilities Of QC Document Control WriterAuthor, revise, and maintain SOPs, methods, and controlled QC documentsManage document control processes including routing, approvals, and implementationSupport change control activities and periodic document reviewsCoordinate updates based on feedback from QC analysts and stakeholdersEnsure documentation complies with cGMP/GDP standardsTrack and manage documentation within internal systemsQualifications Of The QC Document Control Writer2+ years of experience in document control, technical writing, or quality documentationStrong knowledge of GMP/GDP and regulated environmentsExperience with SOP writing, change control, and document management systemsBackground in pharmaceutical, biotech, or manufacturing environments preferredQA or QC experience is a plusCompensation For The QC Document Control WriterPay Rate Commensurate to Experience Long-term Contract Opportunity Comprehensive Benefits: Medical, Dental, Vision, 401K, Sick Leave (as required by law), and Paid HolidaysApplication Period: This position opens for applications on 4/27/2026 and will remain open for a minimum of 30 days from the posting date.Keywords: Technical Writer, Documentation Specialist, Document Control, SOP, cGMP, GDP, Quality Assurance, pharmaceutical