Graduate Quality Engineer
About Your New Employer
Start-up medical device company based in Galway. This is a permanent job - please note, we are unable to provide visa sponsorship at this time.
About Your New Job
Liaise with technical operations to support inspection and manufacturing activities, ensuring consistent delivery of compliant products.
Develop and implement inspection procedures for incoming components, in-process assemblies, and final products; manage and coordinate all inspection activities.
Manage the Equipment Management System and oversee product configuration for Clinical Investigations, including product distribution and returns in line with quality system procedures.
Complete quality system documentation, assist with document control, and review Device History Records (DHR) to prepare product release documentation.
Prepare quality system metrics for management meetings and reviews, and support continuous improvement of quality system processes.
Complete additional tasks as designated by your supervisor to support business needs.
What Skills You Need
Bachelor’s degree in Science or Engineering (required).
Minimum of 1 year’s experience in a quality engineering role, medical device industry experience is essential.
Strong self-starter with the ability to work independently and proactively advance company goals.
Excellent written, interpersonal, and presentation skills.
Demonstrated accountability, ownership, and reliability in meeting commitments.
Ability to travel domestically and internationally; valid driver’s license and passport required.
Willingness to continuously develop skills and stay current with relevant standards and regulations.
What’s Next
Apply now by submitting your CV and cover letter. If you’re passionate about quality in medical device operations and want to be part of a team making a difference in healthcare, we want to hear from you! If this role isn’t quite right but you’re interested in similar opportunities, please get in touch – we have multiple roles available in quality and regulatory affairs.
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