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Our company Archroma is a global diversified leader in specialty chemicals with operations in 42 countries, including 35 sites, all certified to ISO management system standards. With the industry’s broadest product portfolio, we serve many of the world top companies in textiles, packaging and paper, paints and coatings. Headquarter in Pratteln, Switzerland, our team of 5,000 passionate professionals offers industry-leading expertise in manufacturing, technical support and innovation around the globe. Archroma is paving the way to a more sustainable future and is recognized as an industry leader in the development and delivery of sustainable solutions by our customer base. We are known for our advancements in processing technologies and for the introduction of innovative tools that further support partners to save resources while improving productivity and efficiency. Archroma operates as two distinct divisions, our Textile Effects division serving the textile industry with innovative and differentiated products and the Paper Technologies (PT) division which offers unique, sustainable chemistry to the paper, packaging, construction, and paints & coatings industries. Our people Our people have a rich tradition of working alongside our customers as long-term partners and trusted advisors, developing tailored solutions that help customers deliver business success. The diversity of our workforce combined with a commitment to a performance-driven and collaborative culture means our people display a passion and commitment to excellence and innovation that is unmatched. Our people create specialized product solutions that deliver unique economic and environmental benefits to our customers which forms the basis of our long-standing customer relationships. Our people are proud to be part of the journey of leading our industry towards a more sustainable future for our customers and markets...it’s in our nature! Job Description: For our Global Planning team – Textile Effects Division we are looking for a highly motivated and proactive team member in the function of Supply Planner Responsible for weekly planning process for all materials for the assigned plant; inventory management; and critical materials and bottleneck management. This is a permanent and full-time position to be based in Castellbisbal – Barcelona Key Job Responsibilities: 1. Weekly planning: • Own the weekly planning process at SKU level for plant materials within the monthly SIOP cycle., • Ensure accurate replenishment planning from production plant to warehouse. 2. Material Replenishment: • Act as Process Owner for MRP across the region for assigned plant products., • Execute weekly release processes to align stock levels with forecasted demand, open orders, and available inventory., • Ensure accurate stock projections and coverage at month-end., • Oversee proper distribution to warehouses. 3. Inventory Management: • Manage inventory within the Planning scope, reacting to demand deviations and ensuring service level agreements are met., • Responsible for stock levels across all plants (SKU level). 4. Critical Materials: • Optimize identification of critical materials., • Communicate expected shortages, with mitigation actions in place. 5. Master Data Ownership: • Maintain and validate Master Data, • Run regular sanity checks on Master Data. 6. SIOP Process: • Lead the Monthly Supply Alignment meeting., • Actively contribute to GSA meeting preparation by providing key inputs: supply constraints, inventory analysis, and more. 7. Support strategic projects and contribute to new process development and cross-team consolidation. Education/ Experience / Working Time • Bachelor’s Degree or equivalent experience in Planning/Scheduling in a chemical Industry environment, • 5 years of experience in similar position Desired knowledge and skills: • Deep knowledge and understanding of the SAP Material Master Data., • Strong communication skills, • Team Worker, • Leadership Skill, • Accountability, • Problem solving ability, • Strong analytical and structural skills. Strong excel skills, • English and Spanish fluently written/spoken is a must Others • Own vehicle required, as the location is in an industrial area without direct public transport connections, • UE work permit is required Your application If your background and personal experience fits this profile, please send us your complete application via LinkedIn

