My main responsibilities include analysing and developing analytical pipelines for internal and external customer data for ChemStress®.Managing and operating a Data Warehouse for CellAI® data management.

Age groups 4-6; I coached and helped develop juvenile GAA in Nursery groups that involved introductory skills and games. Age groups 14-18; I contributed to the development and coaching of young men in this age bracket by attending training sessions, helping in coaching the skills of the game and provided strength and conditioning programmes.I enrolled in safeguarding courses level 1 – 3, child welfare and protection in sport, club children’s officer and designated liaison person… Show more Age groups 4-6; I coached and helped develop juvenile GAA in Nursery groups that involved introductory skills and games. Age groups 14-18; I contributed to the development and coaching of young men in this age bracket by attending training sessions, helping in coaching the skills of the game and provided strength and conditioning programmes.I enrolled in safeguarding courses level 1 – 3, child welfare and protection in sport, club children’s officer and designated liaison person training.d Show less

I supported vaccine commercial and clinical manufacturing, vaccine stability studies and orphan-disease product release as part of the Quality Control Vaccine Finished Product Testing team. My responsibilities for Prevnar 13 (13vPnC) vaccine included:Determining the immunological serotype specificity of total and adjuvant-bound antigenicity and the conjugated antigenicity of the 13 purified bacterial pneumococcal strains present in the 13vPnC finished product by rate… Show more I supported vaccine commercial and clinical manufacturing, vaccine stability studies and orphan-disease product release as part of the Quality Control Vaccine Finished Product Testing team. My responsibilities for Prevnar 13 (13vPnC) vaccine included:Determining the immunological serotype specificity of total and adjuvant-bound antigenicity and the conjugated antigenicity of the 13 purified bacterial pneumococcal strains present in the 13vPnC finished product by rate Nephelometry. Determining the total and adjuvant-bound protein concentration by Modified Lowry assay. Determining excipient concentration that include Succinate, 2-Phenoxyethanol and Polysorbate 80 concentration by HPLC.Compendial analysis that include pH, volume of injection and appearance analysis. My responsibilities for Elelyso (Taliglucerase Alfa) commercial release and stability study support included:Purity determination by size exclusion HPLC and reverse phase HPLC.Other responsibilities included: Responsibility for investigating analytical instrumentation calibration events and determining whether the instrument is to be deemed fit for purpose after such incidences. Responsibility for reviewing Regulatory Pharmacopeia compendial notifications to determine if an amendment or update will affect the current testing of Prevnar, Trumemba and Elelyso. Responsibility for organising incoming and outgoing product and materials to support reference standard and reference materials stock levels as well liaison with onsite regulatory team to ensure effective supply of such materials to new emerging markets and site to site technical transfer. Show less

Actively supported commercial and clinical manufacturing as part of the Biochemistry/Microbiology/Chemistry In-Process Quality Control Janssen Supply Chain team.Member of the QC EHS cross functional team.Member of the QC 5S implementation team.Member of the QC Laboratory Execution System (LES) and Smartlab transfer team. Main responsibilities included:Determination of protein concentration by Ultra-Violet Analysis and Nephlometric Assay… Show more Actively supported commercial and clinical manufacturing as part of the Biochemistry/Microbiology/Chemistry In-Process Quality Control Janssen Supply Chain team.Member of the QC EHS cross functional team.Member of the QC 5S implementation team.Member of the QC Laboratory Execution System (LES) and Smartlab transfer team. Main responsibilities included:Determination of protein concentration by Ultra-Violet Analysis and Nephlometric Assay (IgG).Quantitative determination of Monoclonal Antibody by Protein A and Protein G HPLC. Determination of endotoxin concentration by Kinetic Quantitative Chromagenic Lysate Assay and by the Endosafe PTS reader assay.Characterization of protein by Double Radial Immuno Diffusion Assay [(DRID) Ouchterlony].Colour of solution testing (ESP/USP).Routine operation, calibration, maintenance and troubleshooting of equipment and its associated software.Routine upstream and downstream sample management as part of the In-Process and Drug Product Release cross functional team.Determination of residual protein by Dot Blot analysis and Colloidal Gold staining assay.Support cell culture new product introduction through analytical process development for Protein A/Protein G HPLC. Support direct product capture for downstream purification through colloidal gold buffer and residual mock elution cleaning verification studies. Show less

Main responsibilities which included:Serving CustomersWaiterStock ControlCleaning and Maintainence

Five main responsibilites which included:Bioburden TestingEndotoxin TestingEnvironmental MonitoringSterility Testing/AssuranceChemistry Testing that includes Salt Assay, TOC, Metal Assays, Water Analysis, Ultra-Violet and Sub-Visible Analysis

Responsible for filing gynecology and obstetrics records by updating historic files in accordance with ACOG to Microsoft Excel.