Experience

GSK

• United Kingdom
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Quality Executive and Deputy Responsible Person

  • Dec 2018 - Present

  Providing effective and efficient quality assurance support to QMS. Responsibilities included looking after several procedures such us:- Change controls- Risk Managment- Deviations- CAPAs- Auditing- Product complaints- Annual product quality reviews- Repacking- Incident managmentThe responibilities also included ensuring the quality of product supply. This included activities such as review of Quality Agreements and Technical Terms of Suply, liaising with third parties, submition of documents to regulatory agencies and supporiting supply chain.

• Archiving Administrator

  • Oct 2018 - Dec 2018



Cpl

• Ireland
• Staffing and Recruiting
• 700 & Above Employee

• Pharmacy Intern instructed by GSK

  • Mar 2018 - Sep 2018

  KEY ACCOUNTABILITIES / RESPONSIBILITIES : o Support the LOC Quality Manager to ensure that all internal procedures and systems in use in the LOC are compliant to GSK QMS, Guide for Commercial Companies and local regulatory requirements, including (but not limited to)o Annual Product Quality Reviews– perform annual product quality reviews for GSK pharma products and summarise these reviews in approved report format.o Change Control - perform day to day work to support the local change control process with the aim of ensuring all planned major changes (including as appropriate new pack introduction, product discontinuation, major pack changes, re-packing activities) are effectively and compliantly managed. o Corrective and Preventative Actions (CAPA) – Conduct Root Cause Analysis and develop appropriate CAPA based upon investigations and implement CAPAs to correct and prevent recurrence of issues.o Product Technical Complaints - perform day to day work to support an effective complaints management process ensuring:- complaints are managed using the CERPS CC Notification tool, including:- escalation of potential issues to the LOC Quality Manager and Named Safety Contact for Ireland- reporting and following up on product technical complaints with manufacturing sites, customers and commercial teams.o Incident management – Assist the LOC Quality Manager in any investigations triggered by local incidents and in conducting LOC Incident Committees. o Product supply - performs day to day work to support systems that have an impact on the quality of imported, products in line with the QMS and local Regulatory requirementso Responsible for the review and at the direction of the LOC Quality Manager the approval of TTS (Technical Terms of Supply) and liaison with manufacturing sites to ensure compliance to local registered technical details.



LloydsPharmacy

• United Kingdom
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Pharmacy Intern

  • Sep 2017 - Mar 2018

  I worked as pharmacy intern in Lloyds pharmacy



Trinity College Dublin

• Ireland
• Higher Education
• 700 & Above Employee

• Research Assistant

  • Jun 2017 - Jul 2017

  Working under Dr Sheila Ryder programming a 'Pharmacy 3D Simulator'. I was developing the simulator in Unity Game Engine using C# programming language.



Trinity College Dublin

• Ireland
• Higher Education
• 700 & Above Employee

• Student Intern

  • Jun 2016 - Aug 2016

  During the internship I was creating exercises for the second year of the new pharmacy course in PebblePad E Learning Space. Additionally I was creating tutorials for Pharmacy Students on Community Drug Schemes using Articulate.



University of Vienna

• Austria
• Research Services
• 700 & Above Employee

• Erasmus Traineeship Student

  • Jun 2015 - Sep 2015

  During this Traineeship I was working on Using Lithium Compounds to make Carbon of imine group more susceptible to nucleophilic attack. This research was later used as a fourth year dissertation.