Game Master Escape Room de Miedo - Creepy Rooms S.L

Similar jobs

• JOSE MARTÍNEZ JACOBE

  

  Game Master

  7 days ago

  €7 hourly

  Part-time

  Sants, Barcelona

  Necesitamos a una persona para trabajar de Game Máster en un escape room. El trabajo es para fines de semana, sábados y domingos, y el horario máximo es de 9:30 a 15:30 El Game Máster ha de ser una persona responsable, extrovertida, que tenga facilidad en el trato con clientes, con unas ciertas dotes para la actuación y que se pueda comunicar fluidamente en Catalán, Castellano, e Inglés.

  Immediate start!

  Easy apply
• Elements Escape Room

  

  Game Master

  1 month ago

  €9 hourly

  Part-time

  Esplugues de Llobregat

  Buscamos a una persona para trabajar de Game Master en Elements Escape rooms Esplugues, con disponibilidad para trabajar fines de semana y valorable disponibilidad entre semana. Las funciones del puesto incluyen: • Recibir a los clientes, • Explicar las normas del juego., • Realizar el seguimiento de la partida., • Despedir al grupo al finalizar la experiencia. Requisitos: • Nivel de inglés Avanzado., • Habilidades de interpretación y canto, • Don de gentes., • Carácter resolutivo y proactivo., • Se valora haber jugado a escape room

  Immediate start!

  No experience

  Easy apply
• Abbott Laboratories

  

  Go Software Engineer - Cloud

  27 days ago

  Barcelona

  About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. Interested in applying your wealth of technical knowledge and experience towards an opportunity in the medical field and improve the lives of people? In our new Technology Hub in Barcelona, you will join our purpose driven team to: • Drive innovation in health tech by developing scalable platforms that transform real-time biosensor data into meaningful insights., • Shape the future of digital health by building solutions that empower people to take control of their metabolic health., • Create engineering with a global impact by working on technology that reaches millions worldwide., • Advance accessibility and compatibility by ensuring our solutions integrate seamlessly across devices and ecosystems. Candidates will work with a modern tech stack on a Software as a Service cloud platform as well as internal and external APIs to improve the health and well-being of users in over 25 countries in a large-scale system responsible for processing billions of messages daily. The candidate should bring passion for software engineering and a desire for continuous learning as well as versatility, leadership qualities and a desire to shape the direction of the team. Candidate will support building scalable, highly available, efficient, and secure cloud solutions for a medical device SaaS. #software Responsibilities • Design and implement services and components utilizing Go for cloud-based platforms., • Collaborate with internal and external partners to develop and integrate with APIs that empower users to share and utilize their medical data in partner systems., • Design and implement unit testable code that are highly maintainable., • Collaborate directly with InfoSec to design and implement secure solutions., • Provide new ideas and insight in collaboration with the data services team., • Ensure performance, uptime, and scale, maintaining high standards of code quality and thoughtful design., • Contribute to significant architectural and operational decisions in collaboration with the Architecture team., • Build out our internal tooling and APIs to make business and engineering processes more efficient., • Implement systemic changes to align existing systems with current architectural goals., • Create diagrams, flowcharts and models that illustrate the internal design and workflow of solution components., • Engage in technical planning, design, and code reviews including peer code reviews., • Collaborate as an enaged member of an agile team, realizing features through development, test, and delivery., • Stay current with emerging trends, making recommendations as needed to help the organization innovate. Required Qualifications • Bachelors Degree in Computer Science, Information Technology or other relevant field., • Software development experience, ideally in Go. A willingness to learn new software development languages to meet goals and objectives., • Strong Computer Science fundamentals and experience with software development., • Understands Object Oriented Programming and design and building modular unit testable code., • Understands the principles of designing, implementing, and maintaining highly complex asynchronous messaging and backend processing jobs., • Understands the concepts of Docker Containers and container orchestration services such as Docker Swarm, ECS, and Kubernetes.., • Experience with Git for source control on a collaborative project., • Comfortable working asynchronously with a distributed team. Preferred Qualifications • Practical experience and understanding of working with and developing RESTful APIs and microservices., • Experience contributing to a scalable architecture/design of existing and new systems that are highly available and easy to maintain and monitor., • Understanding and familiarity of Test Driven Development (TDD)., • Experience working with relational datastores such as SQL Server, Postgresql, or MySql., • Experience working in an agile environment.., • Practical Knowledge of Linux.

