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QC Technical Support Specialist

  1. East
Carlow
  1. Contract
Competitive
  1. CAPEX Projects
35148
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QC Technical Support Specialist– Ireland – Contract

Do you want to be involved with exciting pharmaceutical projects?

When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a QC Technical Support Specialist.

This a fantastic opportunity to be involved with the critical investment projects both on-site and remotely.

Essential Duties and Responsibilities for this role include, but are not limited to, the following:
  • Support Quality Control activities in the QO laboratory through documentation generation and investigations associated with GMP activities. 
  • Author/ Provide technical expertise and technical oversight of Investigations, Quality Notification, Out of Process Control Limit OOPCL completion, Be a document system expert; this will include document review, approval and document system workflow expedition.
  • Format, write, deliver, and review necessary documentation in line with the standard approval process, and facilitate others to do so. 
  • Documents will include SOP’s, SWI’s, training documents, and change controls.
  • Support Laboratory activities through documentation generation, filing, tracking, auditing, and efficient maintenance of all associated databases including the maintenance, auditing and archiving of the process documentation system.
  • Support Batch release through timely Investigations, Quality Notification, Out of Process Control Limit OOPCL completion,
  • Interim/summary report generation; meeting batch release requirements.
  • Perform Compendial Assessments. 
  • Author Annual Product Review, Trend Reports. 
  • Raise CAPA's and conduct investigations.
Desirable Experience:
  • Proficiency in Microsoft Office and job-related computer applications required with proven analytical and systematic problem-solving skills
  • Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices
  • Bachelor’s Degree or higher preferred; ideally in a Science, or other Technical discipline
  • Relevant experience in QC Laboratory within GMP setting 
If this role is of interest to you, please apply now!
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