

Detail-oriented Pharmaceutical Engineering graduate with hands-on experience in GMP-regulated environments, encompassing Process Engineering, R&D, and QA/QC functions. Skilled in cleanroom practices and SOP documentation, supporting production in medicine and supplement facilities. Committed to upholding compliance and quality standards, aiming to enhance sterile compounding and production operations in a regulated pharmaceutical facility.
• Provided education on nutritional supplement ingredients and product quality standards
• Interpreted formulation information and regulatory guidelines for customers
• Ensured compliance with approved product claims and ethical promotion practices
• Assisted in formulation trials and experimental data collection
• Conducted data analysis and prepared technical reports for internal review
• Supported documentation processes to ensure adherence to Good Manufacturing Practice (GMP)
• Collaborated with QA/QC teams during product testing and evaluation
GMP compliance & regulatory awareness
Cleanroom & aseptic process principles
SOP development & documentation control
Batch record support
Process flow & P&ID interpretation
QA/QC collaboration
Root cause analysis
Utilities systems support
Continuous improvement (5S exposure)
Strong communication & teamwork