• DigiTech Resourcing

  

  Research Scientist – Causal Inference - UpTo €100k - Hybrid

  3 days ago

  Barcelona

  Research Scientist – Causal Inference – Pharmaceutical Applications Barcelona - Hybrid Upto €100k + Benefits (depending on experience) I’m partnering with a cutting-edge pharmaceutical company that is redefining how artificial intelligence is applied to medicine and chemistry. They’re expanding their research team and are looking for a deeply curious, intellectually rigorous Research Scientist – Causal Inference to focus on fundamental research with real-world scientific impact. This is not a pure implementation role. It’s for someone who loves to think critically, challenge assumptions, and develop new ideas from first principles. What You’ll Be Doing: • Developing and improving foundational AI and data-driven research methods., • Applying advanced approaches to complex observational and longitudinal studies in medicine and chemistry., • Collaborating with domain experts to translate abstract scientific ideas into tangible results., • Publishing research in leading international, peer-reviewed journals., • Contributing actively to the academic community (presenting, refereeing, and discussing research). What you need: • Strong research track record with peer-reviewed publications., • Ability to independently develop novel ideas, not just execute existing methods., • Proficiency in Python., • Solid grounding in Machine Learning and Deep Learning fundamentals., • Intellectual honesty, self-awareness, and the ability to manage a full research workload. Highly Desirable: • Background in Mathematics, Physics, Chemistry, or Biology (preferred over traditional CS/AI-only backgrounds)., • Understanding of advanced causal reasoning and related algorithms., • Backend coding experience. Prior causality experience is not essential — the company is looking for exceptional researchers eager to learn and will provide the necessary training.

• ZeClinics

  

  Laboratory Technician

  2 days ago

  Barcelona

  ZeClinics is HIRING a Laboratory Technician! ZeClinics offers an exciting opportunity for a Laboratory Technician to be part of the team, whose mission is to provide an outsourcing solution for safety and efficacy screenings of novel chemical molecules using zebrafish. The ideal candidate would be responsible for performing experiments and support our Facility Manager in the daily organization of ZeClinics´s Laboratory. Duties of the Laboratory Technician will include: • Perform the experimental tasks related to both scientific services offered by the company to third parties and research and development pipelines., • Analyze the data deriving from experimental approaches., • Ensure the correct use of defined laboratory equipment and maintain them up to date., • Support the Project managers in redacting reports for clients (preparing the text and figures)., • Organize the data derived from the experiments and lab books to ensure full traceability of results., • Support quality validation following GLP-like and GLP regulations and drafting SOPs., • Support in regulatory studies if needed. Studies Holding a Bachelor’s or Master’s degree (and equivalent) in biotechnology, biology, biochemistry, biomedical laboratory science, or a related discipline will be necessary. Experience to value • Proven experience with cellular biology, molecular biology, basic pharmacology, high throughput assays, and other biochemical, molecular, or cellular techniques will be mandatory., • Experience with chemicals administration, microinjection, zebrafish biology, and husbandry will be positively evaluated., • FELASA certification to perform scientific experiments with animals will be a plus. Additional skills • Ability to work independently and interact with several collaborators, • Exceptional organizational skills with strict attention to detail, • Ability to manage multiple projects simultaneously under tight deadlines Languages Good command of Spanish is mandatory, knowledge of English both verbal and written, will be greatly appreciated. The Offer • Duration: Indefinite contract, • Trial period: 3 months, • Estimated annual gross salary: ranging from 23.000 to 25.000 euros per year (depending on experience)., • Flexibility is required to work on weekends during peak service periods, with the preference for having two days per week where weekly and weekend schedules can be interchanged. All applications must include: • A presentation letter addressed to Flavia De Santis and Anna Navarro (Project Managers), • A full CV including contact details, • Two contacts for further references All applications must be sent to the HR DEPARTMENT by e-mail to

