I have 17+ years of experience in the Medical Sciences, focusing on precision, problem-solving, and producing quality results. I thrive in fast-paced environments and building collaborative relationships with diverse teams. My track record reflects my dependability, passion, attention to detail, and excellent organizational skills. With a proven ability to address complex medical device and instrument issues, I firmly believe that my professional skills and experience make me an outstanding candidate for any organization.
· Provide remote software and connectivity support for the following medical laboratory instruments:
Vitek 2, Vitek 2 compact, Vitek Reveal, BacT, MYLA, Corepoint, BACT/Alert, Virtuo and Previ isola.
· Meet monthly and annual performance and quality metrics set forth by department leadership.
· Collaborate and produce innovative solutions to enhance the customer’s experience when contacting the Software support line for troubleshooting or questions.
· High-performance remarks and customer feedback for providing prompt and accurate assistance and fixing the issue within the time limits set forth by the department.
● Conduct air and surface sampling in isolation 5 and 7 clean rooms while facilitating personnel and product sampling for sterility and purity
● Upheld company's quality standards in revitalizing SOPs to remain current with cGMP policies and FDA regulations
● Maintain FDA performance standards in isolating and testing microbes from clean room samples and personnel
● Prioritize supervisory tasks in coordinating with a 15-member team to achieve short and long-term goals
● Boost productivity by executing time-sensitive laboratory activities to deliver high-quality pharmaceutical products
● Headed new instrumentation implementation for the Bruker Maldi-TOF. This included technical writing of the IOQ-PV and new instrument protocols, along with writing the corresponding SOP and training documentation.
● Exercised keen attention to detail by processing and preparing specimens for microbiology and molecular testing in a timely manner
● Managed competing tasks by initiating routine bench plate reading and identification and susceptibility testing of pathogenic bacteria
● Achieved organizational objectives by running PCR testing for COVID-19, C-diff, and MRSA while following all hospital, FDA, CDC, and CAP protocols for reporting and testing of biological substances
● Performed routine bench workup of pathogenic bacteria, including identification and susceptibility testing of pathogens using the VitekII system and biochemical reagents
● Supported project deliverables by processing and plating specimens and conducting molecular and serological tests to analyze and report patient results accurately
● Ensured quality control by performing routine maintenance on automated systems, biochemicals, and media while efficiently analyzing Panther resulting work lists for errors
● Streamlined antimicrobial testing and identification using Vitek II, Microscan Analog, Bactec Alert, and Biomerieux mass spectrometry machines
● Maintained quality assurance and control standards by aligning with proper protocols set by CAP, FDA, CDC, JHCO, and CLIA
● Assured data integrity by accurately tracking and reporting findings to detect and decrease errors by 85%
● Coordinated the identification and workup of aerobic, anaerobic bacteria, and mycobacteria pathogens while performing antimicrobial susceptibility testing
● Delivered quality results by discriminating between relevant normal flora and pathogenic bacteria, reading gram stains, and conducting quality control on reagents, media, and other miscellaneous items
● Supported various research projects by instituting cost-effective solutions for media and reagent use
● Enhanced efficiencies by collaborating with a 28-member team to decrease turnaround times for culture workup and gram stains by 70%
● Executed diverse tasks by ordering culture tests, reviewing gram stains, initiating antimicrobial sensitivity testing, and identifying infectious bacteria, mycobacterium, and fungal elements
● Produced accurate results by differentiating between pathogens and normal flora within immunodeficient and healthy patient populations
● Optimized workflow by improving the documentation of problems and errors to eliminate future mistakes