Emir P.
Cclas Consultant @Datamine
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WORK HISTORY
Cclas Consultant @Datamine
GB
As a Consultant at Datamine, I lead the implementation of projects and designs in accordance with industry best practices, managing scope, tasks, risks, and ensuring client satisfaction. I provide consultancy services, SQL Server/Visual BasicScripting, prototype presentations, and demonstrate CCLAS applications, and deliver post-sale support for Labratory Information Management Systems. Additionally, I engage in marketing efforts to grow Datamine’s presence in Europe and the Middle East, delivering presentations and demonstrations of CCLAS capabilities. I also contribute to product development through client feedback, customise training programs. I actively contribute to industry knowledge by reviewing peer-reviewed articles, presenting for clients, and continously improving implementation methodologies.
EDUCATION
Rutgers University - Camden
Associate of Science - AS, Biomedical/Medical Engineering
University of South Wales
Bachelor of Science - BS, Biology (Honours)
University of Essex
Master of Science - MS, Infection Control
ABOUT EMIR P.
Dedicated Microbiologist with a discipline in microbiology, infectious diseases, pharmaceutical manufacturing, medical devices, and research and development.Demonstrated history within the pharmaceutical and medical device sector, specifically microbiology, thereby possessing an extensive skillset including cGMP, GLP, and GDP. Experienced in pharmaceutical manufacturing, R&D, and the medical device industry.Also experienced with environmental monitoring, bioburden, endotoxin, fertility, and sterility testing for bulk intermediates to finished products and coordinating the microbiology lab accordingly. Proficient within LIMS, dedicated to professional development plans, quality improvement projects, and analytically identifying, trending, and projecting statistical change of microbes within the pharmaceutical site.Moreover, fully capable of assessing new medical devices, and formulating protocols for testing, mainly to assess/test bioburden, biological indicators, direct inoculation, bacteriostasis and fungistasis, endotoxin, inter alia. Furthermore, proficient in leading VDMax studies thereby calculating verification doses for irradiation (gamma, X-ray, ethylene oxide, vaporized hydrogen peroxide, and electron beam), thus ensuring sterilization and decontamination of healthcare products in line with ISO and 11737, and R&D projects adhering to ISO 13485.Additionally, possess exemplary experience conducting root-cause-analysis investigations for out-of-specification results and leading deviations. Experienced with continuous quality improvements and committed to professional development plans.Notwithstanding, I am clinically qualified for an Infection Control Practitioner role, equipped with a particular interest in microbiology, communicable diseases, disease control, epidemiology, outbreak management, and advanced practice in healthcare; all whilst adhering to clinical governance frameworks and best practices; however, I am not currently practising as a practitioner.
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