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📢We are looking for a results-driven, enthusiastic and proactive Upstream Technician to join our Manufacturing Operations Department. 🚀 Main Responsibilities: As a USP Manufacturing Technician, your responsibilities will include: • Ensure the timely compliance with the planning of the USP Scale-Up and Manufacturing department previously made by a Team leader., • Ensure the correct training of the personnel in charge., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Participate in internal / external audits as required by the Quality Assurance Department., • Comply and ensure compliance with GMP standards within the work team., • Record and manage any quality indicators associated with a scale-up and manufacturing process. Participate in the investigation of the same together with the Team Leader USP (FAB)., • Investigate and propose new methods or process innovations to optimize and improve the work in the area., • Ensure proper compliance with regulations and correct completion of current documentation., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and their manager., • Perform the entry documentation of new equipment from the USP Scale-up and Manufacturing area under the supervision of the Team Leader USP (FAB)., • Supervise the correct completion of the new equipment entry documentation., • Supervise the correct training of the personnel in charge, if any., • Carry out the distribution and supervision of daily activities., • Write and keep updated the documentation associated with the production processes carried out in the USP area., • Control / monitoring of orders placed in the USP production area using ERP software. 📚 Assesment criteria: Education: Bachelor's degree in Pharmacy; Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, cell culture etc . Desirable but not required Master's degree or equivalent in related fields. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • With bioreactors, • Cell Cultures, • Microbiological analysis techniques, • Upstream production positions, • Biotechnology / Biopharmaceutical Sector Other requirements: • Open to work in shifts., • Software package: Office. User level. 💊Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

📢Career Development Opportunity📢 Are you looking for an opportunity to develop your professional career in a CDMO Manufacturing Operations Department? From day one on, 3PBIOVIAN has been inspired from the people that conforms it, and because of that matter, one of the main values of the company has always been the professional and personal growth of its employees in an international and biotechnological environment. Due to this prioritization, Navarra site of 3PBIOVIAN is currently looking for professionals who want to focus their careers in Scale Up and Manufacturing department USP and DSP both. As 3PBIOVIAN is committed to the continuous, updated and personalized improvement of our personnel´s learning, our Learning and Development department is focused in offering opportunities for professional growth and opting for an environment of trust. The successful candidate will join 3PBIOVIAN, in Navarra, Spain, as part of our Scale Up and Manufacturing department. The candidate will be expected to provide strategic development oversight know-how and technical input in specific tasks and in the group in general. In addition, the candidate will be involved in the manufacturing to obtain products (biomass or recombinant proteins) with the specifications required by our clients, in the execution of the tech transfer processes; as well as contribution to routine laboratory activities. 🚀 What we´re looking for: • Experience in either Manufacturing departments in upstream and/or downstream processes, in the biotechnological industry., • People who have performed manufacturing activities in either the Upstream processing or Downstream processing area according to GMP guidelines, ensuring batch execution, evaluating test results, resolving issues and make proposals for resolution., • People who assists document preparation (e.g electronic batch records, SOPs) specific to the assigned manufacturing area., • Experience in working with bioreactor and filtration systems is desirable., • Experience in a GMP environment., • Proven initiative and independent thinking to deliver tasks on time, whilst working in a team environment., • A person capable to identify technical and scientific problems and discuss possible solutions., • Fluency in Spanish, fluency in English is considered a plus., • Open to work in shifts. 💊What we offer: • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • And so much more! 💥 Do you want to know us better? 🌟It´s within us.

