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CCP Recruitment
Unit 13A Northpoint, Tuam Road, Galway
Phone: +353 91 730022

Web: www.ccprecruit.ie E-mail: info@ccprecruit.ie

Quality Engineer


MK/33780/IJP

Engineer Quality Engineer Quality

Cork Cork city Munster

Negotiable

2 - 3 Years

Permanent Full-time

Third Level Degree

Michelle Kilcar

michelle@ccprecruit.ie


Quality Engineer


Key Responsibilities:

  • Drive and implement process improvements to ensure predictable processes across all product lines (e.g. Risk Reduction, Yield improvements, Customer complaint reduction, Error proofing, Cost Reduction initiatives, Process Automation activities)
  • Provide effective and responsive QA support to Operations to meet their area's objectives of quality, cost and output.
  • Ensure all process variables and their interactions are adequately defined. Ensure all failure modes in process have been identified and addressed. (e.g. Use of DOE studies, FMEA's)
  • Drive and implement plant wide quality system improvements.
  • Ensure Regulatory compliance in area of responsibility to cGMP's of all medical device regulatory agencies (e.g. FDA and TUV)
  • Provide functional expertise to other support functions on quality related issues (e.g. regulatory requirements, statistical techniques, sampling principles).
  • Identification and implementation of appropriate statistical techniques to monitor process performance (e.g. SPC, CpK analysis, sampling techniques)
  • Approval of change requests for product, process and quality system changes.
  • Customer complaints: Analysis of returns, approval of analysis reports and analysis of complaint trends.
  • Validation: Define process and product validation requirements, preparation and approval of Master Validation Plans, protocols and reports approval.
  • Compilation of required Regulatory documentation (e.g.Technical files, Design Dossiers, Product transfer files, Essential requirements)
  • MRB: Review of MRB trends and identification of appropriate corrective actions when required.
  • Perform internal quality audits.
  • Support the implementation of Lean Manufacturing across the site.
  • Transfer and implement product and processes from development or from another manufacturing facility.


    Education, experience and Skills
  • Minimum qualification: BSC/BEng degree.
  • Minimum of 2/3 years experience in a QA role
  • Knowledge of GMP regulated environment and experience in a similar role would be an advantage.
  • Strong project management skills.
  • Good level of technical and analytical expertise to assist in problem solving.
  • Good knowledge of statistics would also be an advantage.


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