CARMEN MASSO
CONTACT
Philadelphia, Pa.*****
******.*******@*****.***
SUMMARY
Pharmaceutical manufacturing and packing technician with over 20 years of experience in FDA-regulated manufacturing environments. Extensive experience supporting production in various areas. Proven ability to operate manufacturing equipment perform line clearances, complete batch records and maintain strict adherence to cGMP and SOP requirements.
EDUCATION
Pharmacy License
Pharmacy Technician Certification
Brian University
Pending
GED
Carolina, Puerto Rico
9/2000
RELEVANT EXPERIENCE
Pharmerica Production Associate Dec 2025 – Present
• Process medication orders.
• Assisted in the preparation and compounding of pharmaceutical products.
• Managed inventory levels and maintained detailed production records.
• Perform computer-based data entry and recordkeeping
• Adhered to (cGMP) and (SOPs) to maintain regulatory compliance. Polaris Pharmacy Production Associate Nov 2024 - Dec 2025
• Filled medication orders accurately and efficiently.
• Assisted with pharmaceutical compounding operations.
• Maintained inventory and production documentation.
• Performed computer-based data entry and recordkeeping
• Maintained compliance with cGMP regulations and SOPs. Hikma Pharmaceutical Manufacturing Technician Aug 2024 – Nov 2024
• Perform manufacturing operations in a sterile pharmaceutical environment.
• Follow aseptic gowning and contamination-control procedures.
• Monitor blend tanks, temperatures, and production processes.
• Complete manufacturing documentation and production calculations.
• Stage materials and support production readiness. AstraZeneca (Arotek) Packaging Technician Feb 2024 - Aug 2025
• Operated pharmaceutical packaging equipment and production lines.
• Conducted line clearance and changeover activities.
• Maintained compliance with cGMP regulations and SOPs.
• Performed equipment setup, cleaning, assembly, and disassembly.
• Maintained cold chain requirements during packaging operations.
• Calibrated scales and completed production documentation. Bristol Myers Squibb Manufacturing & Packaging Technician I Aug1997- Dec 2012
• Completed batch records, cleaning logs, and manufacturing documentation.
• Performed equipment calibration, troubleshooting, and changeovers.
• Conducted cleaning verification and quality inspections.
• Maintained compliance with cGMP, SOP, and FDA standards.
• Assisted with training employees and supervisor coverage. TECHNICAL SKILLS
Production Operations
Manufacturing
Packaging
Inventory Control
Material Handling
Equipment Operation
Quality Control
Documentation
Data Entry
Team Leadership
Customer Service Training &
Support
Pallet Jack Operation
Bilingual (English/Spanish)