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Who we are: Ventós Group is an international company specialized in the distribution and production of Essential Oils & Aroma Chemicals with the Head Quarters located in Barcelona, Spain. The group has 9 subsidiaries around the world. We believe our people are our most important asset, so we'll offer you a dynamic international working environment with constant opportunities for development. Currently we need to reinforce our team in Ventós Barcelona by adding a Quality Control Technician. Responsibilities: • Perform quality control analysis on essential oils and aroma chemicals, • Carry out chemical tests according to internal specifications and industry standars, • Conduct organoleptic evaluations (taste and smell analysis), • Operate and interpret results using GC-FID and GC-MS instruments, • Participate in the development, validation, and maintenance of analytical methods for gas chromatography, • Collaborate with the Regulatory Affairs teams to ensure product traceability and compliance, • Prepare reports, certificates, and documentation related to quality control, • Support the implementation of continuous improvement processes within the QA department Profile: • Prepare reports, certificates, and documentation related to quality control, • Support the implementation of continuous improvement processes within the QA department, • Degree in Chemistry or related scientific field, • Desirable: Master’s degree or proven expertise in Gas Chromatography and Mass Spectrometry, • Expertise in the Flavour and Fragance industry is a strong asset, • Familiarity with quality standards and analytical protocols in the chemical or cosmetics sector is valued, • Solid knowledge of organic and analytical chemistry, • Experience or interest in natural substances, chemical synthesis, and analytical method development, • High level of English is a must, • Attention to detail, problem-solving mindset, and ability to work independently, • Team spirit, flexibility and proactive attitude We offer a benefits package which includes: • Flexible working hours, • Free language classes and access to other training courses, • Health insurance, • Subsidized meals and breakfast service, • Corporate paddle tennis court for employees and their families Do you think your professional profile fits and this could be a good project for you? Send us your application and tell us why!

Fresh Del Monte is one of the world's leading vertically integrated producers, marketers and distributors of high-quality fresh and fresh-cut fruit and vegetables, as well as a leading producer and distributor of prepared food across the globe. The Group is established in more than 100 countries and has nearly 40.000 employees worldwide. We are looking for a Key Account Manager based in Castelldefels (Barcelona), on a permanent contract. The Key Account Manager maintain the relationship between key distributors and customers as well as internal sourcing and distribution department. The successful candidate will be responsible for the following tasks: • Validate daily customer orders (ECI, Consum), issue weekly invoicing to customers, and reconcile customer debit/credit notes., • Approve suppliers’ weekly invoices, issue the corresponding packaging invoice, validate weekly production yield, and update related accruals., • Monitor packaging stock levels (pots and resealable film) and issue production write offs., • Review weekly P&L and key KPIs (volume, sales, OI, yield/waste and service level)., • Conduct weekly market checks on pricing, new product launches, and competitor activity. -Define the category strategy, including portfolio development, price positioning, and the innovation roadmap. -Develop new customers and business opportunities. -Lead demand planning, volume forecasting, and the resolution of operational or supply issues to ensure business continuity. -Approve packaging purchases with Corporate Procurement (forecasting, costing). -Ensure packaging availability and cost efficiency through proactive supplier management and forecasting. -Manage POS activities and coordinate with Marketing, Quality, Logistics, Finance, and Procurement. Skills required: • Bachelor’s degree from business school., • Fundamental experience as sales (min. 3/5 years’ experience) with B2B preferably in FMCG company., • Fluent in English., • Managing external relationships with third parties, coordination projects., • Financial acumen. Acknowledgement of financial systems and reporting; planning and forecasting., • Analytical skills: good numeracy, understanding P&Ls, financial reports., • Entrepreneurial., • Strategic thinking: experienced in developing, preparing, and presenting strategic plans and ability to challenge the plans presented by distributor., • Excellent communicational/organizational skills., • IT-experience: ability to create and prepare Power Point presentations, good Excel skills., • Presentation: senior level presentation & communication skills required. Ability to communicate at all levels., • Able to travel across the Region.

Join our team as Plant Engineer in Fawley, UK (initial 12-month assignment in Barcelona, Spain) Discover Tradebe Tradebe is a group of industrial businesses committed to creating a more sustainable planet and making a significant contribution to human wellbeing. In the UK, we are leaders in recycling, energy recovery, and circular economy solutions, managing environmental liabilities in a sustainable way. Tradebe’s Fawley facility is a key site for hazardous waste incineration, ensuring safe, compliant, and efficient treatment of complex waste streams while contributing to environmental protection and resource recovery. What will you do? Make an impact! Join Tradebe as a Plant Engineer and play a key role in optimising industrial hazardous waste incineration processes. You will ensure safe, efficient, and compliant operations while driving continuous improvement initiatives. Starting with a 12-month assignment in Barcelona, you will gain deep technical knowledge before transitioning to our Fawley site, acting as a key link between Global and UK operations. Key Responsibilities • Gain in-depth knowledge of hazardous waste treatment technologies (biological, chemical, and physical) during your initial assignment in Barcelona, • Collaborate with operations and process teams to understand control systems, monitoring methods, and optimisation techniques, • Transfer knowledge and best practices from Global sites to the UK facility, • Optimise plant processes to ensure safety, compliance, and operational efficiency, • Lead troubleshooting and root cause analysis to resolve technical issues, • Support engineering projects, including commissioning, testing, and implementation of new equipment, • Contribute to investment projects, working closely with the Engineering Manager in Fawley, • Monitor KPIs and drive continuous improvement across performance, cost, and environmental impact Do you have what it takes? • Master’s degree in Chemical or General Engineering, • 5+ years of experience in chemical, environmental, or process engineering industries, • Strong understanding of plant operations, process optimisation, and control systems (incineration knowledge is a plus), • Excellent analytical, problem-solving, and communication skills in multicultural environments, • Project Management according to the British interpretation (PRINCE2 or similar frameworks) We expect from you to Be accountable, Drive results, Embrace change, and collaborate effectively! What’s in it for you? • Competitive salary package (base + bonus, negotiable), • International career exposure with a 12-month assignment in Barcelona, • Relocation support and mobility opportunities within a global organisation, • Pension scheme and flexible benefits, • Opportunity to work on impactful sustainability and industrial projects Ready to make a difference? Apply now! #EquipoTradebe #Sustainability #TradebeJobs If this opportunity doesn’t match your expectations but you are interested in developing your career in a company committed to circular economy and sustainability, register on our Career Page and stay connected for future opportunities 🚀 Tradebe is committed to ensuring selection processes based on merit and skills, free from bias related to age, gender, sexual orientation, religion, or nationality. We believe in equal opportunities — and we actively work to promote them.

🤗 ¿Quiénes somos? 🤗 Edenred, empresa reconocida como una de las “100 mejores empresas para trabajar en España” en 2024 y certificada como Great Place to Work, nació llena de ilusión hace más de 60 años, siendo pioneros en el desarrollo de beneficios sociales para equipos y operando en la actualidad en 45 países, ofreciendo soluciones como plataforma digital a 60 millones de usuarios. Desde nuestros inicios, hemos mantenido vivo un sueño que sigue presente en todas las decisiones de la compañía: generar conexiones de valor que fomenten el crecimiento de nuestros stakeholders y de la sociedad en general. 😊 Misión del puesto 😊 Como Legal & Compliance Specialist serás responsable de impulsar y dar soporte al día a día del departamento Legal, con especial foco en la gestión y revisión de contratos, garantizando que todas las operaciones se desarrollen conforme a la normativa vigente. Además, participarás activamente en las iniciativas de Compliance, colaborando en la implantación, seguimiento y mejora de políticas internas, controles y procedimientos que aseguren el cumplimiento regulatorio dentro de la organización. 📚Tus principales responsabilidades📚 • Elaboración, revisión y negociación de contratos con clientes, partners y proveedores., • Revisión de licitaciones públicas y apoyo en documentación para concursos., • Soporte jurídico en proyectos transversales, así como en materia societaria, litigación y consultas legales internas., • Desarrollo e implementación de políticas y procedimientos vinculados a contratación y gestión de riesgos legales., • Apoyo en iniciativas de Compliance, contribuyendo al mantenimiento del sistema de cumplimiento interno., • Participación en la creación, actualización y difusión de políticas internas, código ético y controles de cumplimiento., • Monitorización del cumplimiento normativo y apoyo en la identificación y mitigación de riesgos de cumplimiento., • Colaboración en formaciones internas y en la gestión de consultas o incidencias relacionadas con Compliance. 🤓 Requisitos deseables 🤓 • 2-3 años de experiencia con dedicación en contratación y/o compliance bien en despacho de abogados o en departamento jurídico de empresa., • Conocimiento jurídico sólido en contratación comercial, anticorrupción, PBC‑FT, prevención del fraude y cumplimiento normativo., • Habilidad para redactar, revisar y negociar contratos, así como para elaborar políticas, procedimientos y comunicaciones internas., • Capacidad analítica para identificar riesgos legales, realizar análisis jurídicos y seguir cambios normativos., • Comunicación clara, transmitiendo conceptos legales de forma comprensible a perfiles no jurídicos., • Trabajo colaborativo y autonomía, con orientación al detalle y capacidad para gestionar múltiples tareas y plazos., • Interés por Compliance y legal‑tech, aprendizaje rápido y habilidad para apoyar en formaciones jurídicas internas., • Idiomas: Español. Inglés avanzado. 🤗 ¿Qué Podemos ofrecerte? 🤗 Edenred está aquí para ofrecerte un montón de beneficios que te ayudarán a sentirte bien y a equilibrar tu vida laboral y personal. ¡Échales un vistazo ya que están pensados especialmente para ti y tu bienestar! • Ticket Restaurant 11€/día de lunes a jueves entre septiembre y junio., • Flexibilidad horaria en entrada y salida, además de jornada intensiva todos los viernes del año así como los meses de julio y agosto., • Formato hibrido de trabajo: hasta 8 días de teletrabajo al mes., • Office Day: día semanal en la oficina con desayuno, café y fruta incluida., • Entorno dinámico y multidisciplinar., • Actividades en días clave como voluntariados, Women & Pride week, cena de navidad, entre otras., • Y no menos importante, ¡un ambiente laboral de 10! ¿A qué esperas para que te podamos conocer? Edenred se basa en la meritocracia. Vienes tal y como eres y contribuyes. De hecho, el Grupo Edenred reconoce, contrata y desarrolla todos los talentos y singularidades. Nos comprometemos a prevenir cualquier forma de discriminación y a ofrecer igualdad de oportunidades a todos nuestros candidatos, independientemente de su género y expresión de género, discapacidad, origen, creencias religiosas y orientación sexual o cualquier otro criterio.