La Clínica Universidad de Navarra busca incorporar un/a investigador con formación en biología, bioquímica, farmacia o inmunología para su participación en un proyecto internacional. Esta posición está orientada a personas con vocación investigadora, y entusiasmo por el desarrollo tecnológico en el ámbito sanitario. Funciones principales: • Recepción de muestras externas y pre-procesado (sangre, orina, tejido renal)., • Estudio de micro-disección laser en glomérulos en colaboración con laboratorio de histología., • Estudio de proteómica y transcriptómica en colaboración con laboratorio de histología., • Colaboración con el equipo médico en la identificación y reclutamiento de pacientes a nivel local en CUN., • Colaboración con el equipo médico en la identificación de posibles candidatos a nivel nacional. Requisitos: • Master o doctor en biología, bioquímica, farmacia o inmunología., • Experiencia en investigación. Se ofrece: • Incorporación inmediata., • Contrato temporal., • Jornada completa., • Entorno de trabajo colaborativo, con acceso a tecnología puntera., • Somos una empresa responsable en materia de conciliación familiar y laboral, ofrecemos otros beneficios sociales de carácter personal y familiar, añadidos a la retribución salarial. Este proyecto recibió financiación del Gobierno de Navarra en el marco de la Asociación Europea para la Medicina Personalizada, EP PerMed (GA nº 101137129 del Programa de Investigación e Innovación Horizonte Europa de la UE).

📢We are looking for a goal-oriented, proactive, and motivated Downstream Technician to join our Manufacturing Operations Department. 🚀 Main Responsibilities: As a DSP Manufacturing Technician, your responsibilities will include: • Achieve the objectives set by the Team Leader and the DSP manufacturing manager., • Prepare, control and develop processes for the production of recombinant proteins, monoclonal antibodies or similar biological molecules in microorganisms., • Comply with good manufacturing practice (GMP), as well as occupational health and safety standards., • Maintain equipment and facilities in perfect state of repair, ensuring that they are operated according to the manuals provided by the manufacturer., • Conduct and/or supervise chromatographic runs, as well as all other manufacturing operations., • Ensure that the necessary material orders are scheduled in the SAP system to meet the production schedule according to the project and the weekly production plan., • Carry out the control and supervision, the stock of materials needed to perform the daily activities., • Prepare, pack, evaluate and unpack chromatography columns, as well as supervise these operations performed by Operators., • Program chromatography methods in UNICORN to ensure the correct execution of DSP processes., • Prepare and ensure the correct preparation of solutions required for the performance of manufacturing activities., • Participate in internal / external audits as required by the Quality Assurance Department., • Participate in the correct transfer of technologies and resources between companies related to 3P Biopharmaceuticals in collaboration with other departments and your manager. Documentary responsibilities: • Perform the incoming documentation of new equipment from the Scaling and Manufacturing DSP area under the supervision of the Team Leader DSP (FAB)., • Ensure the maintenance of up to date technical documentation of the DSP process, as well as all documentation related to assigned tasks., • Record and manage any quality indicators associated with a scaling and manufacturing process. Participate in the investigation of the same together with the Team Leader DSP (FAB)., • Oversee and write SOPs that correspond to the activities carried out in the Scaling and Manufacturing DSP department., • Prepare the documentation related to the quality system associated with the DSP Scale-up and Manufacturing plant: Deviations; Change Controls; Action Plans; Corrective, preventive and improvement actions, etc.). 📚 Assesment criteria: Education: • Advanced Vocational Training or equivalent in related areas (Biology, Biochemistry, Biotechnology, Chemistry, Health, Clinical Laboratory, etc.)., • University Degree or equivalent in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA; Chemical Engineering, etc.)., • Master's Degree in related areas (Biology; Biochemistry; Biotechnology; Chemistry; IPPA, etc.) is valued but not required. Languages: Fluent in Spanish. Intermediate level of English (Level B2 / First Certificate). Between 1 and 2 years of experience in/with: • GMP/GLP regulations, • Chromatographic equipment, • Packed chromatographic columns, • Experience with ÄKTA, • Experience with Unicorn Other requirements: • Open to work in shifts., • Office Software Package: User Level., • Unicorn Software Package: User Level. 💊Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • Company benefits club, which allows 3PBIOVIAN employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • 3PBio is committed to the continuous, updated and personalized improvement of our personnel's learning. To this end, we have Learning & Development department, who is in charge of creating personalized, individualized and differentiating career plans for our employees., • The company continues to focus on internal talent and stable employment, focusing on upskilling and reskilling. We offer opportunities for professional growth and take an environment of trust., • We encourage the participation of our employees in solidarity events such as charity races, social donations..., • We have several programs aimed at improving the physical, psychological and emotional well-being of our employees. In this context, we participate in the Corporate Challenge, promote healthy lunches and comfortable and safe work spaces., • We have a high-impact work environment with flat hierarchies and short decision-making processes., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and GMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human and animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

