Quality jobs in GavàCreate job alerts

iVascular is a fast growing company founded in 2010 in Barcelona (Spain) with the aim of developing medical devices and therapies for the treatment of disorders of the vascular system and to become a reference in the vascular field by enhancing the value of technology and innovation. The team that started iVascular has more than 30 years of experience in the field of vascular devices, being responsible for obtaining one of the first CE marks for a drug-eluting stent more than 20 years ago. We are currently looking for an R&D PROJECT LEADER for our plant located in Sant Vicenç dels Horts (Barcelona). Your main objective will be to lead the development of a delivery system for a medical device, from 2D/3D prototype design to the management of prototype manufacturing, coordination of bench testing, analysis of results and report writing, leading the device verification phase, and preparing the necessary documentation for submission to regulatory authorities. KEY RESPONSIBILITIES: • Prepare the technical planning for assigned projects, applying the methodology implemented in the company., • In collaboration with the department head, prepare project budgets and define the technical and human resources to achieve the technical and economic objectives., • Ensure the feasibility and technical quality of the solutions proposed., • Coordinate and implement the production process for the products developed., • Research and develop improvements in the technical characteristics, quality, and costs of products., • Define purchasing specifications and approve suppliers from the initial stage until the product is transferred to the factory, sending guidelines for subsequent procurement. DESIRED PROFILE: • Industrial Engineering, especially in the mechanical, electromechanical, materials, biomedical fields or a similar one., • High level of English and Spanish., • Minimum 5 years of experience in a similar position., • Previous experience working in an R&D department. Previous experience working with CAD systems (especially Solidworks and Rhinoceros) and Ansys., • High capacity for multidisciplinary work, analytical capacity, integrity, cooperative spirit, communication skills. Innovative sense, high self-esteem, and high expectations for professional development. WHAT WE OFFER: • Permanent contract, stable position within a high-impact strategic project at a company currently expanding internationally and with global reach., • Competitive salary based on experience, plus attractive benefits., • Real growth opportunities in a flexible, collaborative, multidisciplinary, young and dynamic environment., • Flexible compensation (restaurant tickets, transportation, and childcare)., • iWellness service: physiotherapy, gym and cycling club., • Corporate events and gifts., • Company-owned cafeteria., • Work-life balance.

Actual Talent is the talent acquisition consultancy that offers Executive Search, RPO and Talent Solutions. Our purpose is to drive the growth and fulfillment of individuals and organizations. We facilitate individuals in finding inspiring opportunities and help organizations discover professionals who will take them to the next level. We do this through talent acquisition and development solutions that focus on people, diversity and inclusion, innovation, and cutting-edge technology. About the client: We are seeking a Supply Chain Specialist - Medical Devices to join one of our clients in the pharmaceutical sector. The position is based in Barcelona and offers a hybrid work model. Your mission: The Supply Chain Specialist for Medical Devices will establish, optimize, and execute supply chain operations for the digital medical devices portfolio in our client therapeutic area. This role is pivotal as it involves building a supply chain framework from scratch within a regulated, innovative business environment, ensuring timely and compliant availability of digital devices to support patient treatment. Your major accountabilities: ✔ Set up and manage the end-to-end supply chain for digital medical devices in the CNS area, including procurement, demand planning, inventory, vendor management, and distribution, adhering to medical device regulations (ISO 13485, EU MDR, FDA). ✔ Coordinating the Medical devices S&OP process, the short, medium and long-term planning process, translating demand, into an optimal production schedule for Contract Manufacturing Organizations. ✔ Monitor inventory levels at affiliate locations and ensure adherence to inventory targets in close collaboration suppliers. ✔ Exception-based management of operational supply issues, such as out-of-stock events, support the prioritization and allocation in supply bottleneck situations and recall scenarios with agility, prioritizing compliance and patient safety ✔ Responsible for routine reporting on area KPIs along with appropriate analysis and countermeasures where necessary. ✔ Continuous process and performance improvement: Systematically review and optimize supply chain processes for efficiency and scalability. We would like you to have: • Minimum 5 years of experience as a Supply Chain Specialist / Logistics with recent experience in medical devices (digital health/connected devices)., • Bachelor’s degree in engineering, business or a comparable degree., • In-depth knowledge of ISO 13485 and EU MDR; strong understanding of quality and audit processes (CAPA, traceability, documentation), • Strong sense of time organization and urgency, analytical thinking with a high degree of initiative and problem-solving skills. Able to work independently., • Fluent in English., • Strong command of SAP Supply Chain Management., • Good knowledge in MS Office Suite, PowerBI, basic programming skills in VBA, Python or similar preferred., • Analytical Thinking, problem solving, communication and initiative skills. Ideal Experience: • Experience in start-up/greenfield medical device operations, • Quick learner with the ability to handle multiple tasks simultaneously, maintain focus, and adapt to a variety of challenges. Ability to conduct detailed procedures in a time-constrained environment.

