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At ScaleneWorks People Solutions, we're more than recruiters; we're career architects dedicated to connecting exceptional talent with top-tier opportunities. Backed by industry experts, we prioritize relationships, offer global opportunities, and champion your success every step of the way. Ready to shape your future? Explore opportunities with us today. We are looking for a Junior Project Manager for our well-known client. • Location: Barcelona, Spain, • Type of Work: Hybrid, • Employment Type: Permanent About the Role Client’s Digital Go-To-Market (GTM) team is looking for an experienced and detail-oriented Project Manager to support initiatives focused on improving onsite page performance for all Direct to Customer eCommerce stores, marketplaces and Robotic Process Automation (RPA). This role will be instrumental in managing cross-functional projects that enhance our eCommerce operations, improve scalability, and drive digital efficiency across multiple areas of the company. You will work closely with process owners, RPA developers, analysts, and regional stakeholders to deliver high-impact projects, track performance, and ensure seamless execution of digital GTM strategies. You will also focus on improving and continuously optimizing the Google Core Web Vitals for client’s online stores. Key Responsibilities Candidate Profile • Bachelor’s degree in Business, Information Systems, or a related field., • Proven ability to manage multiple projects simultaneously with cross-functional stakeholders., • Strong analytical and problem-solving skills; experience with performance tracking tools or dashboards (e.g., Power BI, Tableau, Excel)., • Excellent communication, organization, and collaboration skills., • PMP or Agile certification is a plus. Ready to Take the Next Step? If you're ready to embark on an exciting journey with ScaleneWorks, we’d love to hear from you! Submit your resume today and let’s unlock new possibilities together KRAZ nr. 28233

The Siegfried Group is a global life science company with a network of 13 sites in Europe, the USA and Asia. Siegfried offers contract development and manufacturing of active pharmaceutical ingredients, intermediates, and drug products and has sales more than CHF 1.3 billion Swiss Franks. Siegfried Holding AG employs over 3,900 people and is listed on the SIX Swiss Exchange (SIX: SFZN). Are you a Senior Manager Business Applications (SAP Data Migration) looking for a new challenge in a dynamic CDMO Pharmaceutical Industry in our Barberà del Vallès site? Reporting to the Head Data Intelligence and SAP-Basis, you will be responsible for replacing the existing system to migrate data, selecting and evaluating data migration designs, governing scalable data migration architectures and standards across SAP programs. Your role: • Technical and functional lead for SAP data migration and master data projects, including architectural transition from R/3 (ECC 6.0) to the S/4HANA landscape., • Convert business needs and design scalable, compliant data migration solutions and roadmaps, ensuring end-to-end consistency and auditability across all Siegfried sites., • Design and govern scalable data migration architectures and standards to ensure quality, compliance, and consistency across SAP programs., • Select and evaluate data migration (e.g., SAP Data Services, LSMW) and master data tools to ensure reusability, compliance, and fit-for-purpose solutions., • Coordination and management of external consulting resources in term of project management, • Conduct internal trainings on data migration and master data, promoting best practices and knowledge sharing. Your profile: • Educational background in Information Technology or equivalent qualification., • Led at least one complex data migration project to SAP S/4HANA., • At least 7 years experience in delivering services related to data migration, transformation, and support for mergers, acquisitions, and divestitures, • Served as an enterprise architect or advisor, guiding customers in building IT roadmaps using SAP products and services., • Experience with Data Management solutions (e.g., MDG, ILM) or SAP Industry Solutions is an added advantage, • Experience with SQL is a plus., • Solution-oriented with strong communication skills., • Willingness to work on a broad range of topics in the area of SAP Master data ., • Resilient team player with high flexibility., • Fluent in Spanish and English, both written and spoken. Working at Siegfried Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs. Who we are In the Midst of People’s Lives – Across the Globe The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.