• Grupo Nortempo

  

  Profesor/a de Catalán

  1 day ago

  Barcelona

  Buscamos incorporar un/a Profesor/a de Catalán para el curso académico 2026-2027 en centro educativo consolidado. 📍 Incorporación: 1 de septiembre de 2026 📄 Contrato: Indefinido 🕘 Jornada completa: 8:45 a 16:45h (algunos días 8:15h) 💰 Retribución bruta anual prevista: 41.655€ 🍽️ Desayuno y comida incluidos 📚 Formación requerida incluida Funciones: • Docencia en ESO (1º a 4º) y Bachillerato (según perfil), • Posibilidad de impartir en 6º de Primaria, • Tutoría de grupo (según perfil) Requisitos: • Mínimo 2 años de experiencia docente en secundaria, • Grado en Filología Catalana o Filología Hispánica + Máster de Formación del Profesorado (ESO y Bachillerato), • Se valorará Grado en Educación Primaria, • Catalán nativo Buscamos un perfil con sólida vocación docente, capacidad de trabajo en equipo y compromiso con el proyecto educativo.

• Leitat Technological Center

  

  QUALITY CONTROL LEAD

  3 days ago

  Barcelona

  ¿Te interesa formar parte de un centro tecnológico de excelencia donde podrás contribuir y añadir valor tecnológico a empresa e instituciones, centrándote en la investigación, el desarrollo y la innovación industrial (I+D+2i)? ¿Quieres trabajar en un entorno puntero con todas las innovaciones tecnológicas a tu alcance? Leitat es un centro tecnológico de referencia a nivel estatal y europeo. Con más de 100 años de historia, cuenta con un equipo de más de 400 profesionales, expertos en investigación aplicada, servicios técnicos y gestión de iniciativas tecnológicas y de innovación. Leitat aporta valor social, industrial, económico y sostenible, ofreciendo soluciones integrales en múltiples sectores y ámbitos: salud y biomedicina, desarrollo de nuevos materiales, producción eco-sostenible, sistemas de prevención de salud laboral, revalorización de residuos y aprovechamiento de recursos naturales; interconectividad y digitalización de la industria, energía verde y maximización de la eficiencia energética. Leitat desarrolla proyectos de I+D+i para empresas e instituciones, así como lidera proyectos de investigación con financiación competitiva tanto en el marco de la Unión Europea como del Ministerio de Ciencia e Innovación Actualmente buscamos un/a Responsable en Control de Calidad, para nuestra sede de Gene Vector, participando activamente en el control analítico y cumplimiento normativo de procesos relacionados con vectores virales. Tus principales funciones serán: Control y análisis de calidad: • Ejecución de análisis de materias primas, controles en proceso (IPC) y producto terminado conforme a protocolos establecidos., • Evaluación de resultados frente a especificaciones y análisis de parámetros críticos de lentivirus., • Realización de ensayos microbiológicos, analíticos y de potencia. Documentación y cumplimiento GMP: • Elaboración de informes de análisis y registro de datos conforme a normativa GMP., • Documentación y gestión de desviaciones, asegurando la trazabilidad completa del muestreo y los análisis., • Redacción, revisión y actualización de procedimientos operativos y protocolos analíticos. Muestreo, equipos y proveedores: • Diseño y ejecución de planes de muestreo., • Gestión de reactivos, materiales de referencia y revisión de Certificados de Análisis (CoA)., • Seguimiento de calibración, mantenimiento y validación de equipos (IQ/OQ/PQ)., • Coordinación con proveedores y comunicación de requisitos de calidad. Análisis de tendencias y mejora continua: • Seguimiento y análisis de tendencias de resultados analíticos., • Identificación y reporte de desviaciones o resultados fuera de especificación a Garantía de Calidad., • Participación en formaciones internas de QC. ¿Qué esperamos de ti? Licenciatura o Grado en Ciencias de la Vida (Medicina, Farmacia, Química, Bioquímica, Biología, Biotecnología, Biomédica o similar). Valorable Máster en Terapias Avanzadas (ATMP) o formación específica en Control de Calidad. Experiencia: Mínimo 2–3 años en Control de Calidad dentro de Industria farmacéutica o biofarmacéutica, producción de medicamentos de terapias avanzadas (ATMP, terapia génica) Conocimientos técnicos: • GMP/NCF, BPL, • Regulación AEMPS/EMA para ATMP, • Guías ICH (Q2, Q3, Q6, Q7, Q9, Q10), • Bioseguridad y manipulación de vectores virales (lentivirus) Idiomas: Castellano e inglés, valorable Catalán. Ofimática: Manejo de software de laboratorio y nivel avanzado de Microsoft Office. Triunfarás en esta posición si eres una persona: • Metódica, constante y orientada al detalle., • Organizada, rigurosa y disciplinada., • Flexible, con capacidad para gestionar urgencias., • Con buenas habilidades de comunicación y trabajo en equipo., • Comprometida con el cumplimiento normativo y la calidad. Se valorará disponer de certificado de discapacidad. ¿Cómo es trabajar en Gene Vector? Estarás ubicado/a en la sede de Barcelona, en un entorno atractivo, siendo parte de un ecosistema de innovación único con tecnologías de vanguardia y laboratorios altamente equipados. Te ofrecemos un contrato indefinido y jornadas de trabajo flexible para que puedas conciliar tu vida personal y tu desarrollo profesional. Además, podrás disfrutar de catering subvencionado en nuestros centros y seguro médico. Estamos orgullosos de ofrecer este tipo de beneficios que apoyan los objetivos y el bienestar de los miembros de nuestros equipos. Asimismo, apoyamos la igualdad de oportunidades y la diversidad. ¡Nos esforzamos cada día por ser un lugar de trabajo más inclusivo adaptado a todos los colectivos! Si eres una persona con excelentes habilidades interpersonales y de comunicación, con una alta capacidad para lograr tus objetivos en los plazos establecidos y capaz de trabajar de manera independiente y en equipo, no lo dudes, inscríbete a nuestra oferta. ¡Nos encantaría saber de ti! ¡En Gene Vector estamos deseando conocerte!