Del Monte is an international Group offering a variety of wholesome and nutritious products essential to a healthy lifestyle. It is one of the world's leading vertically integrated producers, marketers and distributors of high-quality fresh and fresh-cut fruits and vegetables, as well as leading producer and distributor of prepared fruits and vegetables, juices, beverages and snacks in Europe, Africa and the Middle East. The Group is established in more than 100 countries and has nearly 40,000 employees worldwide. We are looking for an Accountant for a permanent position based in Castelldefels, Barcelona, Spain. Reporting to the Senior Financial Manager, the successful candidate will be responsible for: • Oversee financial operations, ensuring accurate reporting and compliance with regulations., • Prepare and analyze financial statements, budgets, and cash flow projections., • Manage transactions with financial institutions and review bank reconciliations., • Ensure timely preparation of donor reports and financial statements., • Maintain the fixed asset register and prepare annual asset reports., • Collaborate with auditors during audit processes., • Implement financial policies and procedures to enhance efficiency., • Match AP invoices with PO’s., • Book AP invoices., • AR invoicing monitoring AR ageing reports., • Statutory accounting subsidiary, complete accounting and tax reporting, VAT, income tax, payments, invoicing, collections, Bank., • Filing. Required skills and competencies: • Minimum 2-3 years overall experience., • Degree in accounting (Licenciatura Economicas o Empresariales), • Proficiency in Excel and ERP systems., • Fluent in written and spoken English, Spanish appreciated., • Organizational maturity and effectiveness., • Able to demonstrate professional competence, both within the company and with external contacts., • Results orientated with a positive approach., • Ability to deal with change., • Excellent Communication Skills / Proficiency in Computers., • Able to maintain performance and focus in demanding situations.

¿Quieres unirte a un grupo innovador y en crecimiento? ¡Únete a Flex-N-Gate!⚡ Flex-N-Gate es un proveedor mundial líder e innovador de sistemas de automoción. Brindamos soluciones únicas y flexibles a través de nuestros 75 centros de producción e I+D alrededor del mundo ofreciendo a nuestros clientes calidad, eficiencia, control y optimización de costes. Actualmente empleamos a más de 27.000 personas en todo el mundo en diferentes líneas de negocio plásticos, metales, conjuntos mecánicos y sistemas de iluminación. El/la Quality Engineer apoya y promueve los esfuerzos de mejora de la calidad de la planta y coordina la acción correctiva y la mejora continua. Es responsable del aseguramiento de la calidad del producto y del proceso desde su liberación (PPAP), y durante la vida del producto. Trabajará en un equipo altamente enfocado a la calidad, y mantendrá contacto con las distintas áreas de la empresa, los proveedores y clientes para asegurar que los productos fabricados cumplan o superen los requisitos del cliente y de la planta. Responsabilidades • Mantenimiento de la calidad del producto y del proceso en serie., • Participación en el mantenimiento del sistema de calidad (documentación de Proceso, etc), • Representación de la empresa ante el cliente y Reportes 8D., • Gestión de las no Conformidades Internas y Externas, liderazgo en la implementación de las acciones correctivas y de mejora., • Responsable de coordinarse con los departamentos externos (OEM’s, TIER1) e internos de clientes (Dptos. de desarrollo y producción de procesos). Requisitos • Estudios Ingeniería Industrial mecánica., • Experiencia mínima de 3 años en el sector de la automoción o similar como Quality Engineer, gestionando proyectos y validación de productos y procesos., • Conocimientos Imprescindible conocimientos de los procesos de montaje y estampación y valorable de soldadura de metales. Conocimientos/uso de herramientas de calidad (Proceso FMEA, Planes de control 8D, 5 porqués, Ishikawa) y metrología., • Conocimiento en la realización del seguimiento de los hitos de los proyectos, APQP, PPAP Comprensión de planos, especificaciones de clientes, informes dimensionales y estudios de capacidad., • Idiomas imprescindible nivel alto de inglés, valorable alemán. Soft skills • Persona proactiva con capacidad de trabajo en equipo y adaptabilidad al cambio., • Capacidad de análisis y rigurosidad en la gestión de datos., • Capacidad de generar soluciones creativas., • Capacidad de síntesis, habilidades comunicativas y de liderazgo., • Capacidad para interactuar y representar a la compañía ante clientes y proveedores ¿Qué ofrecemos? • Contrato indefinido a jornada completa, • Proyecto estable con posibilidades de desarrollo, • Horario Flexible, • Paquete retributivo atractivo a convenir según experiencia. (Plan de Retribución flexible)

