Dublin, County Dublin, Ireland
Experienced Technical Consultant specialising in Dynamics CRM with a strong foundation in the Power Platform ecosystem. I have a proven track record of understanding and translating customer requirements into effective business solutions. My project experience from a technical perspective includes custom plugin development with C#, on premise to cloud data migration with KingswaySoft, enhancing UI/UX with JavaScript, implementing & managing a variety of 3rd party integrations with CRM, and automating complex processes with Power Automate. I ensure high quality through effective solution design, development & management practices, with a strong emphasis on reducing complexity while maintaining maximum efficiency. Effectively engaging with stakeholders is at the core of my approach. I enjoy translating technical concepts into clear, actionable insight and have frequently deliver show & tells, workshops, and training. This client-centric approach, combined with four years of project experience has allowed me to gain a well rounded and balanced skillset to ensure I deliver the most effective and high quality solutions.
Lead Dynamics CRM/Power Apps Developer Core Duties Include: - Optimization of existing workflows and processes. - Reduction of system complexity and refining system design. - Documentation and Solution Design - 3rd Party Integration Development & Maintenance - Configuration/Development of Power Automate Flows, Workflows, Plugins - Support to the wider business team & front-end engineering team for CRM integration requirements
Experienced Technical Consultant specialising in Dynamics CRM with a strong foundation in the Power Platform ecosystem. I have a proven track record of understanding and translating customer requirements into effective business solutions. My project experience from a technical perspective includes custom plugin development with C#, on premise to cloud data migration with KingswaySoft, enhancing UI/UX with JavaScript on portals and model driven apps, and automating complex processes with Power Automate. I ensure high quality through effective solution management and deployment practices, with a strong emphasis on thorough testing. Effectively engaging with the client is at the core of my approach. I enjoy translating technical concepts into clear, actionable insight and have frequently delivered show & tells, workshops, and training. This client-centric approach, combined with three years of project experience has allowed me to gain a well rounded and balanced skillset to ensure I deliver the most effective and high quality solutions.
Worked as an Upstream SUBs (Single Use Bioreactors) Production Specialist. This was a diverse start-up project involving all aspects of getting the SUBS process area GMP released, to the production of GMP batches for clinical use. Main job duties included: -Redlining SOP documentation for process area qualification start-up. -Support with studies and engineering batches prior to GMP area release -EMPQ duties – supported and enabled RFT on mapping, flow paths, equipment and furniture fit-out of upstream and downstream SUB suite areas. Also contributed to equipment cleans and dynamic monitoring requirements. -Supporting GMP area release with general process area contributions. -Supported IOQ of small equipment for SUBs. -Compliance on all training requirements. -Daily maintenance tasks on SUBs analytical equipment. -Access to main network platforms for all aspects of job duties - OPM, BMRAM, QUMAS, Historian, NOVA, Steris washers, LIMS. Upstream operator duties - -Media preparations and media sampling -SUB bag preparation and functional testing, -Cell Inoculation, Daily Sampling, NOVA maintenance and testing of samples, -Liaising with QC and QA for manufacturing requirements, -Stringent documentation and adherence to protocols, MRs, SOPs, and batch-sheets, -Online and offline monitoring for cell parameters, and all aspects of Harvest Duties.
QC Micro Analyst with main job duties including: • Bioburden testing of WFI, Potable, Pre-treatment, MilliQ, and Cleaning Validation water samples. • Handling, incubation, and plate reading of all Environmental Monitoring and Bioburden water samples. • Biological indicator testing. • Endotoxin testing of water samples. • Streaking and incubation of all OOS Environmental Monitoring and Bioburden samples. • Responsible for the shipment of all Alert, Action, and OOS samples for Microbial Identification. • Recording all microbial ID results and reporting of Objectionable Organisms. • Strict adherence to GMP, GDP, and GLP. • Ensuring training is complete and up to date.
Chanelle pharmaceuticals headquarters is based in Loughrea, Co.Galway and specializes in the development and production of generic pharmaceutical drugs. Since my induction at Chanelle, I have had a diverse role, with various responsibilities including: • Documentation, upkeep, and organization of raw HPLC data. • Data processing with regular maintenance of stability tables for each product • Drug formulation, manufacture, and associated process validation for each product. • Regular instrument calibrations. • Reporting deviations/OOS data. • Maintenance of HPLC logbooks, column usage logs, formulation logs, and general usage logs. • Retrieval and organization of large amounts of stability products for associated analysis/shipments.