At Rob Surgical we are looking to hire a Process Engineering Quality Assurance Technician to join our Quality team and support the continuous improvement and validation of our manufacturing and quality processes. 🧬 About us We are a healthtech company specialized in the development of advanced robotic systems for high-precision minimally invasive surgery. Founded in 2012 as a spin-off from UPC and IBEC, our mission is clear: to make robot-assisted surgery more accessible, precise, and efficient worldwide. 🔍 What will your mission be? As a Process Engineering QA Technician, you will play a key role in ensuring the effectiveness of our Quality Management System (QMS) by supporting the validation master plan, calibration program, and process quality activities. You will work closely with product managers, project managers, developers, and manufacturing teams to ensure quality and regulatory compliance across the entire product lifecycle. 🛠 Your main responsibilities will include: Quality Management System • Drafting and reviewing documentation related to QMS processes., • Participating in the maintenance of risk analyses for QMS processes., • Monitoring and maintaining quality KPIs., • Conducting regular inspections in the production plant to verify process control and compliance with procedures., • Organizing and participating in quality meetings., • Supporting the transfer from design to production, including control plans and control methods., • Training manufacturing personnel when required., • Supporting the design and construction of test rigs for design and manufacturing validation., • Writing validation protocols and reports., • Participating in validation execution and monitoring progress of the validation plan., • Preparing validation maintenance reports and monitoring equipment, facilities, and services., • Participating in validations related to:, • Clean rooms, • Ethylene oxide and wet steam sterilization systems, • Computerized systems, • Analytical test methods, • Maintaining and updating facility and process risk analyses., • Monitoring the calibration program and reporting progress., • Developing and updating calibration procedures., • Participating in calibration activities and issuing calibration reports., • Supporting internal and external audits., • Collaborating in the preparation of annual R&D reports and department budgets., • Supporting administrative tasks related to documentation, digitalization, and archiving., • Contributing to maintaining an organized and efficient work environment. 🎓 What are we looking for? • Bachelor’s degree in Industrial Engineering is highly valued., • Experience level: 3+ years of experience, • Experience in medical devices and/or pharmaceutical industry is highly valued., • Professional working proficiency in English., • Advanced Microsoft Office user., • Experience working with ERP environments. 📚 Valuable knowledge Experience or training related to: • ISO 17025 – Calibration laboratories, • ISO 14644 – Clean rooms, • ISO 11135 / ISO 14937 – Sterilization of medical devices, • ISO 14971 – Risk management for medical devices, • GAMP5 – Validation of computerized systems, • GMP and validation regulations, • Metrology or microbiology 💡 We are looking for someone who is… • Detail-oriented but able to understand the big picture., • Analytical, proactive, and collaborative., • Meticulous, organized, and efficient., • A strong communicator with teamwork. 🎯 What do we offer? • Full-time permanent contract., • Salary aligned with profile and experience., • Flexible working hours., • Monthly fruit and vegetable box 🍎, • Opportunity to work on cutting-edge surgical robotics technology., • Professional development in a highly innovative and regulated environment., • A dynamic and collaborative team where your work has real impact on patients’ lives.

Do you dream of working in a company that is driven by a meaningful purpose? An inclusive company that empowers you to do your best and be innovative? Discover the opportunity to join an international, dynamic, and responsible company that fosters the development of all its people around the world. Every day, we empower employees to achieve more and experience exciting careers. Find out how our values and unique position make Schneider Electric a top 25 employer of choice, according to LinkedIn. Join Schneider Electric and power your career! As a global specialist in Energy Management with operations in more than 100 countries, Schneider Electric offers integrated solutions across multiple market segments, including leadership positions in Utilities & Infrastructures, Industries & Machine Manufacturers, Non-residential Buildings, Data Centers & Networks and Residential. Focused on making energy safe, reliable, efficient, productive and green, the company’s 130,000 plus employees achieved sales of about 25 billion EUR in 2020, through an active commitment to help individuals and organizations make the most of their energy. The Mid Level Electrical Project Engineer is responsible for understanding the technical requirements of the project. He or she shall thoroughly understand the design documents, specifications, references, and project scope. The Senior Project Engineer’s role includes coordinating and preparing all technical documentation to build a prefab solution according to customer requirements within time schedule and the defined quality. Strict attention to detail, understanding of time constraints, and implications of proper documentation all add up to an effective Senior Project Engineer. As part of the engineering team the Project Engineer will be working closely with Project Managers, Technical Leaders, Junior Project Engineers and Production Specialist (Factories), this position is responsible for the technical portion of projects at execution stages. What will you do? • Thoroughly understand the design documents, specifications, references, and project scope., • Keep minutes for all regular and technical design meetings., • Identify, review, collect, verify and store all project technical documents as they are available during the project., • Maintain the general project files according internal procedures (Autodesk Construction Cloud, Sharepoint etc…), • Maintain the Engineering issues Log & Project Engineer Book. (Sharepoint folder), • Develop Approval drawings to meet customer scope (Submittal Package), • Perform change management for design documents and customer submittals, • Track all technical design deviations and notify project/ design team for resolution., • Manage all engineering works schedule and assign tasks to designers and SME’s. (specialists), • Develop major BOM (Bill of Material) for the project., • Coordinate internal periodic design reviews with designers and SME’s (Execution phase), • Create and distribute submittal requests based on project requirements., • Maintain and track submittals and shop drawings, • Maintain and track engineering hours budget., • Maintain current design documents with all addenda and redlines., • Perform QC during the integration phase to ensure compliance with design documents., • Manage handover of all engineering documentation to Factory Production Specialists, • Prepare all final documentation for the project including (as built drawings, certificates, O&M documents, Spare Part lists), • Secure all warranties and guarantees from subcontractors and vendors as defined in the design documents, specifications, and contract., • Ensure all changes to the design documents are redlined to manage the final as-built documents. General duties include: • Coaching Junior Project Engineers during large or complex projects while working together in a customer project, • Working with Technical Leaders or Project Managers to deliver technical information to customer on time., • Working with Factory Production Specialist to resolve questions during the execution of the project, • Establishing, maintaining, conducting, and policing detailed procedures for the submittal review, coordination, approval, and distribution of shop drawings, samples, etc., • Establishing and maintaining all Project Engineering files related to subcontract and bid package records, plans, specifications, changes, clarifications, and as-built documents. About you What qualifications will make you successful? • Education University Bachelor’s degree in Engineering Programs (Electrical or Mechanical Engineering are preferred) Experience (not mandatory but very valuable): Data Center critical infrastructure knowledge (Power, Cooling, Monitoring) Building construction or industrial installations (Cabling, lighting, piping, plumbing) • Skills The following skills apply to this position: Coordinate for project documentation from electrical, mechanical, plumbing, architectural, and structural discipline to meet customer requirements and production constraints. Working with other team members, Technical Leaders, contractors/vendors and consultants to resolve technical issues and to ensure the quality and integrity of engineering design executions. Optimizing designs in compliance with relevant regulatory codes, standards and best practices. Proven skills in written and oral communication of technical information. Excellent communication, organization and teamwork skills with the ability to pay a high level of attention to detail. Capacity to work under pressure in order to meet deadlines. Functional knowledge using Microsoft Office suite, Autodesk REVIT, Autodesk Construction Cloud , AutoCAD 2D and Adobe Acrobat Pro. Experience working in REVIT (preferred) Fluent in English If you would like to have: • Exciting job in an international company, with opportunities to lead and contribute to different projects & actions (e.g. CSR, charity, Employer Branding, Well-Being), • Work in a diverse and supportive team of professionals, • Buddy, mentor & induction training - that will help you to smoothly find yourself in our company, • Special training tailored to your needs and career goals, • No formal dress code - we welcome people as they are and perceive diversity as value for the company, • Possibility to use foreign languages and to collaborate with cross-region teams ....share your CV (in English) with us. At Schneider Electric, we believe access to energy and digital is a basic human right. We empower all to do more with less, ensuring Life Is On everywhere, for everyone, at every moment. We provide energy and automation digital solutions for efficiency and sustainability.

Buscamos un/a Sales Assistant para incorporarse al equipo de OPKO Health Europe en nuestras oficinas de Hospitalet de Llobregat. 🔹 Funciones: -Dar soporte administrativo a la red de ventas de la línea Humana. • Delegados de Venta, • Gerencia, • Contratos, • Aprobaciones -Gestionar los pedidos que llegan a través de los sistemas y correos electrónicos. -Canalizar y atender llamadas telefónicas de clientes. -Dar apoyo a la persona responsable de ventas. -Archivar documentalmente todas las operaciones para su posterior revisión o auditorias. 🔹 Requisitos : -Experiencia mínima de 1 año en puesto de similares características. -Formación Profesional Administrativa o similar. -Imprescindible experiencia en SAP y conocimientos de Excel. -Muy valorable experiencia en CRM. Que ofrecemos: 📍 Ubicación: Hospitalet de Llobregat 📄Contrato inicial temporal con posibilidad de incorporación indefinida. 🕒 Jornada completa ⏰ Horario flexible 💼Salario competitivo acorde al sector y a la experiencia aportada. Si quieres formar parte de una compañía en crecimiento, ¡te estamos buscando!