WE ARE HIRING! HR CONTROLLING INTERN Neuraxpharm is looking for people who want to make a difference and improve patients’ lives within the CNS area. We want individuals who will go the extra mile and make great things happen. Being part of this team does not mean you are just working for a company, but for a cause! Neuraxpharm is looking for a HR Controller Intern based in Barcelona (hybrid role) Your mission: Reporting to the HR Controlling Intern and supporting both the Corporate and Local HR functions, you will be responsible for optimizing the efficiency of the Human Resources function. You will take part in the digital transformation of HR, as well as in the design and implementation of new processes for the Group’s HR function. Your major accountabilities: • Support in analyses/studies on labour matters., • Ensure accurate employee data entry in the HRIS (SuccessFactors): compensation, personal information, organizational data…, • Participate in audits and data quality checks to ensure accuracy and consistency., • Support Compensation & Benefits projects (participate in defining objectives, scales, goal achievement calculations, merit increase processes, job category reviews, etc)., • Assist in preparing HR reports and dashboards for internal stakeholders., • Support internal audits and reporting related to labour relations metrics and compliance., • Support Coordination of personnel planning., • Support in monthly monitoring and analyse variances in FTE, headcount, and personnel costs versus budget and actuals., • Prepare data for financial audits, non financial audits, ESG reports, surveys, etc, • Collaborate with cross-functional teams to improve HR processes and workflows, aiming to automate and streamline workflows., • Participate in coordination of cross-functional HR projects., • Provide general administrative support to the HR team as needed to support smooth and efficient HR services across the organization. We would like you to have: • Currently pursuing a degree in Human Resources-Labour relations, Business Administration, Psychology, or a related field and/or Master degree with the possibility of an internship relation., • Detail oriented., • Able to manage different projects at the same time, eager to learn and contribute., • Energetic and collaborative., • Eagerness to learn and contribute in a fast-paced environment. HR motivation., • Proficient in Microsoft Office Suite (Excel, Word, PowerPoint)., • Fluent in English and Spanish., • It is mandatory to have the possibility to sign a 6-12 months internship agreement. ABOUT NEURAXPHARM Neuraxpharm is a leading European specialty pharmaceutical company focused on the treatment of the central nervous system (CNS), including both psychiatric and neurological disorders. It has a unique understanding of the CNS market built over 35 years. Neuraxpharm is constantly innovating, with new products and solutions to address unmet patient needs and is expanding its portfolio through its pipeline and acquisitions. The company has c. 1,000 employees and develops and commercializes CNS products through a direct presence in more than 20 countries in Europe, two in Latin America, one in the Middle East and globally via partners in more than 50 countries. Neuraxpharm is backed by funds advised by Permira. Neuraxpharm manufactures many of its pharmaceutical products at Neuraxpharm Pharmaceuticals (formerly Laboratories Lesvi) in Spain. Be part of the team where you can count on us to deliver: • Individual Professional development in a leading European pharmaceutical company with an ambitious international growth strategy., • Attractive remuneration according to the experience and skills provided., • An inspiring leadership team that drives performance., • An inclusive culture promoting diversity across the teams that will inspire you every day with a passionate, a dynamic, a result focused and an expert&excellent team!

Del Monte is an international Group offering a variety of wholesome and nutritious products essential to a healthy lifestyle. It is one of the world's leading vertically integrated producers, marketers and distributors of high-quality fresh and fresh-cut fruits and vegetables, as well as leading producer and distributor of prepared fruits and vegetables, juices, beverages and snacks in Europe, Africa and the Middle East. The Group is established in more than 100 countries and has nearly 40,000 employees worldwide. Reporting to Senior Financial Manager, the successful candidate will have to assist the Senior Financial Manager in various missions: • Help finance in all admin task, especially during closing, • To ensure that invoices and costs related are properly introduced and allocated into the system ., • Treasury control, bank booking and reconciliation, • Collections, • Control FA , tagging all assets and balancing with accounting, • Help finance manager in all accounting matters, • Control insurances with corporate, • Liquidate fruit on time and with proper costing Skills and Qualifications: • Minimum 1 year overall experience in Accounting, • Degree in accounting (Licenciatura Economicas o Empresariales), • Proficiency in Excel, • Fluent in written and spoken English and Spanish, Portuguese appreciated., • Organizational maturity and effectiveness., • Able to demonstrate professional competence, both within the company and with external contacts., • Results orientated with a positive approach., • Ability to deal with change, • Excellent Communication Skills / Proficiency in Computers

ICFO is a leading research center in the field of photonics, dedicated to advancing the science and technology of light and its applications. Located in the Mediterranean Technology Park in the metropolitan area of Barcelona, ICFO is at the forefront of groundbreaking research and innovation in areas such as quantum technologies, biophotonics, clean tech, and photonic integrated circuits. ICFO employs 500 people, including researchers, PhD students and staff personnel. In its area of specialization and category, the institute is consistently ranked among the highest-quality research institutions worldwide. Our mission is to contribute to scientific knowledge, foster technology transfer, educate graduate students and postdoctoral researchers, and promote the responsible engagement of science in society. POSITION OVERVIEW As part of the PICs@ICFO Strategic Initiative, ICFO coordinates PIXEurope, a flagship Pilot Line funded under the European Chips JU program. With €400 million in investments and a consortium of 20 partners across 11 countries, the project aims to reinforce Europe's strategic autonomy in photonic technologies and accelerate industrial uptake of cutting-edge integrated photonics. Over the next decade, PIXEurope will enable the transfer of advanced technologies to manufacturing environments, while fostering innovation and scalability across the European photonics ecosystem. We are seeking a Financial Project Manager to join our team and play a key role in the strategic initiative PICs@ICFO. The selected candidate will ensure effective financial management of research projects, including economic monitoring and accurate financial reporting in compliance with applicable funding regulations and ICFO’s internal policies. KEY RESPONSIBILITIES • Overseeing the economic monitoring of the projects that make up the PICs strategic initiative, ensuring their financial sustainability and compliance., • Providing financial guidance to Pilot line Director assisting him in the economic management of their projects., • Preparing financial reports and economic justifications in compliance with applicable regulations and ICFO policies. Ensuring the timely and accurate submission., • Planning and preparing internal and external audits., • Collaborating with the scientific reporting team to align financial and research related aspects of projects. QUALIFICATIONS AND EXPERIENCE REQUIRED • A university degree in Economics, Business Administration, or a related discipline., • Proven experience (minimum 3 years) in financial management of competitive funding for research projects., • Strong knowledge of EU and national funding mechanisms, particularly those with complex co-funding structures., • Expertise in project audit management, ensuring compliance with financial regulations. DESIRABLE QUALIFICATIONS • Fluency in English and Spanish (written and spoken)., • Excellent coordination and interpersonal skills, with a service-oriented mindset., • Strong organizational skills, attention to detail, and ability to meet deadlines autonomously., • Proven capacity to navigate multi-stakeholder environments with efficiency and clarity. WHAT WE OFFER • Indefinite contract for scientific and technical activities pursuant to Spanish Law 14/2011, linked to the duration or availability of funds within the PIXEurope Pilot Line, • The opportunity to shape and influence the development of cutting-edge photonic infrastructure with global impact., • A collaborative and interdisciplinary environment at the interface of academia, industry, and innovation., • A competitive salary according to ICFO’s internal scales and a family allowance, if applicable, in line with institutional policy. This position will be dedicated full time to the European Chips JU Pilot Line project PIXEurope directed by Prof. Dr. Valerio Pruneri, within ICFO’s Project Financial Control team. APPLICATION PROCESS Interested candidates should submit a CV and a cover letter outlining their relevant experience and motivation for the position. Applications should be submitted online via: ___ Applications should be submitted online via: The call will remain open until August 27, 2025. Selection will include a pre-screening of applicants based on eligibility and experience, followed by interviews with shortlisted candidates. ICFO is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. For updated information about ICFO, please visit ___ For questions about the application process, please contact: This contract has received funding from the European Union's Horizon Europe under the Grant Agreement # 101213744, Chips Joint Undertaking (Chips JU) and the Spanish Ministry for Digital Transformation and Civil Service, and is supported by funds from the Recovery, Transformation and Resilience Plan (PRTR).

