Quality Assurance Technician


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https://www.teamhorizon.ie/job-search/991-quality-assurance-technician/quality/sligo/job2023-06-26 14:00:351970-01-01Team Horizon
Job TypeContractor
AreaSligo, IrelandSligoIreland
SectorQuality
Start Date
AdvertiserAshling Guthrie
Job Ref2978
Job Views1592
Description
Team Horizon currently has an exciting opening for a Quality Assurance Technicians to work on our client’s medical device manufacturing facility in Sligo.

 

Why you should apply:



  • Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.


 

What you will bedoing:



  • Work as a member of the Quality Team to ensure that Quality goals and objectives are achieved.


  • Ensure that all actions comply with current good manufacturing practices.


  • Operate within the QC/ IQA and Metrology Areas, as required


  • Complete incoming product testing per the relevant approved specifications and procedures.


  • Complete in-process and final release product testing per the relevant approved specifications and procedures.


  • Ensure Management is kept informed of all Quality Events or potential Quality Events Related to the product or process.


  • Ensure all Quality System documentation is thorough, complete, and compliant.


  • Audit the quality system with other personnel where required.


  • Support Change Management Process including Product and Quality System document review and updates.


  • Generate and Providing metrics for inclusion in the management review, monthly reports and overall Quality Performance


  • Ensure compliance to training requirements is maintained.


  • Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems at the site.


  • Generate batch records for as required in support of manufacturing process orders.


  • Complete disposition decisions for incoming material


 

 

What you need to apply:



  • A third level qualification in a Science/Engineering or other appropriate discipline


  • Minimum of 3 years experience within a regulated GMP environment


  • High level of attention to detail and focus


  • Ability to adapt to new processes on a regular basis.


 
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