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Senior Quality Engineer (Part-time)

Senior Quality Engineer (Part-time)

Job description

Senior Quality Engineer

About Your New Company

This an opportunity with one of Ireland's leading bespoke automation manufacturers. Their main clients are medical device and pharmaceutical multinationals. This is a permanent job and you can work full-time or part-time hours depending on your needs. Based on the nature of work, this person will ideally be onsite. This company works towards ISO 9000 and medical device experience is not essential.

Please note this is an onsite position, no remote working option available.

About Your New Job as a Senior Quality Engineer 

  • Lead and manage the site QMS including Document Control activities, standardization activities, develop systems, reporting of quality trend data, and taking appropriate action.
  • Reviewing and approving documentation required at each stage of the project lifecycle – FDS, SOP’s, Project checklists, BOM’s, User Manual pack etc.
  • Creation of internal test documentation and ensuring all machines are inspected and tested to meet customer requirements.
  • Final review of equipment prior to shipment.
  • Lead projects on all quality related issues and ensuring an effective and robust quality system which complies with all relevant regulatory requirements.
  • Participate and lead investigations (NC / CAPA), involving but not limited to collecting, identifying and analysing information, investigating product and quality problems and identify effective corrective actions.
  • Ensuring training records are maintained to ensure all employees trained on new or changed procedures.
  • To effectively manage and report all Quality Metrics including Production metrics, Non Conformities, Change controls, SOP’s. Ensuring all actions are assigned and tracked to ensure compliance with critical quality KPI’s.
  • Drive the understanding across the company of the cost of quality through Critical To Quality initiatives and Right First Time.

What Skills You Need:

  • Minimum of 6+years' experience in QA/Compliance in a regulated environment.
  • A third level Degree in a related Science or Quality Management discipline.
  • Internal Audit Accreditation would be preferable.
  • Systems and Process thinking 
  • Enthusiasm for collaboration across Departments
  • Excellent communication skills 

What's Next?

Apply for your new job now by clicking the apply button, or contact Emma Ward at Sigmar Recruitment on:

  • T: +353 91 455307
  • E:

..for more information.

All applications will be treated with the strictest of confidence. Sigmar will never forward your CV to a third party without prior consent.