WE ARE HIRING!!!! Neuraxpharm is the leading European specialty pharmaceutical company focused on the treatment of the central nervous system (CNS), including both psychiatric and neurological disorders. It has a unique understanding of the CNS market built over 35 years. Neuraxpharm is constantly innovating, with new products and solutions to address unmet patient needs and is expanding its portfolio through its pipeline, partnerships and acquisitions. The company has more than 1,000 employees and develops and commercializes CNS products through a direct presence in more than 20 countries in Europe, and globally via partners in more than 60 countries. Neuraxpharm is backed by funds advised by Permira. Neuraxpharm manufactures many of its pharmaceutical products at Neuraxpharm Pharmaceuticals (formerly Laboratorios Lesvi) in Spain. Neuraxpharm is searching a vacancy based in Barcelona, Sant Joan Despi: SAP4 Hana FI CO Data Governance Specialist Reporting to the Head of Corporate Controlling, the new position will be responsible for coordinating and leading the SAP4 Hana FI CO data governance at a corporate level for all the entities within the Group. BEING YOUR MAJOR ACCOUNTABILITIES: • Ensure that all data within the company is correctly mapped and integrated as master data in the systems., • Develop, implement, and maintain policies, procedures, and best practices for master data governance and quality., • Analyze systems and data flows from a master data management perspective in accordance with business needs in different countries., • Identify areas for improvement in terms of information structure and flows, automation, traceability of information, and support for the company in best practices and implementation., • Act as a controller to ensure global consistency, data quality, and ease of data use., • Evaluate data integrity techniques and systems to improve data accuracy, • This role will be involved in the month-end closing for both finance and controlling areas WE REQUIRE: • University degree (Economics, Business, IT), • Key user in SAP4 Hana FI, CO-PA is a must with at least 5 years professional work experience in similar role, • Ability to work independently., • Project planning skills, independent, cooperative, results oriented, initiative and critical thinking, consistent and ability for teamwork., • Fluent English. Knowledge of other European languages (Spanish, German, French…) will be valuable., • International experience strongly preferred., • Demonstrated ability to work creatively in a fast-paced and agile environment., • Strong leadership skills, • Ability to work independently and engage wider stakeholders across organization both internally and externally., • Being results-oriented with a proven track record of implementation and project management success., • Showcasing a positive, constructive, team player mentality, • Business acumen and good sense of priorities, structured, results-oriented, and efficient. Superb problem-solving and organization skills., • Convincing, service minded, self-motivated and persuasive personality with ethical values. Positive thinking WE OFFER: • Individual Professional development in a leading European pharmaceutical company with an ambitious international growth strategy., • Economic conditions will be according to the experience and skills provided., • A motivated and committed environment based on a diverse and inclusive culture., • A specialized team focused on our core activity: Improving our patients’ lives.

