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Quality Engineer

Location: Limerick
Experience:2-3 Years
Job Type:Fixed Term Contract
Salary:Not Disclosed
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May be suitable for: EHS Engineer, Quality Engineer

Quality Engineer

Provides leadership and support to Water Room and Formulations process, and ensures good Quality Engineering practices are in use. Drives continuous improvement through data driven approaches and monitoring of quality systems.

Job Responsibilities:

  • Provides complex product team support for quality system design and audit, compliance assessment, and for support of steady state manufacturing processes
  • Utilizes multifaceted industry and process excellence standards on an expert level in daily quality operations, including good manufacturing practices (GMP), equipment engineering system (EES), and international organization for standardization (ISO).
  • Addresses and corrects product and process complaints.
  • Ensures comprehensive measurement systems to monitor effectiveness of quality and reliability systems to identify, bracket, correct and prevent defects, presenting reports to management
  • Responsible for supporting the activities of Operations/Engineering/information management in building quality into our products and assuring compliance to the pertinent regulations while at the same time attaining operational effectiveness
  • Leads and executes upgrades to Quality System
  • Support QA programs in assuring compliance to the pertinent regulation
  • Identify and lead cost and technical improvements under the departments’ continuous improvement program.
  • Provide key inputs and leadership into transformational process developments.
  • Project Management - provide timely and accurate reporting on project activities.
  • New Product Introductions & Product Transfers
  • Lead or actively participate in cross-functional teams to ensure New Product Introduction/Research and Development projects are completed in a timely and efficient manner.

Education and Experience Required for Role Essential:

Degree Qualified with 3-5 years relevant experience in Medical Devices/Pharmaceutical Industry Ability to work on own initiative Flexible work ethic Attention to detail CAPA and RCI experience Excellent IT skill eg , experience in minitab , excel reports Desirable Risk management experience Automated process controls experience Good presentation skills Responsibilities and accountabilities will vary for all positions and the scope of individual roles may not be limited to the contents of this position description. QUMAS procedures will define responsibilities from time to time and each manager is responsible for complying with these processes, which supplant any responsibility outlined within. As such, adherence to company procedures is also a responsibility of this role.

For more information contact Paul O'Brien in the strictest of confidence.

If you would like further Information you can contact the recruiter directly:

Paul O'Brien | Tel: +353 (0) 212 339 370


Under the Data Protection Acts 1988 and 2003, your details will be kept confidential and will not be passed to a third party without your express prior consent.

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