Job Description

Key Responsibilities include:
• Build and maintain technical GMP documents and product stability studies
• Review, verify, report, and archive GMP data for clinical and commercial products
• Apply keen attention to detail to conduct data review and reports
• Execute transactions in relevant GMP computer-based systems (change control, LIMS, etc.)
• Adeptly manage time-sensitive activities independently


Requirements

Basic Qualifications
• Doctorate degree, or
• Master’s degree & 3 years of Quality, Operations, Scientific, or Manufacturing experience, or
• Bachelor’s degree & 5 years of Quality, Operations, Scientific, or Manufacturing experience
Preferred Qualifications