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. POSITION OVERVIEW ICFO is seeking a Procurement Technician to support the operational deployment of the PIXEurope pilot line. The selected candidate will be responsible for managing the procurement needs of the project – including public tenders, orders, deliveries, and associated documentation – and providing basic legal counsel support to ensure that contracts and agreements are properly executed. The Procurement Technician will work closely with the Pilot Line Procurement and Financial Manager, the technical staff to establish requirements and provide procurement and legal guidance, and the Director of the Strategic Initiative. The role will also involve close collaboration with ICFO’s Legal Team, Projects Financial Control Team, and Finance Team. The position will operate under the supervision of the Legal Team – particularly the procurement staff – who will ensure that all activities are carried out in full alignment with ICFO’s internal procedures and compliance requirements. KEY RESPONSIBILITIES • Manage all phases of procurement procedures for the PIXEurope pilot line, from planning and tender preparation to delivery and invoicing., • Work with technical staff to define requirements, advise on procurement options, and ensure timely acquisition of goods and services., • Prepare and publish tender documents in compliance with public procurement regulations and ICFO’s internal policies., • Coordinate the evaluation of offers and preparation of contractual and administrative documentation., • Liaise with suppliers, project partners, and internal stakeholders to ensure timely and accurate execution of procurement processes., • Maintain accurate and organized procurement and contractual records in both physical and electronic formats., • Provide the Pilot Line with basic legal counsel support, including reviewing and preparing project-related contracts, agreements, and memorandums of understanding., • Support in audits and financial justification for public/European funding. QUALIFICATIONS AND EXPERIENCE REQUIRED The ideal candidate will bring: • A university degree in Law, Business Administration, Political Science, or a related discipline., • At least 2 years of experience in public procurement or contract management, ideally in the public sector or a research environment., • Knowledge of the Spanish Public Sector Contracts Law and procurement procedures., • Fluency in English, Spanish, and Catalan (written and spoken)., • Strong organizational, communication, and problem-solving skills., • Proficiency with office and collaborative tools (e.g., MS Office, Teams, SharePoint). Additional skills and experience that will be valued: • Knowledge of legal counsel functions in a project-based environment., • Experience in procurement of scientific or technical equipment., • Familiarity with EU-funded projects (e.g., Horizon Europe, Chips JU) – valued but not required., • Experience in process optimization and continuous improvement of procurement tools and workflows. WHAT WE OFFER • Indefinite contract for scientific and technical activities pursuant to Spanish Law 14/2011, linked to the duration of the Pilot Line initiative., • A unique opportunity to shape and drive a high-impact European initiative at the forefront of photonic innovation., • Integration into a vibrant, international, and multidisciplinary environment at ICFO., • Integration into ICFO’s vibrant, multidisciplinary, and international research community., • A strategic position in a project that will define the future of European photonics., • A competitive salary according to ICFO’s internal scales and a family allowance, if applicable, in line with institutional policy. APPLICATION PROCESS To apply, please submit your resume, a cover letter outlining your experience and contact information for two professional references. Applications should be submitted via LinkedIn or the ICFOjobs platform Selection will include a pre-screening of applicants based on eligibility and experience, followed by an interview with a short-list of candidates. Candidates will be notified of the outcome within 15 days of the interview. 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 PIXEurope is co-funded by the Chips Joint Undertaking and national funding authorities of the Participating States, Spain, Ireland, The Netherlands, Finland, Belgium, Portugal, Poland, Austria , France, Italy, United Kingdom. In particular, it is co-funded by Spain through the Ministry for Digital Transformation and Civil Service under reference CJU-010000-2025-0005, as part of the Recovery, Transformation and Resilience Plan (PRTR).

We are currently looking for a talented and highly motivated Technical Lead to join an innovative team focused on delivering high-quality, data-intensive solutions and driving technical excellence across the engineering community. In this role, you will play a key part in defining, designing, and implementing advanced AI-based and data-driven technical solutions within a complex, large-scale environment. You will help bring clarity to story-level delivery, remove blockers, and ensure fast, high-quality feature development aligned with strategic business goals. You will also contribute to product architecture, design robust and scalable solutions, and ensure engineering standards remain high across development practices. In addition, you will promote innovation, continuous improvement, and a collaborative, product-oriented culture. Key Responsibilities: 1. Technical Leadership • Define and document architecture blueprints aligned with product strategy and roadmap., • Determine the best technical approaches to build, secure, operate, and maintain products. 2. Product & Feature Delivery • Ensure product backlogs are refined and that features and user stories meet the agreed definitions of done., • Clarify engineering questions and help ensure robust story definitions. 3. Engineering Excellence • Define and enforce high standards for code quality, testing, assurance, and security., • Maintain a strong automated testing strategy, aligned with a zero-manual-testing mindset., • Improve and enhance automated deployment and validation processes. 4. Cloud & Infrastructure • Lead technical solutions across multi-cloud environments, especially Azure and AWS., • Promote and implement DevSecAIOps practices and automation improvements. 5. Collaboration & Communication • Foster strong collaboration between engineering teams, product leadership, and business stakeholders., • Communicate complex technical decisions clearly to non-technical audiences. 6. Risk & Compliance • Identify and manage technical risks, technical debt, and compliance requirements., • Ensure auditable evidence of requirement fulfilment, adherence to security standards, and operational readiness. 7. Mentorship & Team Development • Mentor team members, encourage knowledge sharing, and help develop technical capabilities across the team., • Promote psychological safety and high engagement within the engineering environment. Requirements: • Minimum 5 years of experience in technical leadership roles within data-intensive and AI-driven environments., • Strong hands-on experience delivering production-ready applications with frontend (Next.js), backend (Python), and data / ML components., • Proven experience designing CI/CD pipelines and workflows using tools such as GitHub Actions, Trunk-Based Development, and E2E test integration., • Solid understanding of DevSecAIOps practices and secure coding standards., • Experience working in agile environments, using tools such as Jira for backlog refinement and story estimation., • Experience working with teams using AI tools across the SDLC (e.g. GitHub Copilot, Cursor, Claude Code)., • Strong collaboration and communication skills, with the ability to mentor and guide engineering teams., • Fluent English. Nice to Have: • Familiarity with Docker and Kubernetes., • Experience with observability and monitoring tools, preferably Datadog., • Background in automation frameworks and testing strategies aligned with zero-manual-testing., • Knowledge of Confluence or similar tools for technical documentation., • Experience leading cross-functional teams in distributed environments., • Understanding of enterprise security frameworks and auditability requirements. About You: • Passionate about using software engineering and technology to create business impact., • Strong communicator, able to explain complex topics clearly., • Pragmatic, disciplined, and data-driven in decision-making., • Curious, creative, and committed to continuous learning., • Comfortable working in dynamic, fast-paced environments with structured and hypothesis-driven thinking., • Available to work on-site in Barcelona 2–3 days per week. This is a high-impact role for someone who enjoys working close to engineering, shaping internal platforms and enabling teams to deliver software efficiently, securely and at scale within a global airline and technology environment. If this resonates with your profile, feel free to reach out. Agap2 es una empresa que ofrece igualdad de oportunidades, por ello nos comprometemos a tratar todas las candidaturas por igual en función de sus capacidades, logros y experiencia. Animamos a cualquier persona a presentar su candidatura que será tratada con igualdad de oportunidades independientemente de su raza, nacionalidad, sexo, edad, discapacidad, orientación sexual, identidad de género o cualquier otra característica.

Who we are: Ventós Group is an international company specialized in the distribution and production of Essential Oils & Aroma Chemicals with the Head Quarters located in Barcelona, Spain. The group has 9 subsidiaries around the world. We believe our people are our most important asset, so we'll offer you a dynamic international working environment with constant opportunities for development. Currently we need to reinforce our team in Ventós Barcelona by adding a Quality Control Technician. Responsibilities: Perform quality control analysis on essential oils and aroma chemicals Carry out chemical tests according to internal specifications and industry standars Conduct organoleptic evaluations (taste and smell analysis) Operate and interpret results using GC-FID and GC-MS instruments Participate in the development, validation, and maintenance of analytical methods for gas chromatography Collaborate with the Regulatory Affairs teams to ensure product traceability and compliance Prepare reports, certificates, and documentation related to quality control Support the implementation of continuous improvement processes within the QA department Profile: Prepare reports, certificates, and documentation related to quality control Support the implementation of continuous improvement processes within the QA department Degree in Chemistry or related scientific field Desirable: Master’s degree or proven expertise in Gas Chromatography and Mass Spectrometry Expertise in the Flavour and Fragance industry is a strong asset Familiarity with quality standards and analytical protocols in the chemical or cosmetics sector is valued Solid knowledge of organic and analytical chemistry Experience or interest in natural substances, chemical synthesis, and analytical method development High level of English is a must Attention to detail, problem-solving mindset, and ability to work independently Team spirit, flexibility and proactive attitude We offer a benefits package which includes: Flexible working hours Free language classes and access to other training courses Health insurance Subsidized meals and breakfast service Corporate paddle tennis court for employees and their families Do you think your professional profile fits and this could be a good project for you? Send us your application and tell us why!