Proyecto Participarás en el desarrollo de una plataforma propia (producto SaaS) vinculada a un sistema de algoritmos de inteligencia artificial aplicada al mundo industrial. El core del proyecto está centrado en IA y esta posición se orienta al área de delivery, es decir, la construcción de la plataforma que permite la interacción con el usuario. Se trata de un producto escalable, estructurado y de largo recorrido, en fase de MVP. No es desarrollo para terceros, sino desarrollo interno, donde todos los módulos deben integrarse con el conjunto. Descripción del perfil Buscamos un/a Full Stack Developer con foco en Front-End . Perfil senior, con autonomía en el desarrollo. Capacidad de trabajo con enfoque de producto y escalabilidad. Que entienda la importancia de la calidad del código, la modularidad y la integración continua Experiencia en Scrum. Experiencia previa en plataformas SaaS valorada. Tecnologías principales Front-End React con Telerik Kendo UI Back-End con Django Git Jira Requisitos Mínimo 4-5 años de experiencia como desarrollador/a full stack. Capacidad para integrarse de forma rápida en un equipo en fase activa de desarrollo. Se valorará haber trabajado en entornos estructurados y con buenas prácticas de desarrollo. Titulación técnica o experiencia demostrable. Ubicación: Modelo híbrido en Terrassa: Lunes a Miércoles oficina y Jueves y viernes teletrabajo Incorporación: ASAP Jornada: Verano (julio y agosto): intensiva de 8:00 a 15:00 Invierno: 8,5 h de lunes a jueves 6 h los viernes (flexibilidad de entrada entre 8:30 y 9:30)

About Us Based in Barcelona and Treviso, INDIBA Group stands at the forefront of global leadership in Aesthetics, Beauty, Rehabilitation, Sports, Intimate Health, Pharma, and Animal Health solutions, standing on a rich 40-year history of scientific innovation. Our cutting-edge 448 kHz frequency technology is the cornerstone of our world-renowned therapies, empowering individuals to enhance their lives and accelerate recovery from injuries across various sectors. With the integration of K-LASER, a global leader in medical lasers, we’ve propelled our commitment to advancing treatments, embracing new technologies, and expanding our global presence in medical research. Revitalizing lives is what we do and what our teams are working on to achieve daily. What are we looking for? We are looking for a senior leader to oversee the Medical Affairs & Training Department for INDIBA Group. This strategic role combines regulatory and clinical responsibilities with scientific communication and training leadership. The ideal candidate will bring deep medical expertise, strong stakeholder engagement capabilities, and the ability to align and transform clinical insights into business value while supporting company positioning. Which will be your responsabilities? • Lead the development, maintenance, and strategic use of clinical evidence to support product registration and ensure compliance with global medical device regulations., • Oversee the preparation of clinical documentation, including trial protocols, regulatory submissions, and reports to health authorities and notified bodies., • Supervise clinical trials and post-market surveillance, maintaining strong relationships with key opinion leaders (KOLs) and investigators to support research and product positioning., • Act as a key medical representative in audits, inspections, and quality reviews requiring scientific justification or expertise., • Provide scientific support and strategic guidance across internal departments including Commercial, Marketing, R&D, Regulatory and Quality., • Guide the development of scientific materials, publications, and congress contributions to reinforce K-LASER and INDIBA's position in the medical community., • Lead the Training team to ensure delivery of consistent, high-quality programs aligned with the latest clinical data, approved product claims, and corporate objectives., • Monitor emerging clinical trends and innovations to inform product development and positioning., • Ensure the effectiveness of the medical vigilance system in collaboration with relevant departments. What do you need to be a succesful candidate? • Minimum of 10 years’ experience in Pharmaceutical Laboratory, Medical Devices company or regulatory consultancy, in areas such as Medical / Scientific Department, Clinical Research, Medical Writing, Scientific marketing or equivalent., • Experience in writing clinical reports (expert reports, review reports, clinical, pharmacological, pharmacovigilance, phase III / IV studies, or similar) is essential., • Academic background: Degree in Health Sciences (Medicine, Pharmacy, Human Biology or Biomedical Science). Master's or post-graduate studies aimed at the Pharmaceutical, Cosmetic and/or Aesthetic and Rehabilitation Medicine Industry as well cinical trial monitoring will be valued., • Good command of Clinical research methodology., • Fluent Spanish & English language skills in both verbal and written communication. Fluency in another language will be a plus. What we offer? • Full-time and permanent contract., • Location: Sant Cugat del Vallés., • Hybrid work model, • Attractive remuneration package., • Fringe benefits., • Multinational and flexible environment. #J-18808-Ljbffr

Our partner is a company with more than 30 years of experience in developing custom software applications, they have become trusted IT partners in a variety of industries, such as telecommunications, finance, shipping and logistics.Innovative project delivery models and a full stack of different tec