📢 We are looking for a results-driven, dynamic, and self-motivated Quality Control Supervisor Technician to join our Physicochemical Laboratory. 🚀Main responsibilities: As a Quality Control Supervisor Technician, your responsibilities will include: • Ensure GMP activities in the physicochemical laboratory., • Evaluate and review the technical documentation corresponding to the Quality Control of the physicochemical laboratory, as well as the analytical results in routine manufacturing, validation and transfer activities., • Organize and ensure compliance with the weekly program and coordinate human, material and technical resources to ensure its achievement., • Propose process improvements aimed at improving quality, cost, performance, time and safety of workers and the environment., • To train and qualify the analysts to carry out the controls correctly., • Maintain the installations in perfect state of conservation ensuring that they are operated according to the manuals provided by the manufacturer., • Carry out the drafting and supervision of standard operating procedures (SOP's)., • Carry out the resolution of deviations in the laboratory., • Coordinate the release of raw materials and the analysis of intermediates, drug substances and drug products., • Support stability studies agreed with our customers in collaboration with other technicians., • Provide production quality support in case of incidents that may arise., • Approve and close CAPAS (corrective and preventive actions) arising from deviations and applicable efficacy verification., • Check the correct traceability of the materials consumed in the analysis process. 📚 Assesment criteria: Education: • University Degree or equivalent in Chemistry; Biotechnology; Biology or similar., • Master's degree related to the area of study., • PhD in a related area is valued, but not necessary Languages: • Fluent in Spanish. Intermediate level of English (B1 level / First Certificate) At least 4 years of work experience in/with: • Use of techniques such as HPLC, UV and IR Spectrophotometry, UPLC, Fluorescence, DAD, UV-VIS…, • Experience with recombinant proteins, mAbs, Biosimilar, ADCs (desirable)., • Experience with pharmaceutical regulatory guidelines., • Use of Agilent equipment with Empower 3 software. Other requirements: • Open to work in shifts. 💊 Why 3PBiovian? • A permanent and stable position in a competitive growing company., • A competitive time off package with 41 paid days of vacation., • Flexible compensation plan, allowing all employees to allocate up to 30% of their gross annual salary to daily services exempt from income taxes (childcare, health insurance, academic training etc.), • Company benefits club, which allows 3P Biovian employees to obtain exclusive prices and discounts on a multitude of products and services (Booking, FNAC, Rituals, El Corte Inglés etc.), • All new hires who reside outside Navarra are provided with a relocation service and/or assistance., • ...And so much more! 💥Why us? We know it takes people with passion and a shared purpose to manufacture advanced medicines. We specialize in process development and cGMP manufacturing of biologics and cell therapy products using microbial and mammalian expression systems. We are with you on your biologics journey, growing with you and supporting you with process and analytical development, preclinical and clinical supply, and commercial production. With a focus on biotechnology applications in both human an animal health sectors, we offer customized solutions that meet the specific needs of all our clients From development to product delivery, we are with you on your biologics journey. We are a leading global CDMO and preferred partner for pharmaceutical and biotech companies. We have what it takes to help you improve lives. 🌟It's within us.