En Reig Jofre estamos buscando a un/a QA REGULATORY INTELLIGENCE para que pueda contribuir a los diferentes proyectos que estamos desarrollando en la planta productiva ubicada en Sant Joan Despí (Barcelona). Su misión principal será la de proporcionar inteligencia regulatoria accionable al equipo de Cumplimiento Normativo y Calidad, garantizando que las políticas, procedimientos y procesos internos estén alineados con las expectativas regulatorias más recientes, fomentando así una cultura de cumplimiento proactivo. Si te gustan los retos, te sientes cómodo/a en ambientes dinámicos y tienes vocación por la industria farmacéutica ¡no dudes en seguir leyendo! Funciones: • Monitorear de forma continua fuentes regulatorias clave (FDA, EMA, ICH, entre otras autoridades sanitarias y organismos reguladores) para identificar cambios normativos, actualizaciones en guías y tendencias relevantes dentro del sector farmacéutico., • Evaluar el impacto potencial de nuevas disposiciones regulatorias sobre el Sistema de Gestión de Calidad (QMS), garantizando que las auditorías internas contemplen adecuadamente sus implicaciones tanto en la calidad del sistema como del producto., • Elaborar y mantener reportes periódicos de inteligencia regulatoria dirigidos a los equipos de Calidad, Asuntos Regulatorios y otras funciones estratégicas, con el fin de anticipar posibles impactos normativos., • Participar activamente en foros industriales, conferencias especializadas y grupos regulatorios, para mantenerse actualizado sobre tendencias emergente., • Colaborar estrechamente con los equipos de Compliance, QA y Registros para asegurar un cumplimiento normativo proactivo y sostenido., • Administrar bases de datos internas y/o herramientas digitales utilizadas para la gestión de inteligencia regulatoria., • Ser responsable de la gestión y seguimiento de los indicadores clave de desempeño (KPI’s) relacionados con calidad, asegurando su correcta medición, análisis de resultados e identificación de áreas críticas y oportunidades de mejora., • Ejecutar revisiones periódicas del sistema de calidad (Health Quality System Check), para verificar su conformidad, solidez y eficacia operativa., • Diseñar y liderar el plan anual de calidad, alineando las expectativas regulatorias con los objetivos estratégicos internos, tomando como base los resultados del Health Quality System Check., • Coordinar y liderar los Quality Councils a nivel local, asegurando una gobernanza del sistema de calidad conforme a los alineamientos de ICH., • Dar soporte en auditorías internas y externas mediante la provisión de información regulatoria actualizada y relevante., • Impartir formaciones a los equipos internos sobre nuevas regulaciones, desempeño de calidad y sus implicaciones operativas, promoviendo una sólida cultura de calidad en la organización. Aptitudes y experiencia requeridas: • Grado o Licenciatura en Ciencias de la Salud, Experimentales o afines., • Experiencia mínima de 5 años en funciones relacionadas con asuntos regulatorios o calidad dentro de la industria farmacéutica., • Conocimiento profundo de normativas internacionales aplicables (por ejemplo: FDA 21 CFR, ISO 13485, MDR, directrices ICH Q-series, entre otras)., • Capacidad para sintetizar y comunicar información técnica compleja de forma clara, estructura y orientada a la acción., • Nivel avanzando de inglés., • Sólidas habilidades de pensamiento estratégico, análisis crítico y resolución de problemas., • Perfil pragmático, orientado a resultados y con alto nivel de compromiso. Nosotros ofrecemos: • Salario competitivo en función de la capacidad y experiencia del candidato., • Horario flexible de entrada y salida (de 7:30h a 9.30h hasta las 16:30h a 18:30h), • Contrato indefinido., • Plan de compensación flexible (seguro médico, ticket transporte y restaurante, guardería, formación…)., • Formar parte de una empresa líder en el sector farmacéutico. Si cumples con los requisitos y quieres involucrarte en un nuevo reto profesional, no lo dudes ¡Apúntate!

Giesecke+Devrient makes the lives of billions of people around the world more secure. We create trust in the digital age with integrated security technologies in three business areas: Digital Security, Financial Platforms and Currency Technology. We have been a reliable partner for our customers for over 170 years with our innovative solutions for SecurityTech! We are an international technology group and traditional family business with over 14,000 employees in 40 countries. Creating Confidence is our path to success. Trust is the basis of our co-operation within G+D. Maybe soon for you too? We are convinced, that various central banks will introduce a digital version of their currency, a so-called Central Bank Digital Currency (CBDC) like the digital Euro in the coming years. This will create an entirely new market for products and services that fit perfectly with Giesecke+Devrient's product portfolio. It especially requires and outstanding team to deliver a disruptive innovation of that magnitude. For this, we have set-up a team as an independent start-up within G+D advance52 GmbH that has a clear mission for growth and to create a substantial product business. During the next year we are scaling rapidly to meet market demands, and the Software Quality Assurance Architect will be a key part of maintain a high quality. Job Summary The quality, across all levels, of such a CBDC ecosystem is of paramount importance. To help us continue achieving the highest levels of quality, in both the functional and non-functional domains of our CBDC product portfolio, we are looking for a Software Quality Assurance Architect (m/f/d). The challenges in this context are big, but so is our motivation and desire to succeed. In this role, you will be an integral part of the software development team and play an important part in providing the level of trust that G+D has been valued for by its customers for more than 170 years. Your Responsibilities: • Design and maintain the strategies to ensure the highest quality standards across the entire CBDC eco-system, • Define and maintain an adequate risk analysis strategy for all components and the solution as a whole, • Conceptualize and create the frameworks for functional, performance, security and penetration testing, • Architect and build modular and reusable automated testing solutions, • Design, plan, execute, monitor and improve testing process and methodologies, • Research, evaluate, recommend and employ new test tools and frameworks, • Plan and steer testing activities with partners, in the context of non-functional requirements (performance, security), • Engage with customers to understand their requirements and concerns, then derive, design and help implement QA strategies and solutions to address those needs Your Profile: • Expert in constructing test plans and executing against these plans across functional, regression, unit, system, performance, stress and load testing, • Proficient in all steps of the testing pyramid, • Experienced with implementing Continuous Integration and build automation systems, • Skilled in designing WebService/API testing frameworks, • Practised in Source Code Management Tools (git), • Experienced in Mobile testing frameworks and tools (iOS and Android), • Knowledge of security and penetration testing, • DevOps testing knowledge and experience What’s great about working with us? Culture and Diversity: A people-oriented environment with an international team and strong team spirit. Flat hierarchies. Equal Opportunity Employer and LGBT+ friendly. Learning & Growth: Continuous training, mentoring, and career development programs. Flexibility & Balance: Hybrid work model with flexible hours (Mon–Thu 9:30–17:00, Fri 9:00–15:00). Global Impact: You’ll contribute to secure payment solutions used across the world. Perks: Flexible compensation (transport, meals, insurance, nursery), on-site parking, subsidized canteen, and more. Location: Easily accessible by public transport (Bus 88 and 110, Metro L10 ZAL-Riu Vell, PR4 from El Prat) or private vehicle.