Definir y liderar la estrategia global de compras indirectas, asegurando la optimización de costes, la eficiencia operativa y la calidad del servicio, alineando las necesidades del negocio con un modelo de procurement escalable en un entorno industrial intensivo en mano de obra y con operaciones internacionales. Responsabilidades principales Definir e implementar la estrategia global de compras indirectas Liderar la gestión de categorías, tales como: Civil works. Servicios generales (facility management, limpieza, seguridad) Recursos humanos (ETT, formación, servicios laborales) IT y telecomunicaciones MRO y servicios industriales Energía y utilities Viajes, flota y gastos corporativos Impulsar iniciativas de optimización de costes y eficiencia Definir e implementar políticas, procesos y governance de compras Liderar procesos de sourcing estratégico y negociación con proveedores clave Desarrollar y gestionar relaciones con proveedores estratégicos (SRM) Asegurar cumplimiento normativo, contractual y de auditoría Colaborar estrechamente con: Operaciones / plantas Finanzas Recursos Humanos IT Liderar proyectos de transformación digital en procurement (P2P, e-sourcing, automatización) Definir y hacer seguimiento de KPIs (ahorros, compliance, performance proveedores) Gestionar y desarrollar el equipo de compras indirectas a nivel regional/global Perfil requerido Ingeniería +10–15 años de experiencia en compras, con al menos: Experiencia relevante en compras indirectas Experiencia liderando equipos Experiencia en entorno: Industrial / manufacturero Internacional / multi-site Sólida experiencia en gestión de múltiples categorías indirectas Experiencia en negociación compleja y gestión de proveedores estratégicos Conocimiento de herramientas y procesos: Procure-to-Pay (P2P) Strategic sourcing Plataformas digitales (SAP, Ariba, Coupa u otras) Nivel biligue de inglés (imprescindible)

MEDICAL AFFAIRS Ophthalmology En Salvat buscamos incorporar un perfil de Medical Affairs Ophthalmology, dispuesto a marcar la diferencia. ¿Quiénes somos? Somos Grupo Farmacéutico Salvat , fundada en Barcelona en 1955 y llevamos 70 años contribuyendo a crear una vida más saludable y feliz con productos emblemáticos como Cristalmina, Cetraxal, Monolitum y Salvacolina . Presencia internacional. Operamos en + de 60 países, con plantas de producción en Barcelona, Madrid y Miami. Innovación y capacidades . Contamos con I+D propia , innovamos y desarrollamos soluciones en las áreas terapéuticas de oftalmología, otorrinolaringología y gastroenterología , además de abordar el ámbito de la salud en Consumer Health y ofrecer servicios CDMO , donde ambicionamos ser un player relevante. Excelencia certificada . Estamos orgullosamente certificados por la FDA y reconocidos con calificación excelente en el Plan Profarma del Ministerio de Industria. Esto respalda nuestro compromiso con la excelencia y ética empresarial . Proyecto New Salvat . Estamos inmersos en un ambicioso proyecto transformador que busca crear un Salvat más fuerte, más ágil y competitivo. Si te gustan los retos y quieres disfrutar dejando una huella positiva , Salvat es tu lugar. Nuestra cultura . Vivimos nuestros valores AACT (Ambición, Accoountability, Colaboración y Transparencia) en el día a día, creemos en el potencial de las personas y fomentamos entornos de donde cada persona pueda crecer y dar su mejor versión. ¿Qué buscamos? El Medical Affairs Ophthalmology será responsable de proporcionar soporte médico-científico en el desarrollo y ejecución de planes médicos en el área de oftalmología. Reportando al Head of Medical Affairs, este rol representa el enlace clave entre las áreas médico-científica y comercial, asegurando la integración de la evidencia clínica y las actividades operativas y estratégicas de la compañía. Tus principales responsabilidades serán: Soporte Médico-Científico: Apoyo médico a los equipos internos, incluidas las áreas de marketing, ventas, (tanto en la elaboración de materiales como en establecer estrategias conjuntas para las diferentes áreas terapéuticas y los diferentes productos), regulatorio (en la elaboración de documentación necesaria) e I+D (en la valoración de posibles proyectos a desarrollar. Preparar materiales médicos basados en evidencia científica Relaciones con KOLs: Establecer y mantener relaciones sólidas con líderes de opinión clave y otros profesionales de la salud Facilitar reuniones científicas y grupos de discusión para recopilar información del mercado Generar proyectos de valor con Sociedades Científicas en el área terapéutica de oftalmología. Estudios clínicos: Apoyar la implementación de ensayos clínicos, estudios observacionales y generación de datos en práctica clínica (RWE) Colaborar en la revisión y aprobación de protocolos de investigación y publicaciones científicas Compliance: Garantizar el cumplimiento de la normativa de buenas prácticas en todas en todas las actividades médicas realizadas Participar en la formación y capacitación del equipo sobre normativas y buenas prácticas clínicas Estrategia médica: Contribuir al desarrollo de planes médicos estratégicos alineados con los objetivos de la compañía Revisión y análisis de publicaciones científicas / guías de manejo clínico y monitorizar las tendencias en el campo médico relevante Patient Advocacy: Colaboración estrecha con asociaciones de pacientes para promover un entendimiento profundo de sus necesidades Perfil ideal Formación universitaria en ciencias de la salud (preferiblemente Medicina, Farmacia o Biomedicina) Experiencia mínima de 5 años en departamento médico, imprescindible experiencia en el área de oftalmología Capacidad de para mediar y construir relaciones con los diferentes stakeholders (internos y externos) Habilidades de comunicación efectiva Dominio del inglés para la implicación en proyectos internacionales Habilidades: Con habilidades técnicas y conocimientos en el área de Medical Affairs (o similar) , buscamos: Con experiencia en Oftalmología con capacidad de Autocrítica , Ganas de Superación y de Aprendizaje constantemente, Proactividad , Capacidad de esfuerzo y de trabajo , Capacidad de búsqueda de soluciones alternativas a las adversidades. Motivación ¿Qué te ofrecemos? Formar parte de una empresa sólida e innovadora, en un momento de transformación y crecimiento. Un entorno colaborativo donde se valora tu iniciativa y tus ideas. Oportunidades de desarrollo profesional real, participando en procesos clave del área y trabajando bajo estándares GMP. Paquete de beneficios y aprendizaje continuo en un entorno regulado. Horario Flexible y jornada intensiva los viernes y en verano. ¿Quieres formar parte de este proyecto transformador? Aplica para más información ¡Vamos a construir juntos el futuro de Salvat!

We are currently looking for a talented and highly motivated Technical Lead to join an innovative team focused on delivering high-quality, data-intensive solutions and driving technical excellence across the engineering community. In this role, you will play a key part in defining, designing, and implementing advanced AI-based and data-driven technical solutions within a complex, large-scale environment. You will help bring clarity to story-level delivery, remove blockers, and ensure fast, high-quality feature development aligned with strategic business goals. You will also contribute to product architecture, design robust and scalable solutions, and ensure engineering standards remain high across development practices. In addition, you will promote innovation, continuous improvement, and a collaborative, product-oriented culture. Key Responsibilities: 1. Technical Leadership • Define and document architecture blueprints aligned with product strategy and roadmap., • Determine the best technical approaches to build, secure, operate, and maintain products. 2. Product & Feature Delivery • Ensure product backlogs are refined and that features and user stories meet the agreed definitions of done., • Clarify engineering questions and help ensure robust story definitions. 3. Engineering Excellence • Define and enforce high standards for code quality, testing, assurance, and security., • Maintain a strong automated testing strategy, aligned with a zero-manual-testing mindset., • Improve and enhance automated deployment and validation processes. 4. Cloud & Infrastructure • Lead technical solutions across multi-cloud environments, especially Azure and AWS., • Promote and implement DevSecAIOps practices and automation improvements. 5. Collaboration & Communication • Foster strong collaboration between engineering teams, product leadership, and business stakeholders., • Communicate complex technical decisions clearly to non-technical audiences. 6. Risk & Compliance • Identify and manage technical risks, technical debt, and compliance requirements., • Ensure auditable evidence of requirement fulfilment, adherence to security standards, and operational readiness. 7. Mentorship & Team Development • Mentor team members, encourage knowledge sharing, and help develop technical capabilities across the team., • Promote psychological safety and high engagement within the engineering environment. Requirements: • Minimum 5 years of experience in technical leadership roles within data-intensive and AI-driven environments., • Strong hands-on experience delivering production-ready applications with frontend (Next.js), backend (Python), and data / ML components., • Proven experience designing CI/CD pipelines and workflows using tools such as GitHub Actions, Trunk-Based Development, and E2E test integration., • Solid understanding of DevSecAIOps practices and secure coding standards., • Experience working in agile environments, using tools such as Jira for backlog refinement and story estimation., • Experience working with teams using AI tools across the SDLC (e.g. GitHub Copilot, Cursor, Claude Code)., • Strong collaboration and communication skills, with the ability to mentor and guide engineering teams., • Fluent English. Nice to Have: • Familiarity with Docker and Kubernetes., • Experience with observability and monitoring tools, preferably Datadog., • Background in automation frameworks and testing strategies aligned with zero-manual-testing., • Knowledge of Confluence or similar tools for technical documentation., • Experience leading cross-functional teams in distributed environments., • Understanding of enterprise security frameworks and auditability requirements. About You: • Passionate about using software engineering and technology to create business impact., • Strong communicator, able to explain complex topics clearly., • Pragmatic, disciplined, and data-driven in decision-making., • Curious, creative, and committed to continuous learning., • Comfortable working in dynamic, fast-paced environments with structured and hypothesis-driven thinking., • Available to work on-site in Barcelona 2–3 days per week. This is a high-impact role for someone who enjoys working close to engineering, shaping internal platforms and enabling teams to deliver software efficiently, securely and at scale within a global airline and technology environment. If this resonates with your profile, feel free to reach out. Agap2 es una empresa que ofrece igualdad de oportunidades, por ello nos comprometemos a tratar todas las candidaturas por igual en función de sus capacidades, logros y experiencia. Animamos a cualquier persona a presentar su candidatura que será tratada con igualdad de oportunidades independientemente de su raza, nacionalidad, sexo, edad, discapacidad, orientación sexual, identidad de género o cualquier otra característica.