Como Ingeniero/a de Diseño DSP y FPGA, formarás parte de nuestro equipo global de I+D, contribuye al diseño y la implementación de aplicaciones EAS (Electronic Article Surveillance) destinadas a clientes del sector retail a nivel mundial. Con alto nivel de autonomía, la persona seleccionada trabajará de manera creativa en un entorno orientado al trabajo en equipo para diseñar soluciones, cumplir con los plazos y completar tareas de ingeniería complejas, demostrando plena competencia en tecnologías DSP (Digital Signal Processing) y FPGA (Field Programable Gate Array,) y aplicando estas habilidades a nuestro portafolio de productos. Objetivos y principales responsabilidades: • Contribuir al desarrollo del concepto y diseño de sistemas de hardware e interfaces para todos los proyectos EAS. Las tareas pueden ser a nivel de contribución individual, de equipo o una combinación de ambos., • Investigar soluciones, revisar/analizar, validar/diagnosticar y probar productos., • Debe ser capaz de trabajar en un equipo multifuncional tanto a nivel local como internacional., • Desarrollar requerimientos y presupuestos para funciones de procesamiento de señales., • Ofrecer soporte en simulaciones, implementación y verificaciones de sistemas y FPGA (en MATLAB/Simulink o equivalente)., • Implementar algoritmos DSP en estructuras FPGA., • Realizar evaluaciones de riesgo, proponer y ejecutar estudios de viabilidad, así como orientar en la incorporación de nuevas tecnologías al mercado., • Comunicar de manera oportuna y precisa el estado de los proyectos, ofreciendo ideas alternativas para la resolución de problemas., • Debatir sobre aspectos del diseño, realizar evaluaciones de riesgo, proponer y ejecutar estudios de viabilidad, y ofrecer orientación para la introducción de nuevas tecnologías al mercado., • Contribuir con equipo de innovación, participar de manera sustancial en la planificación de los aspectos técnicos de los proyectos de desarrollo y en su posterior ejecución., • Asumir la responsabilidad de sus entregables juntamente con el equipo, de toda la aplicación. Formación, experiencia y conocimientos: • Ingeniería informática o similar., • Mínimo 5 años de experiencia en roles similares., • Sólida experiencia en diseño DSP y FPGA., • Experiencia en el desarrollo de soluciones de hardware y firmware embebido., • Dominio de lenguajes de programación como C, C++ y HDL (Lenguaje de Descripción de Hardware)., • Conocimiento de MATLAB/Simulink o herramientas de simulación equivalentes., • Inglés fluido; el conocimiento de otros idiomas es un plus. Competencias: • Habilidades para resolver problemas: capacidad para abordar problemas complejos de manera metódica y con pensamiento crítico., • Habilidades de comunicación: capacidad para comunicar conceptos técnicos claramente tanto a miembros técnicos como no técnicos., • Colaboración: experiencia trabajando en equipo y utilizando herramientas como Microsoft Teams, GitHub y Jira., • Adaptabilidad: disposición y capacidad para aprender nuevas herramientas y adaptarse a tecnologías en constante cambio., • Gestión del tiempo: capacidad para manejar múltiples proyectos y cumplir con los plazos de manera eficiente. Qué ofrecemos: • Formarás parte de una empresa multinacional con un buen ambiente laboral y sólidos valores corporativos., • Paquete salarial atractivo y competitivo., • Trabajarás en una empresa dinámica y global, con oportunidades de crecimiento profesional y posibilidades para experimentar y probar nuevas ideas., • Trabajo en modalidad home office dos días a la semana. Residencia en la zona de Barcelona.

Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, mRNA and pDNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, mRNA and pDNA. Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000L, another for microbial and yeast up to 1000L, and a third are for mRNA up to 50L. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do: • Prioritizing customer satisfaction., • Providing cutting-edge end-to-end services., • Utilizing state-of-the-art facilities., • Offering extensive expertise in biologics. We are looking for a new person to join the QA as a Specialist to work in our brand new facilities in Sant Quirze del Vallès: MAIN RESPONSIBILITIES: • To build, with the Head of Quality Assurance oversight, the Quality Management System creating and/or approving Standard Operating Procedures to support GMP manufacturing activities., • To build and manage the Documentation Management System and associated training., • To lead the supplier qualification program, approving new suppliers and managing supplier status during its life cycle., • To review Technical Agreements between the company and suppliers/clients., • To review batch documentation for release purposes., • To support facility, utilities and equipment qualification activities, approving protocols and final reports as well as managing related change control records. REQUIREMENTS: • Bachelor’s degree in a Science field with proven experience in GMP Quality Assurance roles., • In-depth knowledge managing Quality Management Systems (deviations, CAPA, change controls, audits and supplier qualification)., • Experience in batch release activities acting as QP deputy will be a plus., • Experience in facilities, utilities and equipment qualification., • Outstanding problem-solving and decision-making skills., • Team player, excellent verbal and written comunication skills (both Spanish and English) and strong analytical and organizatonal skills.

