Biotech and Pharmaceutical, Change Control, Document Change Management, Document Control, Document Management, Documentation, Documentation Review, Legal, Manufacturing, Operational Support, Process Management, Quality Assurance, Quality Control, Quality Management, Standard Operating Procedures (SOP), Support Documentation, Technical Writing, Writing Skills
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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