SE BUSCA UN DOCTOR/A EN MICROBIOLOGÍA CON EXPERIENCIA DE AL MENOS 5 AÑOS GESTIONADO PROYECTOS, PERSONAS Y/O SERVICIOS. • CONOCIMIENTOS AMPLIOS EN MICROBIOLOGÍA: LEVADURAS, BACTERIAS Y HONGOS., • GESTION DE PERSONAS, • EXPERIENCIA EN BIOLOGÍA MOLECULAR Y CLONAJE., • EXPERIENCIA EN UPSTREAM Y DOWNSTREAM., • SE ENCRGARA DE DESARROLLAR Y EJECUTAR PROYECTOS DE I+D Y SERVICIOS DE LA EMPRESA, • PERSONA CON INICIATIVA, DINIMICA, ENTUSIASTA, DETALLISTA, RIGUROSA Y CONSTANTE. Beneficios sociales: • Teléfono móvil Especialidad: • Microbiología, Biología Molecular, Upstream/Downstream

Se busca profesores/estudiantes/universitarios para brindar clases de distintas materias a estudiantes de diferentes niveles educativos (primaria, secundaria, bachillerato o universidad). No se requiere experiencia previa como profesor.

La Clínica Universidad de Navarra busca incorporar un/a investigador con formación en biología, bioquímica, farmacia o inmunología para su participación en un proyecto internacional.Esta posición está orientada a personas con vocación investigadora, y entusiasmo por el desarrollo tecnológi

🇺🇸 Clinical Research Associate (CRA) – USA Relocation Opportunity CROVELIS is currently looking for experienced Clinical Research Associates (CRAs) interested in relocating to the United States for a long-term international clinical research assignment. This position offers the opportunity to join a global clinical operations team supporting high-impact international studies in a fast-paced and highly collaborative environment. Selected candidates will relocate to the US for an estimated period of 2–3 years, with relocation and visa support provided by the company. 📍 Location: United States ✈️ Visa & relocation support included 🕒 Long-term assignment (2–3 years) 🔎 What are we looking for? • Minimum 4 years of experience as a CRA in clinical trial monitoring, • Strong experience performing:, • • Site Selection Visits (SSV), • • Site Initiation Visits (SIV), • • Routine Monitoring Visits (RMV), • • Close-Out Visits (COV), • Solid understanding of ICH-GCP, FDA regulations, and clinical operations processes, • Experience managing investigative sites independently and ensuring protocol compliance, • Ability to work in dynamic, fast-paced, and international environments, • Strong communication, organizational, and stakeholder management skills, • Previous exposure to multicountry/global clinical trials is highly valued, • Fluent English level required 💼 Key Responsibilities As a CRA, you will play a critical role in the successful execution of international clinical trials across multiple sites in the United States. Responsibilities will include: • Overseeing site performance and ensuring studies are conducted according to protocol, GCP, SOPs, and regulatory requirements, • Conducting site qualification, initiation, routine monitoring, and close-out visits, • Building strong relationships with investigators, coordinators, and site staff, • Ensuring patient safety, data integrity, and overall study quality throughout the trial lifecycle, • Reviewing source documentation, identifying protocol deviations, and supporting issue resolution, • Collaborating closely with Clinical Trial Managers, vendors, sponsors, and cross-functional teams, • Supporting site activation, enrollment, and retention strategies, • Maintaining accurate and timely study documentation and monitoring reports, • Participating in investigator meetings, trainings, and study planning activities 🚀 Why join CROVELIS? CROVELIS is building a globally focused internal CRO designed to deliver high-quality clinical trial execution through agility, collaboration, and innovation. This role offers a unique opportunity to combine: ✅ International relocation to the US ✅ Career growth within global clinical operations ✅ Exposure to complex and high-visibility studies ✅ Multicultural and collaborative environment ✅ Long-term international experience If you are looking to take your CRA career to an international level and be part of a growing global organization, we would love to hear from you.

