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Job ID: JOB-13572

Quality Engineer –  Initial 24 month FTC

Working in Quality is in big demand right now.  We’re looking to speak with experienced Quality Engineers who are looking to work with top global leaders who value their people.  This is a great job opportunity in Athlone for a Quality Engineer who enjoys working on innovative projects, values autonomy in their job and  working in a great team.

Our client focus’ on the development of cutting-edge medical devices in Airway Management but also for other life enhancing applications. 

Key Responsibilities:

• Develops, modifies, applies, and maintains quality standards and protocols for processing materials into partially finished or finished materials product.
• Collaborates with engineering and manufacturing to ensure quality standards are in place.
• Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
• Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
• Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
• Participate in preparing / critically reviewing/approving NCMRs/ CAPAs/ Investigations and validation activities, providing expert QA technical direction and solutions as appropriate.
• Ensures effective product control measures in the event of issues being noted.
• Establishes the quality and compliance requirements for new manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling, fabrication of tools and equipment.
• Interacts with internal and external stakeholders in the processing of all quality and compliance activities and documentation ensuring our right-first-time culture prevails.
• Leads quality compliance activities including structuring and writing of protocols and reports for design, FAT, SAT, IQ, OQ, PQs in compliance with FDA CFR 21 part 11 and other relevant parts.

Qualifications – Key Skills & Experience

• Level 8 or higher qualification in Engineering /Science discipline with a minimum of 3 years of relevant experience in a highly regulated environment.
• Requires broad knowledge of manufacturing processes and quality systems, techniques and practices typically gained through extensive experience and/or education.
• Experience with DFA (Design for Automation), GAMP5, Lean Sigma, Minitab.
• A dynamic team player and problem solver who can work effectively on cross-functional teams

For further information on this role in please contact Mark Wilson on 0860449473 or email talent@hero.ie

Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/

Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.

Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given.  You have supplied us with your personal data in the process of applying for a position.  Our client company may have personnel outside of the EEA who will review you data.  We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

Mark Wilson

JOB-13572

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