Position Summary We are looking for a creative and motivated Graphic Design Intern to join our fast-paced marketing team in Barcelona. The ideal candidate has a passion for visual storytelling, thrives in a collaborative environment, and is eager to contribute to exciting projects that support our global and regional marketing efforts. The Graphic Design Intern will be under the supervision of the Senior Marketing Manager and the Marketing Specialist and will support the Marketing teams in developing compelling visual content across digital, social, and print platforms, ensuring brand consistency and creative excellence. Essential Functions: • Design and produce digital assets for social media, email campaigns, website banners, and newsletters, • Create and layout marketing collateral such as flyers, event signage, presentations, and printed materials, • Support the development and consistency of the brand’s visual identity across digital and physical platforms, • Collaborate with the marketing team to deliver creative content for seasonal product launches and go-to-market campaigns, • Prepare and finalize artwork for both print and digital production, ensuring high quality and accuracy, • Edit and retouch images for product and lifestyle use, maintaining brand standards, • Capture product-focused content using an iPhone for use across digital platforms and marketing materials, • Maintain and organize the digital asset library to ensure efficient access and consistency, • Contribute to the visual execution of brand activations, trade shows, and MX/MTB events, ensuring alignment with global branding and enhancing the on-site experience Skills: • Creativity and strong visual eye, • Communication proficiency, • Positive attitude & energy, • Detail-oriented with good time management, • Team player, • Proficiency in Adobe Creative Suite (Photoshop, Illustrator, InDesign, Premiere), • Basic understanding of motion design (After Effects or similar) is a plus Expected Hours of Work: • Must be available during standard business hours, • Occasional off-hours availability may be required during peak campaign periods or events Required Education and Experience: • Currently pursuing or recently completed a degree in Graphic Design, Visual Communication, or related field, • Strong portfolio showcasing diverse design projects, • High level of English (written and spoken), • Understanding of design principles, layout, and typography, • Familiarity with MX and/or MTB culture is a plus 📩 Sounds like you? Apply now or drop us a message at – we’d love to meet you!

The PreFab Modular Data Center Systems have been driving a tremendous growth to the segment during the last years. The PreFab Data Center Systems Line of Business integrates Schneider products into modular enclosures, test the systems in the factory and deliver the final solution to the country of destination. As Technical Leader LV Expert you will be accountable for the LV design delivered to customers. You will be responsible of developing design proposals, specifications, drawings, and other data to evaluate the feasibility, cost implications, and maintenance requirements of designs or applications. You will identify the project requirements, provide design solutions to meet the customer and site requirements, and ensure the customer’s best interests are protected during the project. Main Responsibilities: During Tender Phase, the Technical Leader LV Expert will be responsible of: • Participates in the programming of the project with the customer or customer representative to understand and document the owner’s project requirements. Influence on solution to drive., • Understand the codes and ordinances local to the opportunity/project., • Solutions Development: Provide appropriate design documents to support the proposal and allow the estimating team to assemble cost for the proposal. These design documents should identify at a minimum the following as applicable:, • Identification of major LV infrastructure equipment, • Bid specifications for the major/long LV lead equipment, • Space and site layout, • Check feasibility with vendors, • Provide estimate to develop the final design documents and construction administration as appropriate for the project., • Solicit, review, and approve sub-consultant proposals to provide a complete set of design documents for the project., • Provide the technical narrative for the critical infrastructure to be incorporated into the proposal., • Performing design improvements primarily to support upgrades and efficient solutions in conjunction with client needs. During Design Phase, the Technical Leader LV Expert will be responsible of: • Utilizing engineering skills and applicable codes and standards to implement systems that are safe, reliable, and economical, • Take the lead for the basis of design for the project, including redundancy requirements, detailed design, connectivity, footprint, validate product selection, etc. of the LV equipment, • Support on System sequence of operation (SOO), • Contributes to team effort by accomplishing related results as needed. During Production and Delivery Phase, the Technical Leader LV Expert will be responsible of: • Manage the support and response to request for information (RFI) of LV equipment, • Assist the production team for clarification, changes, corrections, value engineering, etc. of the design documents for unforeseen site conditions or customer requests, • Provide assistance to the production/project management team for change order requests Main interactions: • Reports to the PreFab Tendering team Leader, • Internal: Technical Leader, SME, Sales Manager, Opportunity Leader, Intra Group suppliers, Project Managers, Quality, Factory, • External: customers and Outside Group suppliers Requirements: • Bachelor’s Degree in an Engineering discipline, Electrical Engineering preferrable, • +Five years experience with Infrastructure Projects within Engineering teams in Multinational companies and global teams., • +3 years technical experience in Data center Solutions including but not limited to Secure Power Systems, Cooling systems, Electrical and Mechanical installations, Logistics, Civil Works., • Previous Customer facing roles preferred, • Electrical panel design experience Prisma, Okken, Blockset background., • 5 years of experience in Power Systems Design., • Experience on simulation tools such as SKM, ETAP or Easypower could be valuable, • Experience with Generators, UPSs, Schneider Electric & APC products background, desired., • Grounding designs as per IEC, IEEE & TIA 607-B standards., • Results oriented, critical thinking and problem-solving skills, • Influence and convince skills, • Decision-making and escalate appropriately when arbitration is required., • Experience in the development of technical documents and drawings, in the preparation of material estimates for bids, in preparing requests for quotations and material purchase requisitions and in the technical evaluation of vendor offers, • Adopting an excellent attitude toward providing system solutions to customer problems., • Proven ability to work independently and provide sound technical advice and constructive support to project managers and customers (directly)., • Ability to generate and foster client relationships while working in a fast paced and competitive business environment., • Capacity to work under pressure in order to meet deadlines., • Excellent organizational skills and attention to detail, • English fluency is a must (C1), • Computer tools at user level: MS Excel, MS Word, MS Project, • Some knowledge on Autodesk REVIT, Autodesk Construction Cloud could be valuable

