Summary: The Quality Technician performs factory acceptance testing, inspection, and product rework on EMA medical devices and cosmetic products, ensuring compliance with quality and regulatory standards. Highlights: 1. Perform factory acceptance testing and inspection activities 2. Engage in device rework, customization, and quality operations 3. Maintain accurate documentation and ensure compliance with QMS **Company Description** EMA Aesthetics Ltd. is an Irish company (established in 2019\) specialising in medical and aesthetic devices, as well as professional skincare products. Our portfolio is marketed globally under the Préime brand—derived from the Irish *“Préimhe,”* meaning *premium*. Our flagship product lines include Préime DermaFacial, Préime DermaCeuticals, and Préime DermaProfessional. We pride ourselves on the efficacy of our offerings and have secured leading intellectual property in both device technology and regenerative therapies. Our approach emphasises Combination Therapy, enhancing the utility of our products either as standalone treatments or in conjunction with other aesthetic procedures. Our channels to market include both sub\-distributors and direct sales operations, supplying clinics, medspas, doctors, and skincare professionals. Since our inception, we have formed strategic partnerships with Sinclair Pharmaceuticals, Merz Aesthetics, and Rohto Pharmaceuticals. Our global distribution footprint spans 60\+ countries, supported by subsidiaries in Belgium, Dubai, and the United States. **Position Title** Quality Technician **Function** Quality Control, Factory Acceptance Testing (FAT), and Rework Operations **Position Overview** The Quality Technician is responsible for performing factory acceptance testing, inspection, and product rework activities on EMA medical devices and cosmetic products at manufacturing and warehouse facilities. This role ensures all units meet EMA cosmetic, functional, and regulatory requirements before release to stock and shipment. The Specialist is also responsible for maintaining traceability, completing inspection reports, and providing documented feedback under EMA Quality Management System (QMS) procedures. This position requires strong attention to detail, technical capability, and strict adherence to defined work instructions and acceptance criteria. **Key Responsibilities** **1\. Factory Acceptance Testing (FAT) – Sabadell Factory** Perform factory commissioning tests and inspection activities, including: * Functional and cosmetic inspection * Inspect devices against cosmetic acceptance criteria * Verify assembly integrity (screws, connectors, mechanical parts) * Check screen condition, alignment, and finish * Verify labeling, serial numbers, QR codes, and traceability * Performance testing * Device configuration and final validation * Verify device documentation * Confirm firmware and traceability alignment * Capture required photographic documentation **2\. Device Rework, Customization \& Quality Operations – Vallirana Warehouse** * Device handling and rework * Unpacking and preparation of devices * Installation of protective components * Label replacement and application * Power cable replacement and configuration * Component allocation and stock assignment * Visual inspection and documentation * Take photos of device, labels, and packaging * Complete rework checklists and inspection reports * Upload documentation to EMA systems * Report non\-conformities and deviations **3\. Reporting and Documentation** Maintain accurate and complete records of: * FAT reports * Inspection checklists * Rework documentation * Traceability information * Non\-conformance reports Ensure all documentation complies with EMA Quality Management System and ISO 13485 requirements. **4\. Coordination and Communication** * Communicate inspection results to EMA technical and quality teams * Escalate quality issues when required * Coordinate with warehouse and factory personnel * Ensure proper handling and traceability of devices **5\. Rework Operations – Cosmetic Products (Vallirana Warehouse)** Support and supervise post\-production and customization activities on EMA products (DermaFacial consumables, Dermaceutical, and Dermaprofessional products). **Responsibilities include:** * Relabeling operations * Regulatory labels * Language localization * Market\-specific compliance (EU / Middle East / International) * Product rework * Repackaging * Kit reconfiguration * Correction of labeling/packaging deviations * Variable printing operations * Lot number * Manufacturing date (MFD) * Expiry date (EXP) * Traceability codes * Packaging customization * Shrink wrapping * Tamper\-evident seals * Market\-specific packaging modifications * Operational supervision * Coordinate temporary operators or warehouse staff * Ensure correct execution of work instructions * Validate finished goods before release * Equipment operation and maintenance * Label printers * Coding printers * Shrink wrapping equipment * Ensure setup and calibration * Coordinate maintenance/troubleshooting * Train temporary staff **Key Performance Indicators (KPIs)** * FAT completion rate * Inspection accuracy * Documentation completeness * Non\-conformity detection effectiveness * Rework quality and compliance * Turnaround time per device **Experience \& Requirements** * Experience in quality control, inspection, or production environments * Strong attention to detail * Ability to follow structured procedures and work instructions * Ability to perform basic technical testing * Ability to complete reports and documentation * Experience with product rework or post\-production operations * Basic understanding of cosmetic labeling systems and traceability printing * Ability to operate light packaging or coding equipment * Ability to supervise temporary operators or warehouse staff Job Type: Full\-time Application Question(s): * Do you currently live in Spain? * Are you confortable working under a consultancy agreement (freelancer)? Language: * English (Required) Work Location: In person