
Proven Quality Assurance Specialist with a track record of enhancing quality standards at Lonza Pharma & Biotech. Leveraged data analysis and meticulous attention to detail to reduce procedural deviations by over 30%. Skilled in materials inspection and fostering a culture of continuous improvement, demonstrating exceptional teamwork and problem-solving abilities.
Stocks cleanroom suites and supports areas with released inventory.
Supports cleanroom environment maintenance at below alerts limits by following established cleaning practice.
Monitors expiry of critical raw materials as needed.
Complies with processes, procedures and instructions for all activities in which the team participates.
Perform procedures according to written guidelines and recognizes deviations from accepted practice.
Responsible for carrying out production processes in a GMP facility, with task including cell culture.
Perform equipment calibrations.
Perform Cell Counts.
IV Certified(Sterile Product and Compounding)
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