If you’re looking for a new challenge and have strong experience building scalable data pipelines and integrating SAP systems… keep reading — this opportunity might be for you! We are looking for a Data Engineer (SAP Integration) to join a long-term, stable position within a leading multinational group in the aviation sector. You will be responsible for designing, building, and optimizing robust data pipelines and models to support advanced analytics and financial reporting initiatives across the group. This role is key to ensuring high data quality, reliability, and scalability in a dynamic, cross-functional environment — with a strong focus on SAP financial data and cloud-based platforms. Key Responsabilities: • Design and maintain reliable ETL/ELT pipelines to extract SAP financial data into cloud platforms (mainly AWS: S3, Glue, Redshift)., • Build clean, reusable data models using dbt and automate workflows with Airflow., • Collaborate with stakeholders to understand financial reporting needs and translate them into scalable data solutions., • Ensure data quality, governance, and integrity across all workflows. Requirements: • 2+ years of experience in Data Engineering., • Strong SQL skills and understanding of SAP financial tables (e.g., BKPF, BSEG, COBK)., • Hands-on experience with cloud platforms (ideally AWS) and orchestration tools like Airflow., • Experience integrating SAP into modern data stacks., • Knowledge of SAP BW, SAP Data Intelligence, or basic ABAP for ETL logic. What working with us will offer you: • The chance to take part in challenging projects within a dynamic environment., • A stable position with a clear career development plan., • A permanent contract from day one., • Hybrid remote work format., • Flexible compensation and meal vouchers, among other benefits. If you're interested in this opportunity and would like to know more, feel free to apply so we can get in touch, share all the details, and answer any questions you may have. Agap2 is an equal opportunity employer. We are committed to evaluating all applications based on skills, experience, and achievements. We encourage everyone to apply — all candidates will be treated fairly regardless of race, nationality, gender, age, disability, sexual orientation, gender identity, or any other characteristic.

WE ARE HIRING! CONTROLLING INTERN Neuraxpharm is looking for people who want to make a difference and improve patients’ lives within the CNS area. We want individuals who will go the extra mile and make great things happen. Being part of this team does not mean you are just working for a company, but for a cause! Neuraxpharm is looking for a Controller Intern based in Barcelona (hybrid role) Your mission: Reporting to the HR Controller and supporting both the Corporate and Local HR functions, you will be responsible for optimizing the efficiency of the Human Resources function. You will take part in the digital transformation of HR, as well as in the design and implementation of new processes for the Group’s HR function. Your major accountabilities: • Support in analyses/studies on labour matters., • Ensure accurate employee data entry in the HRIS (SuccessFactors): compensation, personal information, organizational data…, • Participate in audits and data quality checks to ensure accuracy and consistency., • Support Compensation & Benefits projects (participate in defining objectives, scales, goal achievement calculations, merit increase processes, job category reviews, etc)., • Assist in preparing HR reports and dashboards for internal stakeholders., • Support internal audits and reporting related to labour relations metrics and compliance., • Support Coordination of personnel planning., • Support in monthly monitoring and analyse variances in FTE, headcount, and personnel costs versus budget and actuals., • Prepare data for financial audits, non financial audits, ESG reports, surveys, etc, • Collaborate with cross-functional teams to improve HR processes and workflows, aiming to automate and streamline workflows., • Participate in coordination of cross-functional HR projects., • Provide general administrative support to the HR team as needed to support smooth and efficient HR services across the organization. We would like you to have: • Currently pursuing a degree in Human Resources-Labour relations, Business Administration, Psychology, or a related field and/or Master degree with the possibility of an internship relation., • Detail oriented., • Able to manage different projects at the same time, eager to learn and contribute., • Energetic and collaborative., • Eagerness to learn and contribute in a fast-paced environment. HR motivation., • Proficient in Microsoft Office Suite (Excel, Word, PowerPoint)., • Fluent in English and Spanish., • It is mandatory to have the possibility to sign a 6-12 months internship agreement. ABOUT NEURAXPHARM Neuraxpharm is a leading European specialty pharmaceutical company focused on the treatment of the central nervous system (CNS), including both psychiatric and neurological disorders. It has a unique understanding of the CNS market built over 35 years. Neuraxpharm is constantly innovating, with new products and solutions to address unmet patient needs and is expanding its portfolio through its pipeline and acquisitions. The company has c. 1,000 employees and develops and commercializes CNS products through a direct presence in more than 20 countries in Europe, two in Latin America, one in the Middle East and globally via partners in more than 50 countries. Neuraxpharm is backed by funds advised by Permira. Neuraxpharm manufactures many of its pharmaceutical products at Neuraxpharm Pharmaceuticals (formerly Laboratories Lesvi) in Spain. Be part of the team where you can count on us to deliver: • Individual Professional development in a leading European pharmaceutical company with an ambitious international growth strategy., • Attractive remuneration according to the experience and skills provided., • An inspiring leadership team that drives performance., • An inclusive culture promoting diversity across the teams that will inspire you every day with a passionate, a dynamic, a result focused and an expert&excellent team!

