We are seeking a motivated and detail-oriented Production Operator to join our growing manufacturing team in Swords, Dublin. This is an excellent opportunity for someone with experience in regulated manufacturing environments who is passionate about quality, compliance, and operational excellence.The Production Operator will play a key role in the preparation, mixing, packaging, and labelling of chemical reagents, ensuring the highest standards of quality, safety, and regulatory compliance are consistently maintained.The Ideal CandidateThe successful candidate should have:A minimum of 1 year’s experience within a medical device, IVD (In‑Vitro Diagnostics), pharmaceutical, or chemical manufacturing environmentPrevious experience working within medical companies or organisations involved in IVD product manufacturing is highly advantageousA strong understanding and practical application of Good Manufacturing Practices (GMP)Proficiency in Microsoft Office applications for documentation and reporting purposesExcellent communication and interpersonal skills, with the ability to collaborate effectively within a team environmentThe ability to work independently with minimal supervision while maintaining high standards of quality and accuracyA proactive and accountable approach to work, with the ability to take ownership of tasks and contribute effectively to team responsibilitiesPrevious Quality Control or laboratory experience within a regulated environment would be advantageousA third‑level qualification in Quality, Engineering, Materials Science, Mechanical Engineering, Instrumentation, or a related discipline would be beneficialKey ResponsibilitiesExecute manufacturing and packaging operations to ensure the consistent production of high‑quality productsHandle production materials and chemicals, including storing, retrieving, mixing, and monitoring chemicals used throughout the manufacturing processEnsure full compliance with Quality Management System (QMS) procedures, GMP requirements, and all associated manufacturing documentationOperate, monitor, and troubleshoot production equipment and processes to maintain efficiency and product qualityAccurately record production data, including ingredients, weights, temperatures, and in‑process inspection results, and input information into relevant systems and databasesCollaborate with cross‑functional teams to support efficient production workflows and achieve operational targetsAssist in the preparation and maintenance of QMS documentation, including Standard Operating Procedures (SOPs) and validation documentationComplete all required training related to manufacturing processes, product handling, and shipment proceduresMaintain high standards of GMP compliance, cleanliness, and housekeeping across manufacturing areasEnsure adherence to all Environmental, Health & Safety (EHS) policies and company proceduresCarry out any additional duties assigned by the immediate supervisor to support operational requirementsWhy Join Us?Opportunity to work in a highly regulated and innovative manufacturing environmentOpportunity to work with a collaborative and international teamBe part of a company committed to quality, safety, and continuous improvement
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