Overview

QC Analytical Expert

Location : Waterford
Duration : 6+months

Main Responsibilities:

  • Providing his/her analytical experts for any project, troubleshooting, investigation on analytical methods and lab technologies.
  • Coordinate analytical testing on projects (validation/transfer), ensuring adherence to the committed scheduled plans
  • Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records related to these tasks
  • Recording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and Data integrity requirements
  • Writing/reviewing protocols and reports related to analytical validation/transfers and qualification activities
  • Writing/reviewing and maintaining accurate analytical methods procedures
  • Informing his/her manager of any quality or HSE event (deviations or OOx) in a timely manner to ensure investigation and impact assessment are performed appropriately
  • Participating actively to any investigation, where he/she is involved, to ensure investigations and impact assessment are performed appropriately
  • Performing periodically trend analysis on method performance in order to determine the need to revalidate, optimize or replace the method
  • Ensuring that his/her lab/facilities, lab instruments, are kept in a quality and safety status to ensure that they can be used appropriately
  • Supporting QC teams during internal, external audits and inspections

 Skills and Experience

  • Experience in quality control within the pharmaceutical industry, including knowledge of Good Manufacturing Practices (GMP) and regulatory requirements.
  • Ability to analyse complex data and laboratory results to make informed decisions and identify areas for improvement.
  • Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements.
  • Proficiency in identifying issues and implementing effective solutions to resolve quality control problems.

 Qualifications

  • Higher Level degree in science or equivalent technical discipline
  • 3years + experience within Pharmaceutical Development, Analytical and/or Manufacturing department

 
Candidates should hold appropriate RTWs for Ireland i.e. Stamp1G, Stamp 4, Irish/British/EU passport.  

For more information please apply here or contact Agnes Reena/agnes.reena@eirevo.ie  Contact: 0858564199  

  
Candidates must be eligible to work full time and long term in the location specified or currently hold a valid appropriate long term work Visa to apply.
  
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