
Pharmaceutical manufacturing professional with 7+ years of experience in GMP-regulated environments supporting sterile drug product and vaccine manufacturing operations. Proven expertise in aseptic processing, automated visual inspection systems, lyophilization, vial washing, and osmolality testing. Strong background in maintaining compliance with Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and standard operating procedures (SOPs). Recognized for maintaining high quality standards, supporting efficient production processes, and ensuring regulatory compliance in controlled manufacturing environments.
This course is for individuals who will be performing instructor-led or OJT (on-the-job) training.