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. POSITION OVERVIEW ICFO is seeking a Procurement Technician to support the operational deployment of the PIXEurope pilot line. The selected candidate will be responsible for managing the procurement needs of the project – including public tenders, orders, deliveries, and associated documentation – and providing basic legal counsel support to ensure that contracts and agreements are properly executed. The Procurement Technician will work closely with the Pilot Line Procurement and Financial Manager, the technical staff to establish requirements and provide procurement and legal guidance, and the Director of the Strategic Initiative. The role will also involve close collaboration with ICFO’s Legal Team, Projects Financial Control Team, and Finance Team. The position will operate under the supervision of the Legal Team – particularly the procurement staff – who will ensure that all activities are carried out in full alignment with ICFO’s internal procedures and compliance requirements. KEY RESPONSIBILITIES • Manage all phases of procurement procedures for the PIXEurope pilot line, from planning and tender preparation to delivery and invoicing., • Work with technical staff to define requirements, advise on procurement options, and ensure timely acquisition of goods and services., • Prepare and publish tender documents in compliance with public procurement regulations and ICFO’s internal policies., • Coordinate the evaluation of offers and preparation of contractual and administrative documentation., • Liaise with suppliers, project partners, and internal stakeholders to ensure timely and accurate execution of procurement processes., • Maintain accurate and organized procurement and contractual records in both physical and electronic formats., • Provide the Pilot Line with basic legal counsel support, including reviewing and preparing project-related contracts, agreements, and memorandums of understanding., • Support in audits and financial justification for public/European funding. QUALIFICATIONS AND EXPERIENCE REQUIRED The ideal candidate will bring: • A university degree in Law, Business Administration, Political Science, or a related discipline., • At least 2 years of experience in public procurement or contract management, ideally in the public sector or a research environment., • Knowledge of the Spanish Public Sector Contracts Law and procurement procedures., • Fluency in English, Spanish, and Catalan (written and spoken)., • Strong organizational, communication, and problem-solving skills., • Proficiency with office and collaborative tools (e.g., MS Office, Teams, SharePoint). Additional skills and experience that will be valued: • Knowledge of legal counsel functions in a project-based environment., • Experience in procurement of scientific or technical equipment., • Familiarity with EU-funded projects (e.g., Horizon Europe, Chips JU) – valued but not required., • Experience in process optimization and continuous improvement of procurement tools and workflows. WHAT WE OFFER • Indefinite contract for scientific and technical activities pursuant to Spanish Law 14/2011, linked to the duration of the Pilot Line initiative., • A unique opportunity to shape and drive a high-impact European initiative at the forefront of photonic innovation., • Integration into a vibrant, international, and multidisciplinary environment at ICFO., • Integration into ICFO’s vibrant, multidisciplinary, and international research community., • A strategic position in a project that will define the future of European photonics., • A competitive salary according to ICFO’s internal scales and a family allowance, if applicable, in line with institutional policy. APPLICATION PROCESS To apply, please submit your resume, a cover letter outlining your experience and contact information for two professional references. Applications should be submitted via LinkedIn or the ICFOjobs platform Selection will include a pre-screening of applicants based on eligibility and experience, followed by an interview with a short-list of candidates. Candidates will be notified of the outcome within 15 days of the interview. 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 PIXEurope is co-funded by the Chips Joint Undertaking and national funding authorities of the Participating States, Spain, Ireland, The Netherlands, Finland, Belgium, Portugal, Poland, Austria , France, Italy, United Kingdom. In particular, it is co-funded by Spain through the Ministry for Digital Transformation and Civil Service under reference CJU-010000-2025-0005, as part of the Recovery, Transformation and Resilience Plan (PRTR).

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. POSITION OVERVIEW ICFO is seeking a Procurement Technician to support the operational deployment of the PIXEurope pilot line. The selected candidate will be responsible for managing the procurement needs of the project – including public tenders, orders, deliveries, and associated documentation – and providing basic legal counsel support to ensure that contracts and agreements are properly executed. The Procurement Technician will work closely with the Pilot Line Procurement and Financial Manager, the technical staff to establish requirements and provide procurement and legal guidance, and the Director of the Strategic Initiative. The role will also involve close collaboration with ICFO’s Legal Team, Projects Financial Control Team, and Finance Team. The position will operate under the supervision of the Legal Team – particularly the procurement staff – who will ensure that all activities are carried out in full alignment with ICFO’s internal procedures and compliance requirements. KEY RESPONSIBILITIES • Manage all phases of procurement procedures for the PIXEurope pilot line, from planning and tender preparation to delivery and invoicing., • Work with technical staff to define requirements, advise on procurement options, and ensure timely acquisition of goods and services., • Prepare and publish tender documents in compliance with public procurement regulations and ICFO’s internal policies., • Coordinate the evaluation of offers and preparation of contractual and administrative documentation., • Liaise with suppliers, project partners, and internal stakeholders to ensure timely and accurate execution of procurement processes., • Maintain accurate and organized procurement and contractual records in both physical and electronic formats., • Provide the Pilot Line with basic legal counsel support, including reviewing and preparing project-related contracts, agreements, and memorandums of understanding., • Support in audits and financial justification for public/European funding. QUALIFICATIONS AND EXPERIENCE REQUIRED The ideal candidate will bring: • A university degree in Law, Business Administration, Political Science, or a related discipline., • At least 2 years of experience in public procurement or contract management, ideally in the public sector or a research environment., • Knowledge of the Spanish Public Sector Contracts Law and procurement procedures., • Fluency in English, Spanish, and Catalan (written and spoken)., • Strong organizational, communication, and problem-solving skills., • Proficiency with office and collaborative tools (e.g., MS Office, Teams, SharePoint). Additional skills and experience that will be valued: • Knowledge of legal counsel functions in a project-based environment., • Experience in procurement of scientific or technical equipment., • Familiarity with EU-funded projects (e.g., Horizon Europe, Chips JU) – valued but not required., • Experience in process optimization and continuous improvement of procurement tools and workflows. WHAT WE OFFER • Indefinite contract for scientific and technical activities pursuant to Spanish Law 14/2011, linked to the duration of the Pilot Line initiative., • A unique opportunity to shape and drive a high-impact European initiative at the forefront of photonic innovation., • Integration into a vibrant, international, and multidisciplinary environment at ICFO., • Integration into ICFO’s vibrant, multidisciplinary, and international research community., • A strategic position in a project that will define the future of European photonics., • A competitive salary according to ICFO’s internal scales and a family allowance, if applicable, in line with institutional policy. APPLICATION PROCESS To apply, please submit your resume, a cover letter outlining your experience and contact information for two professional references. Applications should be submitted via LinkedIn or the ICFOjobs platform Selection will include a pre-screening of applicants based on eligibility and experience, followed by an interview with a short-list of candidates. Candidates will be notified of the outcome within 15 days of the interview. 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 PIXEurope is co-funded by the Chips Joint Undertaking and national funding authorities of the Participating States, Spain, Ireland, The Netherlands, Finland, Belgium, Portugal, Poland, Austria , France, Italy, United Kingdom. In particular, it is co-funded by Spain through the Ministry for Digital Transformation and Civil Service under reference CJU-010000-2025-0005, as part of the Recovery, Transformation and Resilience Plan (PRTR).

Do you dream of working in a company that is driven by a meaningful purpose? An inclusive company that empowers you to do your best and be innovative? Discover the opportunity to join an international, dynamic, and responsible company that fosters the development of all its people around the world. Every day, we empower employees to achieve more and experience exciting careers. Find out how our values and unique position make Schneider Electric a top 25 employer of choice, according to LinkedIn. Join Schneider Electric and power your career! As a global specialist in Energy Management with operations in more than 100 countries, Schneider Electric offers integrated solutions across multiple market segments, including leadership positions in Utilities & Infrastructures, Industries & Machine Manufacturers, Non-residential Buildings, Data Centers & Networks and Residential. Focused on making energy safe, reliable, efficient, productive and green, the company’s 130,000 plus employees achieved sales of about 25 billion EUR in 2020, through an active commitment to help individuals and organizations make the most of their energy. The Mid Level Electrical Project Engineer is responsible for understanding the technical requirements of the project. He or she shall thoroughly understand the design documents, specifications, references, and project scope. The Senior Project Engineer’s role includes coordinating and preparing all technical documentation to build a prefab solution according to customer requirements within time schedule and the defined quality. Strict attention to detail, understanding of time constraints, and implications of proper documentation all add up to an effective Senior Project Engineer. As part of the engineering team the Project Engineer will be working closely with Project Managers, Technical Leaders, Junior Project Engineers and Production Specialist (Factories), this position is responsible for the technical portion of projects at execution stages. What will you do? • Thoroughly understand the design documents, specifications, references, and project scope., • Keep minutes for all regular and technical design meetings., • Identify, review, collect, verify and store all project technical documents as they are available during the project., • Maintain the general project files according internal procedures (Autodesk Construction Cloud, Sharepoint etc…), • Maintain the Engineering issues Log & Project Engineer Book. (Sharepoint folder), • Develop Approval drawings to meet customer scope (Submittal Package), • Perform change management for design documents and customer submittals, • Track all technical design deviations and notify project/ design team for resolution., • Manage all engineering works schedule and assign tasks to designers and SME’s. (specialists), • Develop major BOM (Bill of Material) for the project., • Coordinate internal periodic design reviews with designers and SME’s (Execution phase), • Create and distribute submittal requests based on project requirements., • Maintain and track submittals and shop drawings, • Maintain and track engineering hours budget., • Maintain current design documents with all addenda and redlines., • Perform QC during the integration phase to ensure compliance with design documents., • Manage handover of all engineering documentation to Factory Production Specialists, • Prepare all final documentation for the project including (as built drawings, certificates, O&M documents, Spare Part lists), • Secure all warranties and guarantees from subcontractors and vendors as defined in the design documents, specifications, and contract., • Ensure all changes to the design documents are redlined to manage the final as-built documents. General duties include: • Coaching Junior Project Engineers during large or complex projects while working together in a customer project, • Working with Technical Leaders or Project Managers to deliver technical information to customer on time., • Working with Factory Production Specialist to resolve questions during the execution of the project, • Establishing, maintaining, conducting, and policing detailed procedures for the submittal review, coordination, approval, and distribution of shop drawings, samples, etc., • Establishing and maintaining all Project Engineering files related to subcontract and bid package records, plans, specifications, changes, clarifications, and as-built documents. About you What qualifications will make you successful? • Education University Bachelor’s degree in Engineering Programs (Electrical or Mechanical Engineering are preferred) Experience (not mandatory but very valuable): Data Center critical infrastructure knowledge (Power, Cooling, Monitoring) Building construction or industrial installations (Cabling, lighting, piping, plumbing) • Skills The following skills apply to this position: Coordinate for project documentation from electrical, mechanical, plumbing, architectural, and structural discipline to meet customer requirements and production constraints. Working with other team members, Technical Leaders, contractors/vendors and consultants to resolve technical issues and to ensure the quality and integrity of engineering design executions. Optimizing designs in compliance with relevant regulatory codes, standards and best practices. Proven skills in written and oral communication of technical information. Excellent communication, organization and teamwork skills with the ability to pay a high level of attention to detail. Capacity to work under pressure in order to meet deadlines. Functional knowledge using Microsoft Office suite, Autodesk REVIT, Autodesk Construction Cloud , AutoCAD 2D and Adobe Acrobat Pro. Experience working in REVIT (preferred) Fluent in English If you would like to have: • Exciting job in an international company, with opportunities to lead and contribute to different projects & actions (e.g. CSR, charity, Employer Branding, Well-Being), • Work in a diverse and supportive team of professionals, • Buddy, mentor & induction training - that will help you to smoothly find yourself in our company, • Special training tailored to your needs and career goals, • No formal dress code - we welcome people as they are and perceive diversity as value for the company, • Possibility to use foreign languages and to collaborate with cross-region teams ...share your CV (in English) with us. At Schneider Electric, we believe access to energy and digital is a basic human right. We empower all to do more with less, ensuring Life Is On everywhere, for everyone, at every moment. We provide energy and automation digital solutions for efficiency and sustainability.

