Conducted environmental monitoring microbiology activities to maintain clean room standards and ensure GMP compliance. Collaborated with cross-functional teams to implement quality control measures and support investigations. Contributed to process improvement initiatives while adhering to industry and regulatory standards.

Participated in GMP production of viral products through large scale mammalian cell culture and column chromatography with aseptic technique. Drafted and revised manufacturing documents including Batch Records, Specifications, Forms, Change Controls, Deviations, and SOPs. Conducted buffer and component preparation, operated steam autoclave, and supported routine clinical production with manual, semi-automated, and automated equipment. Assisted in fill finish of viral products, cell banking, validation, changeover, data collection, and troubleshooting of process equipment.

I provide validation services across the U.S. for molecular diagnostic PCR panels, including respiratory pathogens, urinary tract infection (UTI), wound, nail, sexually transmitted infection (STI), and antibiotic resistance panels. My expertise helps labs achieve high standards in test accuracy and reliability. Conduct end-to-end validation of RT-PCR kits, ensuring accuracy, sensitivity, and specificity. Perform precision, reproducibility, cross-reactivity, and interference testing to maintain data integrity. Document validation procedures comprehensively for research-use compliance. Train lab personnel on RT-PCR setup, troubleshooting, and result interpretation, emphasizing GLP standards.

Quality Assurance and DocumentationAPI Renewal and Validation Report Binder: Keeping records of API (American Proficiency Institute) renewals and validation reports.IQCP Document: Individualized Quality Control Plan, ensuring quality control and quality assurance with a laboratory director's signature.Risk Acceptability: Assessing risk factors related to specimens, testing personnel, reagents, environment, test systems, and test results.SOP Binder: Standard Operating Procedures documentation.Proficiency Testing Binder: Records of proficiency testing to ensure laboratory accuracy.Equipment Maintenance Binder: Documentation of maintenance activities on laboratory equipment.Calibration and MaintenanceQuant Studio Machines: Ensuring these real-time PCR machines are properly calibrated and updated for accurate results.

NGS, Gentech toxicology. High-Performance Liquid Chromatography (HPLC), Agilent 1260 Infinity Series: Proficient in operating and maintaining this robust HPLC system for high-throughput and high-resolution analysis. Experienced in method development and optimization for complex sample analyses in a regulatory compliance environment. Mass Spectrometry, Agilent 6460 Triple Quadrupole LC/MS: Skilled in utilizing this advanced mass spectrometry system for quantifying low-level compounds in diverse matrices. Expert in conducting sensitive and specific quantitative analyses critical for clinical research, environmental testing, and forensic studies.

Responsible for overseeing lifeguard team and ensuring safety protocols were followed.Conducted regular safety drills and maintained pool cleanliness.Provided first aid and emergency response as needed.

Assisted Project Manager in planning and executing construction projects.Coordinated with subcontractors and suppliers to ensure timely project completion.Managed project documentation and ensured compliance with safety regulations.

Managed client accounts and provided exceptional customer service.Developed sales strategies to achieve company targets.Prepared reports on account status and communicated regularly with clients.

Led the sales team and developed sales strategies to increase revenue.Conducted market research to identify new sales opportunities.Trained and mentored sales staff to improve performance.Booking.com, Expedia, Hotels.com etc.