We are delighted to be partnering with an exciting Medical Device company based in Dublin, on a permanent Quality Engineer position.
This role will be a significant contribution to this company in a pivotal stage of their growth and will focus on supporting the execution of the quality management system and represent the quality division cross-functionally including quality support on process development and manufacturing/supply chain projects.
As Quality Engineer, your primary responsibilities will include:
* Quality support with process development and change control across equipment design, process parameters, component control and inspections.
* Use of statistical methods and tools to trend quality metrics and key performance indicators within the QMS.
* Handling of quality events including non-conformances and root cause analysis.
* Preparation and management of all aspects of document control within the QMS according to the requirements of ISO13485.
* Support with Internal and External Audits.
* Engagement with various stakeholders as required including suppliers and regulatory authorities.
Education & Experience Required:
* Bachelor’s Degree in Engineering, Science or related field.
* 2 years in a similar role in QA within the medical device industry.
This is a hybrid role, which will require 3 days per week in the office in Dublin.
Seniority level: Mid-Senior level
Employment type: Full-time
Job function: Quality Assurance, Manufacturing, and Science
Industries: Medical Equipment Manufacturing
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