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QC Compliance Specialist

  1. Midlands (Ireland)
  1. Contract
  1. Compliance / Quality Assurance
Date Posted06 Apr 2021
QC Compliance Optimisation Specialist opportunity to work with a Global Bio-Pharmaceutical Organisation at their Manufacturing facility in County Westmeath, Ireland. 

Working hours: 40 hours per week
Working from home: Mixture of remote/ on site. You will need to come to site to get familiar with the lab and facility but then there would be flexibility to work from home on an ongoing basis. 

Ireland is a hive of activity for the Life Sciences Sector at present, with Global Players investing heavily in manufacturing facilities here. 

An excellent opportunity has arisen for an experienced QC Compliance Specialist to join a Global Bio-Pharma facility in County Westmeath. In the role you will be responsible for actively identifying opportunities for process and compliance improvement and translating these into practice.

Principal Responsibilities to include: 

  • Support implementation of effective shift handover/QC internal communication
  • Identify and implement improvements to Lab Processes, Layout/flow and 6S type activities
  • Training: design of induction training to lab, up to area SME level; define the training requirements and implement simplified training program
  • Planning, scheduling and facilitating continuous improvement workshops and translation of the output to procedural/process updates.
  • Documentation flow and paperwork practices: Improving Right First Time and reducing GDP errors within QC and implementing processes to track and trend performance against target
  • Develop simplified and effective scheduling for routine/non routine activities to maximise available resource
  • Implementation of real time review and real time trending of all QC data
  • Support Implementation of in-house microbial identification using the Vitek including the design of process, documentation and training program
  • Maintain regular and proactive communication with all stakeholders.

Desired Experience: 

  • Strong experience working in a GMP Quality Control Laboratory
  • Knowledge and understanding of GMP/GDP standard
  • Strong problem solving and leadership experience
  • Experience in workshop facilitation
  • Experienced in leading and executing continuous improvement initiatives
  • Experience of SOP authoring and document management processes
  • Experience of provision training to other
  • Good working knowledge of QC Microbiology and Chemistry instrumentation and methods

Interested in hearing more? Apply today to be considered for this position!

The candidate must have the rights to work in the location stated in the job advert.

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