Emmanuella Adjei Poliah

Assistant Project Manager at Guy's and St Thomas'​ NHS Foundation Trust
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Contact Information
us****@****om
(386) 825-5501
Location
London, England, United Kingdom, UK
Languages
  • Akan -

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Experience

    • United Kingdom
    • Hospitals and Health Care
    • 700 & Above Employee
    • Assistant Project Manager
      • Aug 2019 - Present

    • Project Coordinator
      • Oct 2017 - Aug 2019

      Provided administrative support to the Programme Manager and Programme Diretor to deliver multimillion pound projects.

    • United Kingdom
    • Museums, Historical Sites, and Zoos
    • 700 & Above Employee
    • Exhibition Volunteer
      • Feb 2017 - 2018

      My duties include: - Interact with visitors and talk to them about the displays in the museum - Object handling My duties include: - Interact with visitors and talk to them about the displays in the museum - Object handling

    • United Kingdom
    • Government Administration
    • 700 & Above Employee
    • Scientist
      • Jul 2015 - Sep 2017

      Undertake testing of Plasma Pools for evidence of viral contamination thus ensuring the safety of medicinal products derived from human blood. My main duties include: • Developing International Standards and Reference Panels used in a range of establishments such as hospitals and manufacturing. • Proofreading complicated scientific documents for bodies such as the Standards Programme Board. • Developing and maintaining SOPs (Standard Operating Procedure) and risk assessments, ensuing they are document controlled, reviewed and reissued in a timely manner. • Liaise and collaborate with internal and external stakeholders regarding a variety of matters for example ensuring clients send correct samples along with relevant documents. • Validating new equipment ensuring appropriate quality standards are applied in accordance to regulatory requirements. • Use of various data management systems such as LIMS (Laboratory Information Management System) to document, store, organise and analyse data to be used in presentations and conferences. • Managing sample lifecycle in my laboratory thus ensuring that all relevant tests were complete and compliant. • Maintaining stock levels in multiple laboratories and ensuring the use of equipment and consumables in a cost effective manner. Show less

    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Quality Control Product Analyst
      • May 2013 - Jul 2015

      Performance of qualitative and quantitative analytical test methods on new and existing products in order to maintain good quality control and good environmental standards. My duties include: • Investigating root causes of failures in test methods; carrying out experiments, collating data and looking at trends to decipher possible root causes thus leading up to appropriate CAPAs. • Checking and amending documentation and processes to ensure they comply with GMP (Good Manufacturing Practice) and national and international regulatory bodies such as the MHRA. • Performing analytical tests in accordance to relevant policies and regulations and ensuring the delivery of results to different departments in a timely manner. • Regular use of data management systems. • Providing specialist training, advice and support in laboratories, ensuring staff are competent enough to perform activities without supervision. • Regular interaction with stakeholders to share project updates and documentation through appropriate communication channels. • Daily use of Microsoft programmes. Show less

    • Switzerland
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Quality Control Microbiologist
      • Sep 2011 - May 2013

      Performance of microbiological analysis on intermediate and final product samples, raw materials, water systems and environmental samples. My duties included: • Raised and documented deviations with supporting evidence in accordance with defined procedures and investigating and identifying root causes thus leading to CAPAs. • Involved with laboratory audits, ensuring that the working area and documentation was audit ready in an event of a regulatory inspection by the MHRA and other regulatory bodies. • Creating monthly environmental monitoring reports by extracting information and trended data from various programmes such as Microsoft Excel then putting it into clear, translatable formats such as pivot tables and graphs or PowerPoint presentations. • Regular use of data management software e.g. LIMS (Laboratory Information Management System) to record, store and retrieve results. • Project managed an investigation into using different types of equipment in environmental monitoring. • Reviewed, amended, approved and signed-off documentation, ensuring completed documents were compliant with the regulatory governing bodies and GMP. • Involved in departmental improvement projects such as finding ways to improve the working environment and enhancing the work-flow process, from testing to the completion of documentation. • Trained new and existing members of staff on performing various test methods which contributed to the smooth running of the annual manufacturing shutdown. Show less

Education

  • Brunel University
    Bachelor of Science (BSc), Biomedical Sciences, General
    2007 - 2010
  • King Edward's Witley
    GCSEs
  • Lansdowne College
    A-Levels

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