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At Xiromed, we are committed to making high-quality, affordable medicines accessible to patients across Europe. Operating in a dynamic and international environment, we work cross‑functionally with internal teams and external partners to bring new products to market efficiently, reliably, and in line with the highest quality and regulatory standards. We are looking for a Launch Specialist to support the launch of Xiromed’s EU portfolio pipeline. This role will be responsible for planning, coordinating, and executing launch activities across multiple markets, ensuring that each launch is technically prepared, aligned with business goals, and delivered on time. You will play a key role in maximizing launch value and margin across our markets: Sweden, Denmark, Finland, Norway, Iceland, Germany, the Netherlands, the United Kingdom, Italy, and Poland. • Lead new launch projects and strategic initiatives linked to new commercial opportunities., • Lead dose dispense projects across Europe and help define the best strategy for hospital and retail launches., • Coordinate cross‑functional activities with Business Development, Supply, Logistics, Regulatory, Design, Commercial, IP, Pharmacovigilance, and QA/QC., • Work closely with commercial teams to ensure prioritization is up to date and business needs are clearly understood., • Help define the best launch strategy for each product, including pricing and market access considerations., • Identify risks, opportunities, and process improvement areas, while exploring new sectors and growth opportunities., • Collaborate with internal and external partners to coordinate launch activities and ensure all requirements are completed on time for product supply., • Lead portfolio optimization activities, including pack size optimization, COGs reduction, manufacturing improvements, and logistics improvements., • Maintain and regularly update the overall launch plan, reporting progress and status to relevant stakeholders., • Maintain databases in SAP, IBP, and CRM., • Ensure MMDD maintenance for serialization purposes., • Collaborate with all involved functions to ensure launches are produced according to information approved by Health Authorities., • For products with aRMMs, ensure distribution is completed effectively before launch., • Align with Logistics and QA to ensure appropriate transport conditions are in place and that required agreements and audits are completed., • Bachelor’s degree in Pharmacy, Chemistry, Biotechnology, Industrial Engineering, or a related field., • Previous experience in pharmaceutical launches, project coordination, or cross‑functional roles within the pharma industry., • Experience in the pharmaceutical industry, ideally in product launches, project management, supply, regulatory, quality, or related cross‑functional environments., • Strong understanding of launch planning and cross‑functional coordination in a regulated environment., • Knowledge of GxP/GMP and pharmaceutical regulatory requirements., • Experience working with internal and external stakeholders across different markets., • Familiarity with pricing, market access, supply chain, logistics, and commercial launch strategy will be considered a strong plus., • Experience with SAP, IBP, CRM, and Excel., • Strong project management and coordination skills., • Ability to identify risks, solve problems, and manage multiple priorities at the same time., • Structured way of working, with strong attention to detail and execution., • Strong communication and stakeholder management skills., • Professional level of English, both written and spoken., • Ability to work effectively in an international and cross‑functional environment., • Flexible working hours., • Learning and development opportunities., • A key role with high visibility and real business impact., • The opportunity to contribute to the launch of medicines that improve patients’ access to treatment. At Xiromed, we are committed to building an inclusive workplace where everyone is treated with respect and given equal opportunities. We welcome applications from all qualified candidates regardless of gender, gender identity or expression, age, ethnic or social background, nationality, religion, sexual orientation, disability, or any other protected characteristic. #J-18808-Ljbffr

Experience: 2 to 4 years in similar roles. INSUD PHARMA operates throughout the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to both human and animal health. INSUD PHARMA’s activity is structured into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with more than 9,000 professionals in over 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and over 35 pharmaceutical subsidiaries, serving 1,150 clients in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Are you ready to be a #Challenger? • Provide technical and scientific support for NME and complex generic development projects, driving appropriate biopharmaceutical assessment and contributing to the selection of formulation prototypes., • Identify relationships between drug substance properties, dosage forms, drug release, and drug absorption., • Build mathematical models describing formulation effects on drug absorption (IVIVC and PBPK models)., • Develop predictive PK models based on in vitro dissolution data (IVIVC)., • In collaboration with other team members, develop PK/PD models to address questions related to complex generic products., • Contribute to the implementation of new tools and solutions to strengthen in vitro–in vivo relationships within the department., • Author, review, and contribute to scientific documentation and technical reports to support regulatory submissions (including scientific advice packages and responses to deficiency letters)., • Interact and collaborate scientifically with internal cross-functional project teams and external partners., • Maintain compliance with internal SOPs, regulatory guidelines (ICH, EMA, FDA), and GCP/GLP quality standards., • University degree in Pharmacy, Bioinformatics, Biopharmaceutics, or other related sciences., • PhD in data modeling or related field is a plus., • Strong background in pharmacokinetics and IVIVC., • Knowledge of in vitro dissolution testing (biorelevant/biopredictive API and formulation testing)., • Hands-on experience with programming languages such as R or Python., • Experience with pharmacometric and PBPK platforms such as Phoenix, NONMEM, Simcyp, GastroPlus, PK-Sim, or equivalent tools., • High level of English (spoken and written)., • Intermediate level of Spanish. Flexible entry schedule from Monday to Friday (full-time, 40 hours). Attractive salary package. Benefits & Savings Club. Development plans, internal mobility policy. And many more! Stay alert to your phone and email! Most likely, the first thing we will do is contact you through one of these channels. Get ready! We will continue with an in-person/virtual interview depending on availability and as we agree; the process may include one or two interviews, and depending on the type of process, there may also be some sort of test. Wait for the result! We care that in each selection process you feel guided and know what to expect from us, so we will try to inform you about the status of the process at all times. Follow us on social media like LinkedIn/Instagram and stay tuned for any openings we post: the opportunity to become a new Insuder is waiting! The InsudPharma group is aware that business management must be in harmony with the needs and demands of society, and therefore undertakes a commitment to equal opportunity and treatment between men and women, as set out in current regulations—Organic Law 3/2007—and we do not discriminate against anyone based on ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance. #J-18808-Ljbffr

Técnico/a de soporte informático Se busca personal para integrarse en un equipo de soporte informático internacional. Las funciones principales incluyen la atención a clientes en Emiratos Árabes Unidos y Alemania, con participación en reuniones con los responsables del proyecto. También se trabajará con la plataforma CRM Salesforce para analizar y debatir nuevas funcionalidades, además de utilizar herramientas como Gitlab y metodologías Kanban y Agile. Se requiere experiencia en MongoDB y en la optimización de bases de datos. Los candidatos deben contar con el Bachillerato finalizado, siendo un plus tener un Título Superior en Administración de Sistemas Informáticos. Es indispensable un nivel de inglés A2, y se valorarán conocimientos de francés o árabe en el mismo nivel. Se ofrece un contrato indefinido y jornada completa, con horario de 8 horas diarias, preferiblemente de 06:00 a 15:00, adaptable según el cliente. El salario bruto mensual es de 2.009 euros, con prorrata incluida.

GRUPO HERME es un grupo industrial ubicado en Casarrubuelos (Madrid) con más de 25.Tareas El puesto consiste, entre otras tareas, en la recepción y ubicación de mercancías, preparación de pedidos así como mantenimiento del almacén.Requisitos Es presiso tener experiencia en el manejo de carr

Empresa ubicada en Casarrubuelos(Madrid) precisa Carpintero con experiencia en fabricación y ensamblaje de muebles.Tareas Las tareas a realizar serán: - Manejo de la maquinaria de producción: Escuadradora, canteadora, máquina de corte.Se valorarán conocimientos en lacado de muebles Requisitos