Maestro de Audicion y Lenguaje - alfa - Córdoba

🛰️ Indra Space – Leading the Next Generation of Space Systems 🌌 At Indra Space, we are on a mission to redefine the European space industry by delivering high-performance small satellite solutions for LEO missions. Our ambition? To become a leading company in end-to-end satellite systems, driving innovation in: 🚀 Position, Navigation & Timing (PNT) 🚀 Secure Communications🚀 Earth Observation & ISR 🚀 Space Domain Awareness (SDA) and Space Traffic Management (STM) 🚀 Science & space exploration As the Space Business Unit of Indra Group, we combine cutting-edge technology with a full value chain approach—from satellite design and integration to ground segment and operations. With the integration of Deimos and strategic participation in Hispasat and Hisdesat, we are scaling Europe’s space autonomy and contributing to flagship programs like IRIS², Galileo, EGNOS, and Copernicus. 🔍 What We’re Looking For We are looking for a System Engineer with solid experience in systems engineering best practices, particularly during the conception, specification, and design phases. The ideal candidate has a strong understanding of GNSS systems and radiofrequency concepts and is comfortable working with complex technical systems in regulated space and defense environments. 📌 Key Responsibilities • Perform system engineering activities across GNSS-related projects, from concept definition to detailed specification and design.• Manage and track system requirements using tools such as DOORS or similar, and follow up activities using tracking tools like JIRA., • Contribute to the analysis and definition of GNSS system concepts, signals, performances, and interference detection and geolocation., • Analyse radiofrequency aspects including link budgets, RF and baseband subsystems., • Operate and analyse data from RF instrumentation such as spectrum analyzers, oscilloscopes, and power meters., • Apply MBSE approaches using tools such as Capella, Enterprise Architect, or similar., • Produce clear and structured technical documentation in line with project and customer requirements., • Work in compliance with ESA ECSS or similar applicable standards., • Collaborate effectively with multidisciplinary teams, contributing to technical discussions and system-level decisions. 🎯 Requirements • Experience in systems engineering best practices, especially in conception, specification, and design phases.• Experience with requirement management tools such as DOORS (or similar) and tracking tools such as JIRA., • Understanding of GNSS systems, including system concepts, GNSS signals, system performances, RF interference detection, and geolocation., • Solid understanding of radiofrequency concepts, including link budgets and RF/baseband subsystems., • Hands-on experience with RF instrumentation (spectrum analyzers, oscilloscopes, power meters)., • Experience with MBSE management tools such as Capella, Enterprise Architect, or equivalent., • Ability to analyse complex technical systems and produce high-quality technical documentation., • Familiarity with ESA ECSS standards or similar space/defense standards., • Strong communication skills and ability to work effectively within technical teams., • Fluent English with strong verbal and written communication skills. What We Offer: 🌍 Work Your Way: Flexible hours so you can balance life and work effortlessly. 🤝 Open Culture: Direct communication and a friendly environment where your voice matters. 🚀 Innovation at Its Core: Be part of groundbreaking projects with global impact. 💡 People First: A collaborative team that supports and celebrates your success. 📈 Career Acceleration: Continuous feedback and annual reviews to help you grow. 🔒 Stability You Can Trust: Long-term projects in a leading company with a future vision. 🌐 Global Reach: Your work will influence major international initiatives. ✈️ Mobility Opportunities: Explore projects across Spain and beyond. 🎓 Lifelong Learning: Access Open University programs and 3,000+ Udemy for Business courses. Your next big opportunity is here. Ready to make an impact? Apply today! Our commitment is to promote work environments where people are treated with respect and dignity, fostering the professional development of our workforce and guaranteeing equal opportunities in recruitment, training and promotion. We provide a workplace free from any form of discrimination based on gender, age, disability, sexual orientation, gender identity or expression, religion, ethnicity, marital status, or any other personal or social circumstance. INDRA is a Top Employer 2026! Join a company certified as one of the best employers in Spain, thanks to our comprehensive HR management and the working conditions we offer our professionals.