Como Legal & Compliance Specialist serás responsable de impulsar y dar soporte al día a día del departamento Legal, con especial foco en la gestión y revisión de contratos, garantizando que todas las operaciones se desarrollen conforme a la normativa vigente. Además, participarás activamente

At Rob Surgical we are looking to hire a Process Engineering Quality Assurance Technician to join our Quality team and support the continuous improvement and validation of our manufacturing and quality processes. 🧬 About us We are a healthtech company specialized in the development of advanced robotic systems for high-precision minimally invasive surgery. Founded in 2012 as a spin-off from UPC and IBEC, our mission is clear: to make robot-assisted surgery more accessible, precise, and efficient worldwide. 🔍 What will your mission be? As a Process Engineering QA Technician, you will play a key role in ensuring the effectiveness of our Quality Management System (QMS) by supporting the validation master plan, calibration program, and process quality activities. You will work closely with product managers, project managers, developers, and manufacturing teams to ensure quality and regulatory compliance across the entire product lifecycle. 🛠 Your main responsibilities will include: Quality Management System • Drafting and reviewing documentation related to QMS processes., • Participating in the maintenance of risk analyses for QMS processes., • Monitoring and maintaining quality KPIs., • Conducting regular inspections in the production plant to verify process control and compliance with procedures., • Organizing and participating in quality meetings., • Supporting the transfer from design to production, including control plans and control methods., • Training manufacturing personnel when required., • Supporting the design and construction of test rigs for design and manufacturing validation., • Writing validation protocols and reports., • Participating in validation execution and monitoring progress of the validation plan., • Preparing validation maintenance reports and monitoring equipment, facilities, and services., • Participating in validations related to:, • Clean rooms, • Ethylene oxide and wet steam sterilization systems, • Computerized systems, • Analytical test methods, • Maintaining and updating facility and process risk analyses., • Monitoring the calibration program and reporting progress., • Developing and updating calibration procedures., • Participating in calibration activities and issuing calibration reports., • Supporting internal and external audits., • Collaborating in the preparation of annual R&D reports and department budgets., • Supporting administrative tasks related to documentation, digitalization, and archiving., • Contributing to maintaining an organized and efficient work environment. 🎓 What are we looking for? • Bachelor’s degree in Industrial Engineering is highly valued., • Experience level: 3+ years of experience, • Experience in medical devices and/or pharmaceutical industry is highly valued., • Professional working proficiency in English., • Advanced Microsoft Office user., • Experience working with ERP environments. 📚 Valuable knowledge Experience or training related to: • ISO 17025 – Calibration laboratories, • ISO 14644 – Clean rooms, • ISO 11135 / ISO 14937 – Sterilization of medical devices, • ISO 14971 – Risk management for medical devices, • GAMP5 – Validation of computerized systems, • GMP and validation regulations, • Metrology or microbiology 💡 We are looking for someone who is… • Detail-oriented but able to understand the big picture., • Analytical, proactive, and collaborative., • Meticulous, organized, and efficient., • A strong communicator with teamwork. 🎯 What do we offer? • Full-time permanent contract., • Salary aligned with profile and experience., • Flexible working hours., • Monthly fruit and vegetable box 🍎, • Opportunity to work on cutting-edge surgical robotics technology., • Professional development in a highly innovative and regulated environment., • A dynamic and collaborative team where your work has real impact on patients’ lives.

At Rob Surgical we are looking to hire a Process Engineering Quality Assurance Technician to join our Quality team and support the continuous improvement and validation of our manufacturing and quality processes. 🧬 About us We are a healthtech company specialized in the development of advanced robotic systems for high-precision minimally invasive surgery. Founded in 2012 as a spin-off from UPC and IBEC, our mission is clear: to make robot-assisted surgery more accessible, precise, and efficient worldwide. 🔍 What will your mission be? As a Process Engineering QA Technician, you will play a key role in ensuring the effectiveness of our Quality Management System (QMS) by supporting the validation master plan, calibration program, and process quality activities. You will work closely with product managers, project managers, developers, and manufacturing teams to ensure quality and regulatory compliance across the entire product lifecycle. 🛠 Your main responsibilities will include: Quality Management System • Drafting and reviewing documentation related to QMS processes., • Participating in the maintenance of risk analyses for QMS processes., • Monitoring and maintaining quality KPIs., • Conducting regular inspections in the production plant to verify process control and compliance with procedures., • Organizing and participating in quality meetings., • Supporting the transfer from design to production, including control plans and control methods., • Training manufacturing personnel when required., • Supporting the design and construction of test rigs for design and manufacturing validation., • Writing validation protocols and reports., • Participating in validation execution and monitoring progress of the validation plan., • Preparing validation maintenance reports and monitoring equipment, facilities, and services., • Participating in validations related to:, • Clean rooms, • Ethylene oxide and wet steam sterilization systems, • Computerized systems, • Analytical test methods, • Maintaining and updating facility and process risk analyses., • Monitoring the calibration program and reporting progress., • Developing and updating calibration procedures., • Participating in calibration activities and issuing calibration reports., • Supporting internal and external audits., • Collaborating in the preparation of annual R&D reports and department budgets., • Supporting administrative tasks related to documentation, digitalization, and archiving., • Contributing to maintaining an organized and efficient work environment. 🎓 What are we looking for? • Bachelor’s degree in Industrial Engineering is highly valued., • Experience level: 3+ years of experience, • Experience in medical devices and/or pharmaceutical industry is highly valued., • Professional working proficiency in English., • Advanced Microsoft Office user., • Experience working with ERP environments. 📚 Valuable knowledge Experience or training related to: • ISO 17025 – Calibration laboratories, • ISO 14644 – Clean rooms, • ISO 11135 / ISO 14937 – Sterilization of medical devices, • ISO 14971 – Risk management for medical devices, • GAMP5 – Validation of computerized systems, • GMP and validation regulations, • Metrology or microbiology 💡 We are looking for someone who is… • Detail-oriented but able to understand the big picture., • Analytical, proactive, and collaborative., • Meticulous, organized, and efficient., • A strong communicator with teamwork. 🎯 What do we offer? • Full-time permanent contract., • Salary aligned with profile and experience., • Flexible working hours., • Monthly fruit and vegetable box 🍎, • Opportunity to work on cutting-edge surgical robotics technology., • Professional development in a highly innovative and regulated environment., • A dynamic and collaborative team where your work has real impact on patients’ lives.

At Rob Surgical we are looking to hire a Process Engineering Quality Assurance Technician to join our Quality team and support the continuous improvement and validation of our manufacturing and quality processes. 🧬 About us We are a healthtech company specialized in the development of advanced robotic systems for high-precision minimally invasive surgery. Founded in 2012 as a spin-off from UPC and IBEC, our mission is clear: to make robot-assisted surgery more accessible, precise, and efficient worldwide. 🔍 What will your mission be? As a Process Engineering QA Technician, you will play a key role in ensuring the effectiveness of our Quality Management System (QMS) by supporting the validation master plan, calibration program, and process quality activities. You will work closely with product managers, project managers, developers, and manufacturing teams to ensure quality and regulatory compliance across the entire product lifecycle. 🛠 Your main responsibilities will include: Quality Management System • Drafting and reviewing documentation related to QMS processes., • Participating in the maintenance of risk analyses for QMS processes., • Monitoring and maintaining quality KPIs., • Conducting regular inspections in the production plant to verify process control and compliance with procedures., • Organizing and participating in quality meetings., • Supporting the transfer from design to production, including control plans and control methods., • Training manufacturing personnel when required., • Supporting the design and construction of test rigs for design and manufacturing validation., • Writing validation protocols and reports., • Participating in validation execution and monitoring progress of the validation plan., • Preparing validation maintenance reports and monitoring equipment, facilities, and services., • Participating in validations related to:, • Clean rooms, • Ethylene oxide and wet steam sterilization systems, • Computerized systems, • Analytical test methods, • Maintaining and updating facility and process risk analyses., • Monitoring the calibration program and reporting progress., • Developing and updating calibration procedures., • Participating in calibration activities and issuing calibration reports., • Supporting internal and external audits., • Collaborating in the preparation of annual R&D reports and department budgets., • Supporting administrative tasks related to documentation, digitalization, and archiving., • Contributing to maintaining an organized and efficient work environment. 🎓 What are we looking for? • Bachelor’s degree in Industrial Engineering is highly valued., • Experience level: 3+ years of experience, • Experience in medical devices and/or pharmaceutical industry is highly valued., • Professional working proficiency in English., • Advanced Microsoft Office user., • Experience working with ERP environments. 📚 Valuable knowledge Experience or training related to: • ISO 17025 – Calibration laboratories, • ISO 14644 – Clean rooms, • ISO 11135 / ISO 14937 – Sterilization of medical devices, • ISO 14971 – Risk management for medical devices, • GAMP5 – Validation of computerized systems, • GMP and validation regulations, • Metrology or microbiology 💡 We are looking for someone who is… • Detail-oriented but able to understand the big picture., • Analytical, proactive, and collaborative., • Meticulous, organized, and efficient., • A strong communicator with teamwork. 🎯 What do we offer? • Full-time permanent contract., • Salary aligned with profile and experience., • Flexible working hours., • Monthly fruit and vegetable box 🍎, • Opportunity to work on cutting-edge surgical robotics technology., • Professional development in a highly innovative and regulated environment., • A dynamic and collaborative team where your work has real impact on patients’ lives.

