Skip to main content

Senior QC Compliance Specialist

  1. NI & Ireland
  1. Contract
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.

Please note, Quanta Consultancy Services does not sponsor Visa applications.

To view Quanta's privacy policy, please visit our website

Send us your CV

Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.