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 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
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