Como Legal & Compliance Specialist serás responsable de impulsar y dar soporte al día a día del departamento Legal, con especial foco en la gestión y revisión de contratos, garantizando que todas las operaciones se desarrollen conforme a la normativa vigente. Soporte jurídico en proyectos tran

Como Legal & Compliance Specialist serás responsable de impulsar y dar soporte al día a día del departamento Legal, con especial foco en la gestión y revisión de contratos, garantizando que todas las operaciones se desarrollen conforme a la normativa vigente. Soporte jurídico en proyectos tran

Dar soporte administrativo a la red de ventas de la línea Humana.Gestionar procesos de Compliance para Formaciones, Ponencias y Eventos.Realizar el seguimiento administrativo de la actividad de la red de ventas (Información de visitas, clientes, facturación, productos, entre otras).Gestionar los

Dar soporte administrativo a la red de ventas de la línea Humana.Gestionar procesos de Compliance para Formaciones, Ponencias y Eventos.Realizar el seguimiento administrativo de la actividad de la red de ventas (Información de visitas, clientes, facturación, productos, entre otras).Gestionar los

Fresh Del Monte is one of the world's leading vertically integrated producers, marketers and distributors of high-quality fresh and fresh-cut fruit and vegetables, as well as a leading producer and distributor of prepared food across the globe. The Group is established in more than 100 countries and has nearly 40.000 employees worldwide. We are looking for a Key Account Manager based in Castelldefels (Barcelona), on a permanent contract. The Key Account Manager maintain the relationship between key distributors and customers as well as internal sourcing and distribution department. The successful candidate will be responsible for the following tasks: • Validate daily customer orders (ECI, Consum), issue weekly invoicing to customers, and reconcile customer debit/credit notes., • Approve suppliers’ weekly invoices, issue the corresponding packaging invoice, validate weekly production yield, and update related accruals., • Monitor packaging stock levels (pots and resealable film) and issue production write offs., • Review weekly P&L and key KPIs (volume, sales, OI, yield/waste and service level)., • Conduct weekly market checks on pricing, new product launches, and competitor activity. -Define the category strategy, including portfolio development, price positioning, and the innovation roadmap. -Develop new customers and business opportunities. -Lead demand planning, volume forecasting, and the resolution of operational or supply issues to ensure business continuity. -Approve packaging purchases with Corporate Procurement (forecasting, costing). -Ensure packaging availability and cost efficiency through proactive supplier management and forecasting. -Manage POS activities and coordinate with Marketing, Quality, Logistics, Finance, and Procurement. Skills required: • Bachelor’s degree from business school., • Fundamental experience as sales (min. 3/5 years’ experience) with B2B preferably in FMCG company., • Fluent in English., • Managing external relationships with third parties, coordination projects., • Financial acumen. Acknowledgement of financial systems and reporting; planning and forecasting., • Analytical skills: good numeracy, understanding P&Ls, financial reports., • Entrepreneurial., • Strategic thinking: experienced in developing, preparing, and presenting strategic plans and ability to challenge the plans presented by distributor., • Excellent communicational/organizational skills., • IT-experience: ability to create and prepare Power Point presentations, good Excel skills., • Presentation: senior level presentation & communication skills required. Ability to communicate at all levels., • Able to travel across the Region.

Fresh Del Monte is one of the world's leading vertically integrated producers, marketers and distributors of high-quality fresh and fresh-cut fruit and vegetables, as well as a leading producer and distributor of prepared food across the globe. The Group is established in more than 100 countries and has nearly 40.000 employees worldwide. We are looking for a Key Account Manager based in Castelldefels (Barcelona), on a permanent contract. The Key Account Manager maintain the relationship between key distributors and customers as well as internal sourcing and distribution department. The successful candidate will be responsible for the following tasks: • Validate daily customer orders (ECI, Consum), issue weekly invoicing to customers, and reconcile customer debit/credit notes., • Approve suppliers’ weekly invoices, issue the corresponding packaging invoice, validate weekly production yield, and update related accruals., • Monitor packaging stock levels (pots and resealable film) and issue production write offs., • Review weekly P&L and key KPIs (volume, sales, OI, yield/waste and service level)., • Conduct weekly market checks on pricing, new product launches, and competitor activity. -Define the category strategy, including portfolio development, price positioning, and the innovation roadmap. -Develop new customers and business opportunities. -Lead demand planning, volume forecasting, and the resolution of operational or supply issues to ensure business continuity. -Approve packaging purchases with Corporate Procurement (forecasting, costing). -Ensure packaging availability and cost efficiency through proactive supplier management and forecasting. -Manage POS activities and coordinate with Marketing, Quality, Logistics, Finance, and Procurement. Skills required: • Bachelor’s degree from business school., • Fundamental experience as sales (min. 3/5 years’ experience) with B2B preferably in FMCG company., • Fluent in English., • Managing external relationships with third parties, coordination projects., • Financial acumen. Acknowledgement of financial systems and reporting; planning and forecasting., • Analytical skills: good numeracy, understanding P&Ls, financial reports., • Entrepreneurial., • Strategic thinking: experienced in developing, preparing, and presenting strategic plans and ability to challenge the plans presented by distributor., • Excellent communicational/organizational skills., • IT-experience: ability to create and prepare Power Point presentations, good Excel skills., • Presentation: senior level presentation & communication skills required. Ability to communicate at all levels., • Able to travel across the Region.

MEDICAL AFFAIRS Ophthalmology En Salvat buscamos incorporar un perfil de Medical Affairs Ophthalmology, dispuesto a marcar la diferencia. ¿Quiénes somos? Somos Grupo Farmacéutico Salvat, fundada en Barcelona en 1955 y llevamos 70 años contribuyendo a crear una vida más saludable y feliz con productos emblemáticos como Cristalmina, Cetraxal, Monolitum y Salvacolina. 🌍 Presencia internacional. Operamos en + de 60 países, con plantas de producción en Barcelona, Madrid y Miami. 🔧 Innovación y capacidades. Contamos con I+D propia, innovamos y desarrollamos soluciones en las áreas terapéuticas de oftalmología, otorrinolaringología y gastroenterología, además de abordar el ámbito de la salud en Consumer Health y ofrecer servicios CDMO, donde ambicionamos ser un player relevante. 🏅 Excelencia certificada. Estamos orgullosamente certificados por la FDA y reconocidos con calificación excelente en el Plan Profarma del Ministerio de Industria. Esto respalda nuestro compromiso con la excelencia y ética empresarial. 🚀 Proyecto New Salvat. Estamos inmersos en un ambicioso proyecto transformador que busca crear un Salvat más fuerte, más ágil y competitivo. Si te gustan los retos y quieres disfrutar dejando una huella positiva, Salvat es tu lugar. 🤝 Nuestra cultura. Vivimos nuestros valores AACT (Ambición, Accoountability, Colaboración y Transparencia) en el día a día, creemos en el potencial de las personas y fomentamos entornos de donde cada persona pueda crecer y dar su mejor versión. ¿Qué buscamos? El Medical Affairs Ophthalmology será responsable de proporcionar soporte médico-científico en el desarrollo y ejecución de planes médicos en el área de oftalmología. Reportando al Head of Medical Affairs, este rol representa el enlace clave entre las áreas médico-científica y comercial, asegurando la integración de la evidencia clínica y las actividades operativas y estratégicas de la compañía. Tus principales responsabilidades serán: • Soporte Médico-Científico:, • Apoyo médico a los equipos internos, incluidas las áreas de marketing, ventas, (tanto en la elaboración de materiales como en establecer estrategias conjuntas para las diferentes áreas terapéuticas y los diferentes productos), regulatorio (en la elaboración de documentación necesaria) e I+D (en la valoración de posibles proyectos a desarrollar., • Preparar materiales médicos basados en evidencia científica, • Relaciones con KOLs:, • Establecer y mantener relaciones sólidas con líderes de opinión clave y otros profesionales de la salud, • Facilitar reuniones científicas y grupos de discusión para recopilar información del mercado, • Generar proyectos de valor con Sociedades Científicas en el área terapéutica de oftalmología., • Estudios clínicos:, • Apoyar la implementación de ensayos clínicos, estudios observacionales y generación de datos en práctica clínica (RWE), • Colaborar en la revisión y aprobación de protocolos de investigación y publicaciones científicas, • Compliance:, • Garantizar el cumplimiento de la normativa de buenas prácticas en todas en todas las actividades médicas realizadas, • Participar en la formación y capacitación del equipo sobre normativas y buenas prácticas clínicas, • Estrategia médica:, • Contribuir al desarrollo de planes médicos estratégicos alineados con los objetivos de la compañía, • Revisión y análisis de publicaciones científicas / guías de manejo clínico y monitorizar las tendencias en el campo médico relevante, • Patient Advocacy:, • Colaboración estrecha con asociaciones de pacientes para promover un entendimiento profundo de sus necesidades Perfil ideal • Formación universitaria en ciencias de la salud (preferiblemente Medicina, Farmacia o Biomedicina), • Experiencia mínima de 5 años en departamento médico, imprescindible experiencia en el área de oftalmología, • Capacidad de para mediar y construir relaciones con los diferentes stakeholders (internos y externos), • Habilidades de comunicación efectiva, • Dominio del inglés para la implicación en proyectos internacionales Habilidades: Con habilidades técnicas y conocimientos en el área de Medical Affairs (o similar) , buscamos: • Con experiencia en Oftalmología, • con capacidad de Autocrítica,, • Ganas de Superación y de Aprendizaje constantemente, Proactividad,, • Capacidad de esfuerzo y de trabajo,, • Capacidad de búsqueda de soluciones alternativas a las adversidades., • Motivación ¿Qué te ofrecemos? • Formar parte de una empresa sólida e innovadora, en un momento de transformación y crecimiento., • Un entorno colaborativo donde se valora tu iniciativa y tus ideas., • Oportunidades de desarrollo profesional real, participando en procesos clave del área y trabajando bajo estándares GMP., • Paquete de beneficios y aprendizaje continuo en un entorno regulado., • Horario Flexible y jornada intensiva los viernes y en verano. ¿Quieres formar parte de este proyecto transformador? Aplica para más información ¡Vamos a construir juntos el futuro de Salvat!