Leanbio is a leading Biopharmaceutical CDMO offering end-to-end services in the field of recombinant proteins, mRNA and pDNA. With over a decade of expertise, we have a proven track record in development and manufacturing of therapeutic molecules such as antibodies, Fab fragments, ADCs, enzymes, complex proteins, mRNA and pDNA. Leanbio has already worked with over 100 candidates over these years, some already in late clinical stages. Leanbio is expanding its development and manufacturing capabilities with a new GMP site in Barcelona with over 4,000 sqm. and three manufacturing areas: one for mammalian expression systems up to 2000L, another for microbial and yeast up to 1000L, and a third are for mRNA up to 50L. The new facility includes state-of-the-art development laboratories, oustanding Quality control rooms and warehouse. Leanbio is a global service provider for the development and manufacturing of biologics. Our commitment to excellence is evident in everything we do: • Prioritizing customer satisfaction., • Providing cutting-edge end-to-end services., • Utilizing state-of-the-art facilities., • Offering extensive expertise in biologics. We are looking for a new person to join the team as a Marketing Manager in our brand new facilities in Sant Quirze del Vallès: MAIN RESPONSIBILITIES: • Marketing strategy development and execution., • Lead generation and campaign management (digital, events, etc)., • Measure ROI and performance of all marketing activities using KPIs and analytics., • Content Creation & Brand Messaging. Create compelling, scientifically accurate content for web, social media, brochures, whitepapers, case studies, and videos. Maintain brand consistency across all platforms and communications., • Digital Marketing & Website Management., • Plan and manage company participation in events and fairs. Coordinate logistics, branding, promotional material, and follow-up activities with BD. Fairs preparation, assistance and follow-up., • Work creatively and analytically in a problem-solving environment demonstrating teamwork, innovation and excellence., • Market Intelligence & Competitive Analysis: Monitor market trends, customer needs, and competitor positioning in the DS/CDMO space. Provide insights and strategic recommendations to BD and leadership teams., • Business Development Support: develop marketing collateral (presentations, flyers, technical overviews) for the BD team., • Budget & Vendor Management: Manage the marketing budget, external agencies, designers, and other vendors to deliver cost-effective campaigns., • Stakeholder Collaboration: Work closely with internal teams (BD, Technical, PM, Regulatory) to ensure accurate, aligned messaging., • Act as the marketing voice within cross-functional planning and client targeting., • Collaborate on RFP responses and client-specific materials, if needed., • Participate in establishing practices, templates, policies, tools and partnerships to expand and mature these capabilities for the organization., • Develop and deliver progress reports, proposals, requirements documentation and presentations to various audiences, including project team, BD Director, sponsors, and other key stakeholders., • Deliver appropriate and effective executive level communication., • Continue professional development in order to keep abreast of emerging technologies, methods and best practices., • Support in Business Plans. REQUIREMENTS: • Bachelor's Degree in Marketing, Communications, Life Sciences or equivalent work experience., • MBA or master’s in marketing, Life Sciences, or Business is a plus., • 5+ years of marketing experience for complex services. At least 2 years in CDMO, pharma, or biotech industry., • 5+ years of experience working with business stakeholders within a cross-functional matrix environment., • 3+ years of previous experience with Market research and analysis, Digital Marketing (SEO, social media, content marketing, etc), and Data-Driven Decisions to measure ROI and performance., • Technical skills are also desirable. It will be highly desirable Industry-Specific Knowledge and deep understanding of the pharmaceutical value chain, regulatory environment (e.g., FDA, EMA), and B2B marketing dynamics in a CDMO setting. Ability to grasp and communicate technical aspects of drug development, manufacturing, and analytical services., • High English level to understand complex technical and business discussions (written and spoken), communicate fluently and effectively in professional settings. Write clear, well-structured messages, communications, and emails. Present ideas for marketing activities and adapt the communication style for different audiences (scientific, commercial, regulatory)., • Intermediate level of proficiency with CRMs (PipeDrive, Salesforce, etc), MS Project, Excel, Visio, PowerPoint and SharePoint with experience presenting to stakeholders and / or Senior Leadership., • Proven ability to demonstrate a drive for results and accountability of business needs., • Proven ability to work in an ambiguous environment and collaborate across multiple areas in order to achieve a common business objective., • Interpersonal skills to influence and spur change, facilitate and enhance performance within a cross - functional environment., • Demonstrate decisiveness in resolving business problems, making decisions and identifying priorities.