iVascular is a fast growing company founded in 2010 in Barcelona (Spain) with the aim of developing medical devices and therapies for the treatment of disorders of the vascular system and to become a reference in the vascular field by enhancing the value of technology and innovation. The team that started iVascular has more than 30 years of experience in the field of vascular devices, being responsible for obtaining one of the first CE marks for a drug-eluting stent more than 20 years ago. We are currently looking for an R&D PROJECT LEADER for our plant located in Sant Vicenç dels Horts (Barcelona). Your main objective will be to lead the development of a delivery system for a medical device, from 2D/3D prototype design to the management of prototype manufacturing, coordination of bench testing, analysis of results and report writing, leading the device verification phase, and preparing the necessary documentation for submission to regulatory authorities. KEY RESPONSIBILITIES: • Prepare the technical planning for assigned projects, applying the methodology implemented in the company., • In collaboration with the department head, prepare project budgets and define the technical and human resources to achieve the technical and economic objectives., • Ensure the feasibility and technical quality of the solutions proposed., • Coordinate and implement the production process for the products developed., • Research and develop improvements in the technical characteristics, quality, and costs of products., • Define purchasing specifications and approve suppliers from the initial stage until the product is transferred to the factory, sending guidelines for subsequent procurement. DESIRED PROFILE: • Industrial Engineering, especially in the mechanical, electromechanical, materials, biomedical fields or a similar one., • High level of English and Spanish., • Minimum 5 years of experience in a similar position., • Previous experience working in an R&D department. Previous experience working with CAD systems (especially Solidworks and Rhinoceros) and Ansys., • High capacity for multidisciplinary work, analytical capacity, integrity, cooperative spirit, communication skills. Innovative sense, high self-esteem, and high expectations for professional development. WHAT WE OFFER: • Permanent contract, stable position within a high-impact strategic project at a company currently expanding internationally and with global reach., • Competitive salary based on experience, plus attractive benefits., • Real growth opportunities in a flexible, collaborative, multidisciplinary, young and dynamic environment., • Flexible compensation (restaurant tickets, transportation, and childcare)., • iWellness service: physiotherapy, gym and cycling club., • Corporate events and gifts., • Company-owned cafeteria., • Work-life balance.

You’ll assist in managing quality incidents, non-conformities, and potential supplier escalations. You’ll be responsible for maintaining supplier documentation, including quality agreements, certifications, ESG evaluations, and legal requirements. At Draxton Barcelona (E&A Headquarters), we are

To help us continue achieving the highest levels of quality, in both the functional and non-functional domains of our CBDC product portfolio, we are looking for a. Software Quality Assurance Architect (m/f/d). Design and maintain the strategies to ensure the highest quality standards across the enti

Create high-quality templates aligned with our communication standards. Monitor and analyze customer contacts handled by agents for quality assurance.

Are you enthusiastic about becoming a highly skilled quality engineer? If so, this position may pique your interest. As a Quality Engineer in the automotive sector, you will be responsible for developing a plan and implementing a systematic approach to ensure that all defined automotive standards, p

Software Quality Assurance Engineer / 6 months / Barcelona (Hybrid) / €300 -€345per day. I am currently looking for a Software Quality Assurance Engineer.

Buscas un nuevo reto donde desarrollar tu carrera y aprender nuevas tecnologías?.Entonces sigue leyendo porque esto te puede interesar.Scalian es una empresa de más de 6.Estamos especializados en dar servicios a diferentes clientes enfocados en Data, Cloud e Inteligencia Artificial.Estás buscando

SAP Information Steward, Talend, Informatica Data Quality, Collibra Data Quality, Trillium, Ataccama, etc. As a Data Quality Analyst, you’ll be part of the team that keeps our clients’ data in top shape. You’ll help monitor, validate, and improve the quality of data across a range of clients u

As a Quality Engineer in the automotive sector, you will be responsible for developing a plan and implementing a systematic approach to ensure that all defined automotive standards, practices, procedures and methods are adhered to by management. Receives and channels complaints regarding customer qu

The QA Engineer is responsible for all aspects of Quality Assurance across multiple software development projects.

Join Rephine Barcelona: Elevate Quality in Life Sciences. If so, we want you on board as an GMP Quality Assurance Technician in Barcelona!.

Senior Verification Engineer – Drive Quality in Next‑Gen RISC‑V CPUs (UVM/SystemVerilog). SystemVerilog and UVM to ensure their next generation of high-performance silicon meets the highest quality standards. Influence design quality from day one; your work directly impacts first-silicon succe