• ARTO

  

  Medical Director Clinical Development

  4 days ago

  Barcelona

  Medical Director, Clinical Development (Global Clinical Lead) Location: Barcelona, Catalonia, Spain ARTO are partnered with a global Pharmaceutical company, who are committed to the growth of their portoflio within the Medical Dermatology space. Role Overview This role provides global medical and scientific leadership for a late-phase clinical development program. The Medical Director (Clinical Lead) will own clinical strategy and execution across Phase II–III studies, acting as the accountable clinical lead within a cross-functional global team and supporting progression toward registration. Key Responsibilities • Provide global medical and scientific leadership for a late-phase (Phase II–III) clinical development program, ensuring delivery against quality, timelines, and strategic objectives., • Define and drive the clinical development strategy, including Target Product Profile (TPP), study concepts, and alignment with regulatory and commercial goals., • Serve as the clinical lead within global, cross-functional project teams, partnering closely with Clinical Operations, Regulatory Affairs, Safety, Biometrics, and Medical Affairs., • Act as the medical accountable lead for late-phase clinical studies, including protocol development, data review and interpretation, and ongoing benefit–risk evaluation., • Represent the clinical program in interactions with external stakeholders, including investigators, key opinion leaders, and regulatory authorities as required. Candidate Profile & Qualifications • MD required, with board certification or equivalent clinical training; Dermatology background a strong plus., • Approximately 5+ years of experience in pharmaceutical or biotechnology clinical development, with exposure to late-phase programs., • Demonstrated experience contributing at program level within Clinical Development, beyond single-study execution., • Solid scientific grounding in immunology-driven diseases (e.g. dermatology, allergy, inflammatory or immune-mediated indications)., • Strong understanding of late-phase trial design, clinical data interpretation, and global regulatory expectations. If you think this role would be a good fit for you, please feel free to reach out to me either through DM, or on email -