- Florence, South Carolina, United States
- 3–5 years
Provide quality oversight and support in manufacturing operations to ensure GMP compliance and continuous improvement.
Responsibilities
- Review and approve GMP documentation, batch records, and quality records
- Investigate quality events and root cause analysis
- Maintain quality management system documentation
- Support quality investigations and regulatory inspections
- Assist in writing and revising SOPs and procedures
Requirements
- High School diploma
- Bachelor's degree
- Nice to have: ISO auditor
- Nice to have: Six Sigma
- Nice to have: Bachelor's degree in Chemistry, Biology, Engineering, Life Sciences