Career Opportunities: Senior Engineering Manager (Manufacturing) (80801) Senior Engineering Manager - Manufacturing Execution System ( MES) The Company Founded in 1977, Almarai Company is the world’s largest vertically integrated dairy company and the largest food and beverage manufacturing and distribution company in MENA. Headquartered in Riyadh, Almarai Company is ranked as the number one FMCG Brand in the MENA region and the market leader in all its categories across GCC, Egypt, and Jordan. Over five decades of sustainable growth, Almarai has consistently provided nutritious and healthy products to consumers of all ages, driven by its core principle: “Quality you can trust.” Almarai has expanded its product range to include, in addition to dairy products, juices and beverages, baked goods, poultry, infant formula, dates, fish and seafood, and bottled water, under more than 20 brands such as Almarai, L’usine, 7DAYS, ALYOUM, Nuralac, Farm’s Select, Ice Leaf, Almira, Seama, Oska, IVAL, Almarai Pro, Premier Chef, Bakemart, and others. Almarai currently employs over 46,000 Quality Makers, across the GCC, Egypt & Jordan. In 2025, Almarai reported net income of SAR 2.4 billion on sales of SAR 22 billion. An aggressive expansion program together with acquisitions in new vertical markets have created an exciting opportunity to join a dynamic multinational team dedicated to furthering growth plans for the group. The Opportunity Almarai is seeking a highly experienced Senior Engineering Manager – Manufacturing Execution System (MES) to support the continued digitization and optimization of its manufacturing operations. This role will be responsible for leading the design, implementation, and ongoing enhancement of MES solutions that enable paperless manufacturing, production visibility, system integration, and operational excellence across multiple manufacturing sites. The successful candidate will act as the bridge between manufacturing, quality, engineering, and IT teams, ensuring MES platforms are aligned with business goals and plant requirements. The role will lead MES deployments and upgrades, manage system integrators and technology partners, and ensure robust integration with automation systems. A strong focus will be placed on standardization, scalability, compliance, and long ‑ term sustainability of MES solutions while supporting plant operations through stable and well ‑ validated systems. Qualifications: Bachelor’s degree in IT / Computer Science, Engineering, or a related technical discipline. Minimum 7 years’ experience in Manufacturing Execution Systems (MES), MOM, or digital manufacturing – preferably, pharmaceutical, food or dairy processing. Experience within FMCG, food & beverage, pharmaceutical, or regulated manufacturing environments Hands‑on experience with MES platforms such as Siemens Opcenter (Execution / Pharma / Discrete), SIMATIC IT, Camstar, or similar Experience interfacing MES with automation systems, historians (e.g., OSI PI), OPC, and third ‑ party applications Familiarity with system validation, data integrity, and manufacturing standards (e.g., GAMP 5, 21 CFR Part 11, ISA ‑ 95 / ISA ‑ 88) If you meet the qualifications and are looking for a challenging opportunity in a dynamic industry, please apply now. We offer competitive salary and benefits package for the right candidate. We look forward to welcoming you to our team. Apply now and take the next step in your career as a Senior Engineering Manager. #J-18808-Ljbffr

A leading aerospace company in Spain is looking for a Supplier Quality Engineer (SQE) specializing in composite materials. The role entails overseeing supplier quality, conducting audits, and ensuring compliance with material certifications. Candidates should have a bachelor's degree in a relevant field and 3-5 years of experience in Supplier Quality Engineering. The position requires up to 50% travel to suppliers for direct oversight and process verification, with a strong focus on continuous improvement and risk management. #J-18808-Ljbffr

Una compañía farmacéutica busca un Director de Ventas Nacional para liderar la estrategia comercial y asegurar el crecimiento de las ventas en España.El candidato ideal debe tener más de 5 años de experiencia en desarrollo comercial en la industria farmacéutica y un profundo conocimiento del

GP Pharm es una compañía farmacéutica fundada en el año 2000 en Barcelona, su planta farmacéutica está ubicada en Sant Quintí de Mediona (Alt Penedès). La compañía está especializada en productos inyectables que incluyen sistemas de liberación prolongada de fármacos basados en microesferas, liposomas y nanopartículas lipídicas. Nuestras principales áreas terapéuticas de interés son la Oncología, la Urología y la Salud de la Mujer. El National Sales Director es responsable de la dirección, planificación e implementación de la estrategia comercial y de acceso al mercado a nivel nacional. Su objetivo es asegurar el crecimiento sostenido de las ventas, la rentabilidad y el posicionamiento de los productos farmacéuticos de la compañía, garantizando el estricto cumplimiento normativo en todas las operaciones. I. Responsabilidades Clave y Estrategia Definición de la Estrategia Nacional: Diseñar e implementar el Plan Comercial Nacional anual, estableciendo los objetivos de ventas, cuota de mercado y rentabilidad para cada línea de producto y territorio. Gestión del Acceso al Mercado: Colaborar estrechamente con el equipo de Regulatorio y Medico para asegurar la inclusión, el precio y el reembolso de los productos en las guías clínicas, formularios hospitalarios y sistemas de salud regionales/nacionales. Análisis y Proyección: Realizar un análisis profundo del entorno sanitario, de la competencia (incluyendo genéricos/biosimilares) y las tendencias regulatorias para anticipar riesgos y oportunidades. Liderazgo de Cuentas Clave: Supervisar la estrategia enfocada en hospitales, grupos de compra, instituciones sanitarias, mayoristas y decisores clave (KOLs - Key Opinion Leaders) a nivel nacional. II. Gestión y Liderazgo de Equipos Dirección de la Red de Ventas: Liderar, dirigir y motivar al equipo de ventas (equipo de 15 personas) - Gerentes Regionales, Delegados de Ventas y personal de soporte- para alcanzar y superar los objetivos establecidos. Formación y Desarrollo: Implementar programas de formación técnica y científica continuos, así como asegurar el coaching en habilidades de venta y el estricto cumplimiento del Código de Conducta y normativas de Compliance. Asignación de Recursos y Territorios: Gestionar eficientemente la estructura del equipo, la asignación de recursos y la segmentación geográfica para optimizar la cobertura y el impacto. Evaluación del Rendimiento: Establecer KPIs (Indicadores Clave de Desempeño) claros, realizar revisiones de desempeño periódicas y administrar el sistema de incentivos y remuneración del equipo. III. Control Financiero y Cumplimiento Gestión Presupuestaria: Elaborar, gestionar y controlar el presupuesto de ventas y los gastos comerciales y promocionales, garantizando la optimización de los recursos. Previsiones de Venta (Forecasting): Supervisar la precisión de las previsiones de ventas a corto, medio y largo plazo para asegurar una correcta planificación de la producción y la cadena de suministro. Garantía de Compliance: Ser el máximo responsable de asegurar que todas las actividades comerciales se realicen dentro del marco legal y ético, manteniendo la integridad en la interacción con profesionales sanitarios y autoridades. Experiencia: Mínimo 5 años de experiencia probada en posiciones de dirección comercial en la industria farmacéutica, con experiencia directa en la gestión de equipos de ventas nacionales o regionales. Conocimiento Técnico: Profundo conocimiento del Sistema Nacional de Salud (SNS) español, sus procesos de compra, financiación y acceso a medicamentos. Sólidas habilidades de liderazgo estratégico y negociación a alto nivel. Orientación a resultados y alto nivel de ética profesional . Excelentes habilidades de comunicación y presentación. Información adicional: Ubicación: Hospitalet de Llobregat (con disponibilidad para viajar a nivel nacional) Salario fijo + variable por objetivos + retribución en especie #J-18808-Ljbffr

Una empresa de servicios industriales en Cataluña busca un/a Técnico/a de Medio Ambiente para supervisar obligaciones ambientales en instalaciones industriales.A continuación, encontrará un desglose completo de todo lo que se requiere de los posibles candidatos, así como la forma de presentar s

Una empresa farmacéutica busca un Director Nacional de Ventas con experiencia para implementar la estrategia comercial y asegurar el crecimiento sostenido de las ventas en el mercado nacional.Es usted el candidato adecuado para esta oportunidad? Asegúrese de leer la descripción completa a continu

Una firma internacional de servicios profesionales busca incorporar a un contable fiscal junior para apoyar en la contabilización y cierre de informes contables, así como en la preparación y presentación de cuentas anuales.Haga clic en "Solicitar" a continuación para enviar su candidatura.Aseg�

Una empresa de servicios en Cornellà de Llobregat busca un Legal & Compliance Specialist.

The Senior Legal Counsel will be responsible for providing compliance support regarding regulations relevant to the operations and conduct of Bunge’s business globally. The role requires providing decision-making support and advice to the business regarding "grey areas" where there is no clear leg