JOB TITLE:
Medical Device Product Builder / Engineering Technician
Exciting opportunity for a Product Builder / Engineering Technician to join a medical device company developing and commercializing a platform interventional technology. The Medical Device Product Builder / Engineering Technician supports the manufacturing, testing, and release of Selio Medical products. This role combines hands-on device assembly with technical inspection, testing, batch release, and process improvement responsibilities to ensure high-quality, compliant product delivery. Working cross-functionally with R&D, Quality, and Operations, the technician contributes to device verification, validation, and production. This role is based in our facility in Dublin 8 and can offer part time or full time working hours.
KEY RESPONSIBILITIES:
* Manufacture and assemble medical device products per specifications and controlled procedures.
* Perform in-process and final testing to support batch release and product acceptance.
* Review and maintain manufacturing and test documentation (MPs, DHRs, TMDs, FMs).
* Support root cause investigations and process improvements using structured problem-solving tools.
* Manage calibration and maintenance schedules for manufacturing and testing equipment.
* Conduct receiving inspections for components and manage inventory of materials and consumables.
* Support process validation and risk management activities (pFMEA, dFMEA).
* Liaise with suppliers and vendors for component orders, calibration, and service tasks.
* Train and support production operators in manufacturing and test procedures.
* Ensure compliance with all company quality and regulatory procedures.
QUALIFICATIONS AND EXPERIENCE:
* ≥3 years experience in medical device or pharmaceutical manufacturing.
* Strong knowledge of manufacturing and testing processes for medical devices.
* Experience with equipment qualification, validation, and documentation.
* Competent in technical writing and data reporting.
* Excellent attention to detail and commitment to quality and compliance.
COMPETENCIES:
* High manual dexterity, attention to detail, and the ability to work efficiently in a quality-controlled manufacturing environment ensuring adherence to all documentation and procedures.
* Understanding of medical device regulatory and quality requirements (ISO 13485, GMP).
* Strong teamwork, communication, and problem-solving skills.
* Ability to work cross-functionally and build effective internal/external relationships.
BENEFITS
* Bring a new medical device to market to benefit patients, clinicians and healthcare systems.
* Work with a passionate experienced team in a fast-moving medical device start-up based in the Guinness Enterprise Centre, a connected innovation hub.
* Fast tracked career progression.
* Excellent remuneration package.