🇺🇸 Clinical Research Associate (CRA) – USA Relocation Opportunity CROVELIS is currently looking for experienced Clinical Research Associates (CRAs) interested in relocating to the United States for a long-term international clinical research assignment. This position offers the opportunity to join a global clinical operations team supporting high-impact international studies in a fast-paced and highly collaborative environment. Selected candidates will relocate to the US for an estimated period of 2–3 years, with relocation and visa support provided by the company. 📍 Location: United States ✈️ Visa & relocation support included 🕒 Long-term assignment (2–3 years) 🔎 What are we looking for? • Minimum 4 years of experience as a CRA in clinical trial monitoring, • Strong experience performing:, • • Site Selection Visits (SSV), • • Site Initiation Visits (SIV), • • Routine Monitoring Visits (RMV), • • Close-Out Visits (COV), • Solid understanding of ICH-GCP, FDA regulations, and clinical operations processes, • Experience managing investigative sites independently and ensuring protocol compliance, • Ability to work in dynamic, fast-paced, and international environments, • Strong communication, organizational, and stakeholder management skills, • Previous exposure to multicountry/global clinical trials is highly valued, • Fluent English level required 💼 Key Responsibilities As a CRA, you will play a critical role in the successful execution of international clinical trials across multiple sites in the United States. Responsibilities will include: • Overseeing site performance and ensuring studies are conducted according to protocol, GCP, SOPs, and regulatory requirements, • Conducting site qualification, initiation, routine monitoring, and close-out visits, • Building strong relationships with investigators, coordinators, and site staff, • Ensuring patient safety, data integrity, and overall study quality throughout the trial lifecycle, • Reviewing source documentation, identifying protocol deviations, and supporting issue resolution, • Collaborating closely with Clinical Trial Managers, vendors, sponsors, and cross-functional teams, • Supporting site activation, enrollment, and retention strategies, • Maintaining accurate and timely study documentation and monitoring reports, • Participating in investigator meetings, trainings, and study planning activities 🚀 Why join CROVELIS? CROVELIS is building a globally focused internal CRO designed to deliver high-quality clinical trial execution through agility, collaboration, and innovation. This role offers a unique opportunity to combine: ✅ International relocation to the US ✅ Career growth within global clinical operations ✅ Exposure to complex and high-visibility studies ✅ Multicultural and collaborative environment ✅ Long-term international experience If you are looking to take your CRA career to an international level and be part of a growing global organization, we would love to hear from you.

🇺🇸 Clinical Research Associate (CRA) – USA Relocation Opportunity CROVELIS is currently looking for experienced Clinical Research Associates (CRAs) interested in relocating to the United States for a long-term international clinical research assignment. This position offers the opportunity to join a global clinical operations team supporting high-impact international studies in a fast-paced and highly collaborative environment. Selected candidates will relocate to the US for an estimated period of 2–3 years, with relocation and visa support provided by the company. 📍 Location: United States ✈️ Visa & relocation support included 🕒 Long-term assignment (2–3 years) 🔎 What are we looking for? • Minimum 4 years of experience as a CRA in clinical trial monitoring, • Strong experience performing:, • • Site Selection Visits (SSV), • • Site Initiation Visits (SIV), • • Routine Monitoring Visits (RMV), • • Close-Out Visits (COV), • Solid understanding of ICH-GCP, FDA regulations, and clinical operations processes, • Experience managing investigative sites independently and ensuring protocol compliance, • Ability to work in dynamic, fast-paced, and international environments, • Strong communication, organizational, and stakeholder management skills, • Previous exposure to multicountry/global clinical trials is highly valued, • Fluent English level required 💼 Key Responsibilities As a CRA, you will play a critical role in the successful execution of international clinical trials across multiple sites in the United States. Responsibilities will include: • Overseeing site performance and ensuring studies are conducted according to protocol, GCP, SOPs, and regulatory requirements, • Conducting site qualification, initiation, routine monitoring, and close-out visits, • Building strong relationships with investigators, coordinators, and site staff, • Ensuring patient safety, data integrity, and overall study quality throughout the trial lifecycle, • Reviewing source documentation, identifying protocol deviations, and supporting issue resolution, • Collaborating closely with Clinical Trial Managers, vendors, sponsors, and cross-functional teams, • Supporting site activation, enrollment, and retention strategies, • Maintaining accurate and timely study documentation and monitoring reports, • Participating in investigator meetings, trainings, and study planning activities 🚀 Why join CROVELIS? CROVELIS is building a globally focused internal CRO designed to deliver high-quality clinical trial execution through agility, collaboration, and innovation. This role offers a unique opportunity to combine: ✅ International relocation to the US ✅ Career growth within global clinical operations ✅ Exposure to complex and high-visibility studies ✅ Multicultural and collaborative environment ✅ Long-term international experience If you are looking to take your CRA career to an international level and be part of a growing global organization, we would love to hear from you.

