This Job Vacancy has Expired!

Senior Manufacturing Quality Engineer

Posted on May 15, 2020 by Real Staffing Group

Clare, Ireland
Engineering
Immediate Start
Annual Salary
Full-Time




Title: Senior Manufacturing Quality Engineer



Location: Clare



Benefits: Opportunity for career progression, salary, pension, healthcare and yearly bonus.



Company:



My client are a Medical Device multinational who manufactures and markets products that simplify, automate and innovate complex biomedical tests.



Responsibilities:





  • Co-ordinate the Manufacturing Non-conformance process (NC) for all Production areas ensuring compliance to Quality and Regulatory Standards.


  • Lead cross functional teams providing Quality guidance and support.


  • Responsible for the Rework process, ensuring relevant documentation is prepared.


  • Execute the Stop Ship process for finished product released to the market


  • Responsible for ensuring the Manufacturing Quality Procedures are current and in line with global procedures


  • Initiate/review/approve document Change Controls (CCFs) and Equipment Change Controls (ECCs)


  • Ensure quality issues are communicated to the management team such that they are aware of any potential problems or opportunities


  • Review/approve Validation documentation (eg protocols, reports) ensuring compliance to applicable procedures.


  • Generate, update, implement and complete associated training for relevant departmental procedures, as required.


  • Assist in the Supplier Quality process acting as a Supplier Quality representative, if applicable


  • Assist with the QA review & disposition of Batch History Records (BHRs) for all product lines and complete the associated ERP activities ensuring relevant logs and BHRs are maintained.


  • Perform CAPA (corrective and preventive action) activities and document in the Global CAPA system if required.




Experience required:





  • Bachelor' s degree in chemistry, biochemistry, engineering or other relevant technical field with a minimum of 3 years' experience in a highly regulated industry.


  • Desirable to have previous experience in IVDDs and Manufacturing Quality.


  • Good knowledge of ISO9001/ISO13485, FDA and GMP requirements.


  • Excellent time management, planning and organisation skills.


  • Must have a working visa for Ireland




If you are interested in applying or hearing more about this opportunity and others like it, forward a copy of your update CV.



Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales







Reference: 888195701

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