Save Job Back to Search Job Description Summary Similar JobsDrive quality excellence in a growing medical technology environmentLead process improvements and influence cross‑functional decisionsAbout Our ClientOur client is a global medical technology manufacturer known for delivering high‑precision products used in healthcare settings worldwide. They are expanding their quality function and seeking experienced professionals who can elevate operational standards and support long‑term growth.Job DescriptionOversee quality management systems and ensure strong regulatory compliance across manufacturing operationsDevelop, implement, and maintain quality assurance procedures aligned with FDA, ISO 13485, and other relevant standardsSupport both internal and external audits, ensuring all documentation and processes meet compliance requirementsMonitor production processes to identify quality gaps and resolve issues proactivelyConduct product investigations, lead root‑cause analysis, and implement effective corrective and preventive actions (CAPA)Support new product transfers by ensuring quality requirements are built into early development and production phasesLead validation activities including IQ, OQ, PQ, process validation, and test method validationDrive continuous improvement initiatives to enhance product quality and operational efficiencyManage customer feedback and complaints, ensuring timely resolution of quality‑related concernsCommunicate any necessary process changes or updates to customers and internal teamsProvide technical guidance and quality‑related support to internal and external stakeholdersMaintain accurate quality documentation, inspection records, and monthly/annual quality reportsTrain manufacturing personnel on quality procedures, standards, and best practicesPromote a strong culture of compliance, quality ownership, and continuous improvementThe Successful ApplicantA degree in Engineering or Science, Diploma holders with extensive experienceQuality experience, preferably in medical devicesStrong knowledge of FDA regulations and ISO 13485Strong analytical and problem‑solving skills with a structured approach to troubleshootingAbility to collaborate effectively with cross‑functional teams and communicate clearlyExperience working in cleanroom or controlled environments is an advantageWhat's on OfferOpportunity to drive quality excellence in a regulated and fast‑growing sectorExposure to new product transfer projects and key validation activitiesCollaborative work culture and cross‑functional project involvementCareer growth in an established, innovation‑driven medical technology organisationContactVanessa Chan (Lic No: R2197577/ EA no: 18S9099)Quote job refJN-032026-6959737Phone number+65 6643 9742Job summaryFunctionHealthcareSpecialisationHealthcareWhat is your area of specialisation?Industrial / ManufacturingLocationSingaporeContract TypePermanentConsultant nameVanessa Chan (Lic No: R2197577/ EA no: 18S9099)Consultant contact+65 6643 9742Job ReferenceJN-032026-6959737