Investigador/a Especialista en Ciberseguridad.

Investigador/a Especialista en Ciberseguridad.

Investigador/a Software en Computación Cuántica.

Investigador/a Software en Computación Cuántica.

Investigador/a Teórico en Computación Cuántica.

En Academia BIKAIN buscamos profesor/a de matemáticas, física y química para el curso 2026-27!. Te gustaría formar parte de una academia joven, cercana y comprometida con el aprendizaje y el desarrollo de sus alumnos? En BIKAIN queremos seguir creciendo y ampliar nuestro equipo docente incorpora

Investigador/a Teórico en Computación Cuántica.

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El personal docente deberá acreditar experiencia docente y profesional. Seleccionamos docente para la impartición de. Contrato de colaboración (dependiendo del Régimen de colaboración de la persona Docente: Alta en SS o Autónomo).

El personal docente deberá acreditar experiencia docente y profesional. Seleccionamos docente para la impartición de. Contrato de colaboración (dependiendo del Régimen de colaboración de la persona Docente: Alta en SS o Autónomo).

Buscamos Logopeda o Maestra Especialista en Audición y Lenguaje para nuestro centro de Atención Temprana concertado con la Comunidad de Madrid! Si disfrutas trabajando con peques y quieres formar parte de un amplio equipo interdisciplinar referente en Atención Temprana con más de 15 años de exp

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En el marco de su crecimiento institucional, UTAMED continúa ampliando su claustro académico con la incorporación de Personal Docente e Investigador (PDI), reforzando especialmente las titulaciones vinculadas al ámbito educativo y la formación del profesorado. UTAMED es una universidad online c

Colaboración con el equipo médico en la identificación y reclutamiento de pacientes a nivel local en CUN. Esta posición está orientada a personas con vocación investigadora, y entusiasmo por el desarrollo tecnológico en el ámbito sanitario. Estudio de micro-disección laser en glomérulos en

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En el marco de su crecimiento institucional, UTAMED continúa ampliando su claustro académico con la incorporación de Personal Docente e Investigador (PDI), reforzando especialmente las titulaciones vinculadas al ámbito educativo y la formación del profesorado. UTAMED es una universidad online c

En el marco de su crecimiento institucional, UTAMED continúa ampliando su claustro académico con la incorporación de Personal Docente e Investigador (PDI), reforzando especialmente las titulaciones vinculadas al ámbito educativo y la formación del profesorado. UTAMED es una universidad online c

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Buscamos incorporar diferentes posiciones con profesores/as contratados doctores, a tiempo completo para impartir diferentes asignaturas (según el área, se valorará formación específica en Psicología General Sanitaria, Metodología de las Ciencias del Compartamiento, Epidemiología, Enfermerí

EOCB0008 – Preparación Básica para Actividades de Mantenimiento General de Infraestructuras en Edificios e Instalaciones.Esta formación está orientada a dotar al alumnado de conocimientos básicos y prácticos para desarrollar tareas de apoyo en mantenimiento general de edificios, instalacione