About Us: Zitro is a leading company in the global gaming industry, renowned for its commitment to research, development, and technological innovation. Since its founding in 2007, Zitro has experiences continuous growth, driven by a talented and passionate team. Do you possess the skills and drive to join our success story? Curious to know more about Zitro? Head over to our website: Your day at Zitro: If you're looking for a creative and dynamic environment where you can constantly learn and grow, Zitro is the place for you! As a Copywriter, you'll be a key member of our marketing team, crafting compelling content across all channels: product descriptions, press releases, social media content, articles, and more. In addition to your creative skills, your ability to work as part of a team is equally important. You will work hand-in-hand with other departments, providing an opportunity to learn, grow alongside a talented team, and contribute to the brand’s growth. Key responsibilities: • Create product marketing materials such as game catalogues, promo video scripts, etc..., • Support our Community Manager in crafting engaging social media content., • Write and edit content for quarterly newsletters and email campaigns., • Edit and publish press releases., • Write and translate social content in both English and Spanish., • Conduct competitor analysis., • Bilingual fluency in English and Spanish (written and spoken)., • A minimum of 1 - 3 years of experience in marketing communication or copywriting (experience in communication agencies is a plus)., • Proven ability to balance creative ideas with brand strategy and product content., • Strong writing and content creation skills., • Familiarity with social media scheduling tools., • Team player with excellent communication skills., • A deep passion for writing., • Fantastic work environment and guaranteed fun at Zitro’s regular events, • Permanent contract that will provide stability and confidence in your professional career, • Flexible hours from Monday to Thursday, • Continuous working day on Fridays, • Summer working hours (July and August), • Meal voucher, • Health and life insurance, • Flexible compensation (daycare vouchers)

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

• Liderar la apertura de un nuevo concepto de ocio y entretenimiento Se trata de una organización internacional líder en el sector de hospitalidad y entretenimiento. Actualmente, está en proceso de expansión para establecer una nueva sede en Madrid que fusionará tecnología, ocio y gastronomía premium en un entorno social innovador. Job Description • Actuar como el principal enlace entre las operaciones locales y la sede global., • Supervisar la hoja de ruta de preapertura, que incluye revisiones de diseño, conceptualización de oferta gastronómica y de bebidas, reclutamiento de personal, desarrollo de procedimientos operativos y planificación general., • Construir y liderar un equipo de alto rendimiento, reclutando a los jefes de departamentos clave e impulsando una cultura colaborativa., • Colaborar estrechamente con arquitectos, diseñadores y especialistas en eventos durante la fase de construcción y equipamiento del local., • Desarrollar y gestionar presupuestos operativos, estados financieros (P&L) y CAPEX, asegurando disciplina financiera sin sacrificar la calidad de la experiencia del cliente., • Garantizar que todos los puntos de contacto estén alineados con la visión creativa y los estándares de la marca., • Proveer actualizaciones periódicas del proyecto a los stakeholders internos y externos., • Más de 10 años de experiencia en liderazgo dentro del sector de hospitalidad, entretenimiento o locales de ocio (idealmente con experiencia en simulación, tecnología o experiencias premium)., • Historial comprobado de liderazgo en preaperturas o lanzamiento de nuevos locales o proyectos, preferiblemente en entornos dinámicos y de alta exigencia., • Sólidas habilidades en gestión financiera, con experiencia en P&L, presupuestos y reportes., • Conocimiento profundo del mercado español y europeo será valorado., • Fluidez en inglés; el español es imprescindible. Otros idiomas serán un plus., • Líder nato, con enfoque práctico y capacidad para trabajar bajo presión en ambientes dinámicos y creativos., • Formar parte de un proyecto innovador y en rápido crecimiento, respaldado por una marca globalmente reconocida., • Oportunidad de liderar un equipo apasionado y creativo en un entorno que combina tecnología, ocio y gastronomía premium. #J-18808-Ljbffr