QA Specialist


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https://www.teamhorizon.ie/job-search/850-qa-specialist/quality/cork/job2023-02-14 16:01:021970-01-01Team Horizon
Job TypePermanent
AreaCork, IrelandCorkIreland
SectorQuality
Start Date
AdvertiserAshling Guthrie
Job Ref#2823
Job Views1505
Description
Do you want to be part of a Great Place to Work? Team Horizon is seeking a QA Specialist on behalf of a global, research-based biopharmaceutical company that combines leading-edge biotech with the expertise and capability of an established pharmaceutical leader.

 

 

Why you should apply:



  • There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.


  • Jpin a company whose goal is to help patients live healthier lives and are proud to be a Great Place to Work.


 

What you will be doing:



  • Reviewing all documentation associated with batch release to ensure GMP compliance.


  • Reviewing and investigating of complaints


  • Ensuring the follow-up of the necessary corrective actions & preventative actions implemented in consequence of a quality failure


  • By performing investigations, and ensuring a follow-up, following discrepancy, failures and external complaints.


  • Participate in KPI meetings to assist the batch release process.


  • Reviewing the GMP documentation eg, SOPs, reports, methods, specifications, validation protocols, quality contracts etc.


  • By carrying the inspection, investigation, and taking of samples where appropriate, in order to monitor factors which may affect product quality.


  • Any other duties as assigned 


 

What you need to apply:



  • Bachelor’s Degree preferably in technical or scientific area (Chemistry, Pharmacy, Biology, Microbiology, or Engineering) or equivalent industry experience (at least 3 years) with sufficient exposure to pharmaceutical, medical device, or combination product related industries a significant advantage.


  • Ideally, you would have a technical background and understanding of the audit process and knowledge of worldwide requirements related to GMP regulations for quality systems and compliance.


  • Proficient in Microsoft Word & Microsoft Excel


  • Excellent written and oral English communication skills.


 

 

 
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