Quality Engineer I â Medical Devices
Quality Engineer I â Medical Devices
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Job Description
Job description
Location: Galway (On-site)
Industry: Medical Device / Start-up
Our client a dynamic and fast-paced medical device start-up based in Galway is seeking a Quality Engineer I to join their growing team. The company is focused on developing innovative patient-centric technologies to improve quality of life and is advancing rapidly through the product development lifecycle toward global market launch.
This role offers a unique opportunity for a motivated and hands-on quality professional to apply their engineering knowledge across multiple areas of a developing Quality Management System. The ideal candidate will enjoy working in a cross-functional start-up environment and contributing directly to impactful product development.
Responsibilities include but are not limited to the following:
Apply quality engineering expertise across the Quality Management System (QMS).
Support certification and maintenance of compliance to ISO 13485 and 21 CFR Part 820.
Assist with design assurance activities including design controls verification and validation.
Support development and validation of test methods and computer system assurance programs.
Participate in risk management and usability engineering activities.
Maintain document control through QT9 eQMS and perform related administrative tasks.
Contribute to the CAPA and non-conformance (NC) investigation and resolution process.
Assist in internal and external audits and implement corrective actions as needed.
Support updates and gap assessments for applicable regulatory standards and guidance.
Participate in supplier quality management vendor evaluation and AVL maintenance.
Collaborate cross-functionally to uphold quality objectives and continuous improvement.
Perform additional quality-related duties to support business goals and KPIs.
Job requirements
Bachelors degree in engineering science or related field (or equivalent).
Minimum of 2 years experience in a medical device or supplier environment.
Familiarity with ISO 13485 FDA QSR (21 CFR Part 820) and GMP requirements.
Experience in both FDA and European regulatory environments is preferred.
Strong initiative problem-solving and follow-through in executing responsibilities.
Understanding of risk management methodologies (ISO 14971).
Experience with sterilization (EtO/Gamma) biocompatibility and transportation testing is a plus.
Prior involvement in audits or inspections is an advantage.
Proficiency in MS Office and familiarity with electronic QMS tools.
Immediate interviews available for suitable candidates.
Note: By applying for this position you may also be considered by Pale Blue Dot Recruitment for other future vacancies
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Employment Type
Full Time
