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 Writer

• Author, revise, and maintain SOPs, methods, and controlled QC documents
• Manage document control processes including routing, approvals, and implementation
• Support change control activities and periodic document reviews
• Coordinate updates based on feedback from QC analysts and stakeholders
• Ensure documentation complies with cGMP/GDP standards
• Track and manage documentation within internal systems
  
  

Qualifications Of The QC Document Control Writer

• 2 years of experience in document control, technical writing, or quality documentation
• Strong knowledge of GMP/GDP and regulated environments
• Experience with SOP writing, change control, and document management systems
• Background in pharmaceutical, biotech, or manufacturing environments preferred
• QA or QC experience is a plus
  
  

Compensation For The QC Document Control Writer

• Pay Rate Commensurate to Experience
• Long-term Contract Opportunity
• Comprehensive Benefits: Medical, Dental, Vision, 401K, Sick Leave (as required by law), and Paid Holidays
  
  

Application Period: This position opens for applications on 6/1/2026 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