Buscamos incorporar diferentes posiciones con profesores/as contratados doctores, a tiempo completo para impartir diferentes asignaturas (según el área, se valorará formación específica en Psicología General Sanitaria, Metodología de las Ciencias del Compartamiento, Epidemiología, Enfermerí

Buscamos incorporar diferentes posiciones con profesores/as contratados doctores, a tiempo completo para impartir diferentes asignaturas (según el área, se valorará formación específica en Psicología General Sanitaria, Metodología de las Ciencias del Compartamiento, Epidemiología, Enfermerí

En Academia BIKAIN buscamos profesor/a de matemáticas, física y química para el curso 2026-27!. Te gustaría formar parte de una academia joven, cercana y comprometida con el aprendizaje y el desarrollo de sus alumnos? En BIKAIN queremos seguir creciendo y ampliar nuestro equipo docente incorpora

Investigador/a Especialista en Ciberseguridad.

Investigador/a Teórico en Computación Cuántica.

The primary responsibility of the (Clinical) Oversight Monitor (C)OM) is to ensure adequate Sponsor oversight of the conduct, monitoring and management of one or more clinical studies and assigned monitors at clinical study sites, within the assigned country or region. May conduct oversight monitori

The primary responsibility of the (Clinical) Oversight Monitor (C)OM) is to ensure adequate Sponsor oversight of the conduct, monitoring and management of one or more clinical studies and assigned monitors at clinical study sites, within the assigned country or region. May conduct oversight monitori

Como Educador/a Infantil y/o Maestro de Infantil/Primaria serás responsable de organizar y llevar a cabo actividades educativas diseñadas para fomentar el desarrollo temprano de los niños. Conocimientos en desarrollo infantil temprano y experiencia previa trabajando con niños pequeños. Competen

Como Educador/a Infantil y/o Maestro de Infantil/Primaria serás responsable de organizar y llevar a cabo actividades educativas diseñadas para fomentar el desarrollo temprano de los niños. Conocimientos en desarrollo infantil temprano y experiencia previa trabajando con niños pequeños. Competen

Como Educador/a Infantil y/o Maestro de Infantil/Primaria serás responsable de organizar y llevar a cabo actividades educativas diseñadas para fomentar el desarrollo temprano de los niños. Conocimientos en desarrollo infantil temprano y experiencia previa trabajando con niños pequeños. Competen

May conduct oversight monitoring visits, co-monitoring visits, monitoring visit report reviews and other Sponsor oversight activities per applicable study plans, as needed. The primary responsibility of the (Clinical) Oversight Monitor (C)OM) is to ensure adequate Sponsor oversight of the conduct, m

Profesor/a de Mecánica Motorsport. Desde MSi Racetech Institute buscamos incorporar un/a Profesor/a de Mecánica para impartir formación técnica a alumnos interesados en desarrollarse profesionalmente dentro del sector de la automoción y el motorsport.

EOCB0008 – Preparación Básica para Actividades de Mantenimiento General de Infraestructuras en Edificios e Instalaciones.Esta formación está orientada a dotar al alumnado de conocimientos básicos y prácticos para desarrollar tareas de apoyo en mantenimiento general de edificios, instalacione

Profesor/a de Mecánica Motorsport. Desde MSi Racetech Institute buscamos incorporar un/a Profesor/a de Mecánica para impartir formación técnica a alumnos interesados en desarrollarse profesionalmente dentro del sector de la automoción y el motorsport.

EOCB0008 – Preparación Básica para Actividades de Mantenimiento General de Infraestructuras en Edificios e Instalaciones.Esta formación está orientada a dotar al alumnado de conocimientos básicos y prácticos para desarrollar tareas de apoyo en mantenimiento general de edificios, instalacione

Profesor/a de Mecánica Motorsport. Desde MSi Racetech Institute buscamos incorporar un/a Profesor/a de Mecánica para impartir formación técnica a alumnos interesados en desarrollarse profesionalmente dentro del sector de la automoción y el motorsport.