Facebook Pixel Code

IT Quality System Analyst - Join a leading Biotech company (Permanent)

LOCATION
Limerick, Limerick, Ireland
APPLY BY
Expired
SALARY
TBC
APPLICATIONS
0 People

IT Quality System Analyst (LMS)

My client offers a unique, world-class opportunity for IT Quality System Analyst (LMS).

The company is one of the top employers in the pharmaceutical and biotechnology companies and is fully committed to bringing their award winning approach to their Irish entity.

In order to reinforce their team, we are looking for a motivated new member.

Tasks:

  • Supporting business user needs of the Learning Management System (LMS) including creating user accounts, answering end user questions and training
  • Administering current LMS environment, developing new business opportunities and improving existing processes
  • Configuration of the Compliance Wire software to meet end-user needs
  • Processes system change control, documents configuration and writing of test plan
  • Providing end-user support for the LMS (Compliance Wire) including troubleshooting problems at the application and server level
  • Identifying and resolving system issues and appropriately communicating items to management, business process owner and users
  • Performing daily business administrative tasks related to functional support and general user account administration
  • Providing SME support and working closely with functional departments on LMS projects to develop, implement and enhance the system
  • Assisting System Administrator with problem solving and implementation of solutions
  • Demonstrating the ability to perform detail-oriented work with a high degree of accuracy
  • Supporting and maintaining system processes, procedures and controls for LMS ensuring compliance with current Good Manufacturing Practices (cGMP)
  • Producing reports/generates data as requested

Requirements:

  • 2 years of relevant experience, Compliance Wire/ Enterprise Learning Management System experience
  • Knowledge of Crystal Reports/Business Objects is a plus
  • Knowledge of 21 CFR Part11, Annex 11 Regulations and Good Manufacturing Practice (GMP)

This is an opportunity to join a team that is already leading the way in the Pharmaceutical/Biotech industry.

Location: Limerick, Ireland

Sorry this application deadline for this job has passed, please look below for related jobs.