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Senior QC Compliance Specialist

  1. NI & Ireland
  1. Contract
Competitive
24811 JL
  1. Compliance / Quality Assurance
Date Posted17 Jul 2020
 Senior QC (Quality Control) Compliance Specialist - Republic of Ireland


A Leading midlands-based biotechnology organization requires a Senior QC (Quality Control)Compliance Specialist to support their growing GMP laboratory at its state-of-the-art manufacturing facility in Ireland. This role will identify and implement process and compliance improvement opportunities.

We are looking for someone from a Microbiology background for this position with experience in Continuous Improvements - ideally holds a yellow or green belt. 



Key responsibilities
  • 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 targets
  • Develop simplified and effective scheduling for routine/non routine activities to maximize available resources
  • 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.
 

Experience Required
  • Extensive experience working in a GMP Quality Control Laboratory
  • MSc. Degree in science/pharmaceutical related subject
  • Knowledge and understanding of GMP/GDP standards
  • 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 others
  • Good working knowledge of QC Microbiology and Chemistry instrumentation and methods
  • An ability to work independently, as well as a member of a team in a dynamic, fast-paced environment.
  • Excellent communication & presentation skills are essential.
  • Excellent time management organizational skills along with a proven ability to multi-task.
     
Please apply with your CV now for this contract opportunity for a chance to work with a growing global organization within their expanding laboratory operations.

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

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