Job Title
We are currently recruiting for an exciting opportunity with a leading medical device organization in Limerick.
-----------------------------------
About the Role
This is an excellent position for anyone looking to join a multinational company renowned for its expertise in medical devices.
-----------------------------------
Main Responsibilities
* Develop and execute plans to continuously improve product quality and process yield, utilizing process characterization and optimization techniques.
* Identify and implement process-related continuous improvement activities to enhance product quality and Overall Equipment Effectiveness.
* Evaluate all process developments and improvements against Quality Management System requirements (ISO 13485, FDA & JPAL).
* Provide strong leadership and a clear work ethos within the team, collaborating with personnel to address Corrective/Preventative actions for Quality, Technical, and Manufacturing issues.
* Manage projects efficiently, ensuring accurate planning, timely delivery, and comprehensive reporting of project deliverables.
* Promote Behavioural Standards aligned with company policies and procedures.
* Contribute to Environmental and Health & Safety efforts by staying updated on new technologies and presenting Best Practice methodologies to the company.
-----------------------------------
Requirements
* Primary Degree (Level 8) in Process, Production, Manufacturing, Polymer, Materials, Biomedical, or Mechanical engineering, with a minimum of 4 years' experience.
* Relevant experience with statistical process control and capability analysis is required.
* Desirable qualifications include Six Sigma/Green Belt/Black Belt accreditation.
* Strong analytical and problem-solving skills, with proficiency in root cause analysis and risk assessments.
* Familiarity with manufacturing and validation in regulated environments (FDA or IMB) is advantageous.