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Process engineer / manufacturing

Cork
Oxford Global Resources
Process engineer
Posted: 15 September
Offer description

Are you a process or 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 familiar with remediation tasks? 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 today! Job Description Our client in Cork require experienced Process Engineers to support an upcoming project. This role will focus on manufacturing process validation, quality system updates, and documentation remediation. You 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. Key ResponsibilitiesAnalyse process, product, material or equipment specifications and performance requirementsUnder broad supervision / guidance compile and analyse operational, test and experimental data to establish performance standards for newly implemented or modified products / processesSummarise, analyse and draw conclusions from test results leading to effective technical resolutionTroubleshoot new products / process working closely with product developmentContinually seek to drive / improvements in process design, layout and operational performanceDemonstrate good working knowledge and application of validation techniques and associated regulatory requirementsActively promotes and participates in a cross -functional teamwork environmentEvaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effectsUnderstands and comply with all the regulations governing the quality systems Key RequirementsEngineering or Quality degree with 2-3 years' relevant industry experienceBackground in remediation, process validation, CAPA, NCRs.Strong technical writing and documentation skills.Knowledge of 21 CFR Part 820, ISO 13485. BenefitsCompetitive and attractive employee compensation packagePension contributionsHealth insurancePaid public holidays Location: Cork, Ireland | onsite

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