QC Analyst at Werfen (2025-08 – Present)
Performs analyses of Clinical Chemistry, Critical Care, coagulation and microbiology controls and reagents using various automated techniques in accordance with established quality standards and GMP requirements.
- Performs analyses of Clinical Chemistry, Critical Care, coagulation and microbiology controls and reagents using various automated techniques in accordance with established quality standards and GMP requirements
- Perform automated and manual assays as detailed in departmental/plant SOPs and QC Monographs including raw material, in-process and finished products
- Interprets test results against specifications and decides if assays pass or fail
- Maintains documentation of all work performed in accordance with GMP requirements
- Performs product stability, proficiency, environmental testing and water system testing
- Used In Vitro instrument to determine accurate concentration of relevant blood gases and electrolytes in the sample
QA Lab Tech at Star Kay White (2024-02 – 2025-07)
Full-time position focused on quality assurance testing and inspection of candy production.
- Inspected Labels, Metal Detectors, and thermometers, preventing allergens and foreign material, resulting in enhanced product quality and adherence to regulatory standards
- Executed comprehensive inspections of 5 rooms in the Candy production area, detecting and addressing allergens and signs of uncleanness, ensuring the company's high standards
- Contributed to cost savings by optimizing the viscosity testing process with Bostwick and Brookfield instruments, resulting in 20% reduction in testing time
- Utilized water activity meter to verify proper water content in products, contributing to a 10% reduction in product defects and ensuring compliance with industry standards
- Improved accuracy of sugar measurement by implementing Brix/Refractive Index method, resulting in a 15% reduction in measurement errors and ensuring product quality
- Consistently ensured pH levels within spec without sample prep, contributing to 5% reduction in product rework
- Consistently provided accurate moisture and fat content data for X product samples, enabling informed customer purchasing decisions and satisfaction
- Conducted daily review of product retains, upholding product uniformity and identifying any anomalies, ensuring high product quality
Analytical Chemist at PDI (2020-06 – 2023-04)
Managed and executed all chemical testing procedures with focus on productivity and quality improvements.
- Managed and executed all chemical testing procedures, resulting in a 20% increase in productivity and a 10% decrease in testing errors. The company was able to meet customer demand and maintain a competitive edge
- Utilized wet chemical titrations to accurately measure and record the purity of raw materials, resulting in 100% batch consistency
- Improved testing efficiency by analyzing active percentage using IR, UV, Auto-titrator. Reduced turnaround time by 20%
- Developed and validated analytical methods that enabled the company to meet quality standards, leading to a 100% compliance rate
- Enhanced quality assurance by certifying chemical and component accuracy through meticulous testing. 100% timely release
- Maintained the production schedule through efficient sampling, testing, and release of raw materials, ensuring timely delivery of products
- Improved vendor relations by negotiating lower prices for lab supplies, saving company $50,000 annually
- Conducted thorough analysis of finished goods, collaborating with manufacturing floor to optimize production processes. Reduced manufacturing time by 20%, saving $50,000 annually
- Improved data accuracy by 15% through meticulous use of LIMS software, leading to more reliable experimental results and increased client satisfaction
- Optimized production schedules and improved product quality by 12% through diligent team collaboration and efficient laboratory support
- Possess a proven track record in Out-of-Specification (OOS) investigations. Successfully deconstructed issues in 100% of OOS investigations, resulting in a 50% decrease in overall OOS occurrences
- Reduced testing errors by 10% within 3 years through the implementation of rigorous quality control measures, enhancing overall data reliability
- Executed various wet chemistry techniques, including titrations and TLC, ensuring 100% accuracy in test results and enhancing overall lab efficiency within 6 months
