PharmEng Technology
Elizabeth Caramaroudis has a diverse work experience in the pharmaceutical industry. Elizabeth started their career at Apotex Inc. in 2008 as a Microbiologist, where they were responsible for sterility testing of raw materials, in-process, final product, and environmental testing. Elizabeth ensured compliance with operational standards and executed accurate testing to ensure sterility throughout the process.
In 2010, they joined Novartis as a Sterile Team Leader. In this role, they monitored aseptic operations and operator techniques to ensure the production of high-quality ophthalmic products in controlled clean rooms. Elizabeth investigated deviations, determined root causes, and implemented corrective actions to maintain a robust quality control system. Elizabeth also ensured the required production environmental conditions through the EMS system.
Since 2015, Elizabeth has been working at PharmEng Technology. Initially, they served as a Senior Validation Consultant, and later became a Project Manager Thermal Validation. Further details about their roles and responsibilities at PharmEng Technology were not provided.
Elizabeth Caramaroudis has studied Industrial Microbiology with a focus on Biotechnology at Centennial College. Additionally, they have pursued studies in Life Sciences at the University of Toronto Scarborough. Unfortunately, the specific start and end years for both educational experiences are not provided.
PharmEng Technology
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PharmEng Technology is a leading global provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes. Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique needs and challenges. At PharmEng Technology, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives and develop customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs. As a trusted partner to some of the world's largest pharmaceutical companies, we have a proven track record of success in delivering high-quality technical services and solutions that drive operational efficiency, reduce costs, and enhance overall performance. We are dedicated to helping our clients succeed in an ever-evolving and highly competitive industry. At PharmEng Technology, we are passionate about what we do, and we are committed to delivering excellence in everything we do. Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).