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Quality/Manufacturing Engineer
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Galway, Galway, Ireland Oxford Global Resources Full timeOverviewJoin to apply for the Quality/Manufacturing Engineer role at Oxford Global Resources.Are you a Quality/Manufacturing engineer looking for a new opportunity? Don\'t hesitate and apply todayProject descriptionWe are seeking experienced Remediation Quality Engineers / Manufacturing Engineers to support a site-wide remediation program following an FDA...
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Galway, Galway, Ireland Oxford Global Resources Full timeManufacturing/Quality Engineer – Oxford Global ResourcesOverviewTechnical Recruiter at Oxford International is seeking a Quality/Manufacturing Engineer for a site-wide remediation program following an FDA 483. The role focuses on manufacturing process validation, quality system updates, and documentation remediation. Consultants will work onsite with...
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Manufacturing Engineer
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Galway, Galway, Ireland Oxford Global Resources Full timeAre you interested in taking the next step in your career with a global leader in the medical device industry? Are you ready to challenge yourself in a fast-paced and high-regulated environment? Are you an experienced quality or manufacturing engineer? You could be the perfect candidate for this opportunity Don't hesitate, apply today Job Description Our...
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Manufacturing Engineer
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Galway, Galway, Ireland Oxford Global Resources Full timeAre you a manufacturing engineer looking to progress your career?Are you interested in taking the next step in your professional journey with a global leader in the medical device industry?Are you ready to challenge yourself in a fast-paced and high-regulated environment?You could be the perfect candidate for this opportunityDon't hesitate, apply todayJob...
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Manufacturing Engineer
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Galway, Galway, Ireland Oxford Global Resources Full timeAre you a manufacturing engineer looking to progress your career? Are you interested in taking the next step in your professional journey with a global leader in the medical device industry? Are you ready to challenge yourself in a fast-paced and high-regulated environment? You could be the perfect candidate for this opportunity Don't hesitate, apply...
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Galway, Galway, Ireland TE Connectivity Full timeJoin to apply for the Manufacturing Engineer role at TE Connectivity.OverviewThe Manufacturing Engineer in a sustaining role focuses on maintaining and improving existing manufacturing processes to ensure consistent production of high-quality medical devices. This role is integral to troubleshooting issues, implementing process improvements, and supporting...
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Manufacturing Engineer
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Galway, Galway, Ireland Oxford Global Resources Full timeOverviewAre you a manufacturing engineer looking to progress your career? Are you interested in taking the next step in your professional journey with a global leader in the medical device industry? Are you ready to challenge yourself in a fast-paced and high-regulated environment? You could be the perfect candidate for this opportunity Don\'t hesitate,...

Quality/manufacturing engineer
3 weeks ago
Are you a Quality/Manufacturing engineer looking for a new opportunity? Don't hesitate and apply today PROJECT DESCRIPTION We are seeking experienced Remediation Quality Engineers / Manufacturing Engineers to support a site-wide remediation program following an FDA 483. These roles will focus on manufacturing process validation, quality system updates, and documentation remediation. Consultants will be based onsite and work directly with manufacturing and quality process owners to identify compliance gaps, implement corrective actions, and ensure documentation is accurate and audit-ready. The project will involve tackling remediation areas in sequence, updating technical files and procedures, and ensuring robust validation of manufacturing processes. Consultants must be able to take a problem statement through to a compliant solution, collaborating cross-functionally across Quality, Manufacturing, and Regulatory teams. PROJECT DESCRIPTIONPartner with process owners on the floor to capture and remediate issues.Support process validation (IQ/OQ/PQ) and documentation updates.Drive CAPA/NCR closure and implement compliant solutions.Provide technical writing for quality and manufacturing documents.Collaborate cross-functionally to ensure regulatory compliance. CONSULTANT RESPONSIBILITIESEngineering or Quality degree with 5-10 years' med-tech experience.Background in remediation, process validation, CAPA, NCRs.Strong technical writing and documentation skills.Knowledge of 21 CFR Part 820, ISO 13485.