Sylvia Rytel

Currently, I am a Technical Specialist/QAU at LifeSign, where I review, comply, update, and prepare SOPs. I also maintain and monitor quality assurance and QC practices and procedures, and handle product complaints and reporting.

During my seasonal employment for the FluMist vaccine, I provided QA oversight of aseptic processing, including executing personnel monitoring using the MODA system. I also conducted real-time review of batch records, logbooks, and other GMP documents.

I was responsible for interacting and coordinating closing dates and locations with lenders, realtors, buyers, and sellers. I prepared all documents required for closing, ensuring proper execution and notarization, and obtained funding approval.

I reviewed batch records, laboratory notebooks, and instrumentation logbooks for accuracy and completeness. I also performed quality reviews and approvals of validation documents, including protocols, reports, and analytical test methods.

I worked under ISO 6 cleanroom conditions, performing plate incubation, rotation, reading, and reporting results. I also maintained a monthly employee gowning test and conducted air particle measurements.

As a Quality Assurance Coordinator, I efficiently coordinated and executed workflow throughout packaging operations, ensuring safety, sanitation, productivity, and customer satisfaction. I collaborated with the Director of Quality on procedures, training, customer complaints, and record-keeping.

As a Quality Assurance Specialist, I contributed to maintaining quality standards. My responsibilities included ensuring compliance with regulatory guidelines and supporting quality control processes.

Studied Pharmaceutical Science, gaining a strong foundation in the field. Developed skills relevant to the pharmaceutical industry.