Responsibilities:
Requirements:
• Bachelor’s degree in a scientific or technical field (Biology, Chemistry, Engineering, etc.)
• 3–6 years of experience in pharmaceutical manufacturing, QA, or aseptic operations
• Hands-on experience providing QA oversight on the manufacturing floor
• Experience with line clearances, batch record review, and GMP documentation
• Familiarity with deviations, root cause analysis, and CAPA
• Strong understanding of cGMP and regulatory standards (FDA, EMA, etc.)
In-Process Quality Technician • Raleigh, NC, US
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