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.

Role Overview We are currently inviting qualified ESL teachers to apply for a remote instructional role supporting international learners through our structured online teaching platform. This is a contract-based teaching position offering self-managed scheduling within a professional global education environment. Why Join Us • Remote teaching structure, • Self-managed scheduling, • Access to professional development opportunities, • Supportive global educator network, • Dedicated online teaching portal Core Requirements · Bachelor’s Degree or higher · Recognized English teaching certification (TESOL / TEFL / TESL – CELTA or equivalent preferred) · Minimum of 2 years ESL teaching experience · Demonstrated commitment to professional growth and teaching excellence Professional Qualifications (Preferred) · Advanced ESL qualifications (Level 5 equivalent or higher such as CELTA, TKT, DipTESOL, PGCE, MEd, PhDEd) · Continuous professional development (CPD) participation · Experience with international learners Language Capability Requirements · English proficiency at CEFR C2 (or equivalent) is required · Proficiency in at least one additional language at CEFR B1+ or higher is strongly preferred Teaching Scope You may support either young learners or adult learners depending on teaching allocation. Students may include: • School-aged learners, • University students, • Working professionals, • Adult learners seeking conversational fluency All curriculum materials are provided and accessible in advance of teaching sessions. Next Step • Qualified candidates are invited to submit their resume for review.

It's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Bring your strengths and let us grow together. We are hiring a Clinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) Your Strength • Minimum of 4 years of advanced experience in clinical research monitoring, • In-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.g., ISO 14155, GCP, MDR, EU, FDA), • Ability to independently manage 10–15 study sites from start-up through close-out, • Excellent communication skills for site interaction, training, and issue resolution, • Strong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members, • Hands-on experience with monitoring systems, source data verification, and compliance tracking, • Strong organizational skills with the ability to manage multiple priorities in a dynamic environment, • Willingness to travel regularly for site visits and investigator meetings across France and Spain, • Based in Spain (candidates from France may be considered in case a candidate lives nearby the Spain/France border and eager to do cross border monitoring), • Fluent communication in English and Spanish (Catalan is preferred, French optional) Your Contribution • Independently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out, • Conduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements, • Act as the primary contact for investigational sites, ensuring compliance and providing ongoing support, • Build and maintain strong relationships with investigators, study coordinators, and site personnel, • Identify study risks, recommend solutions, and ensure timely resolution of site-related issues, • Perform source data verification and data review to ensure patient safety, protocol compliance, and data integrity, • Conduct site training, initiation visits, and support audit and inspection readiness, • Collaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams, • Support investigator meetings, coordinator meetings, and deliver presentations or training sessions when required, • Mentor junior CRAs and contribute to process improvements and best practices, • Participate in CAPA activities, quality initiatives, audits, and continuous improvement efforts Our Strength • A mission-driven company focused on saving lives, • International and collaborative MedTech environment, • Hybrid working model with flexibility, • Opportunities for growth and professional development, • Innovative products and meaningful clinical impact Contact Apply now and join the Artivion team. We look forward to receiving your application documents in English through our online application system. Brian Russo T: +41 435 08 39 01 JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc. Lotzenäcker 23, 72379 Hechingen www.artivion.com

Researcher Training is a client-facing function that imparts training to researchers, universities, and corporate clients through live in-person sessions and online webinars. We have a global pool of trainers who conduct these events for our research base around the world. Training topics include manuscript writing, journal selection, submission package, grant writing, science communication, graphical abstracts, case report writing, thesis writing, AI for research, etc. The training session formats: • In-person workshops (CACTUS will cover travel and other domestic expenses), • Online webinars As an Academic Publication Trainer and Consultant, you will work closely with the training team and be involved in delivering high-quality training programs to researchers from various disciplines which may on occasions include reviewing manuscripts of researchers and offering on-site, one-on-one guidance for how to improve them further. Some requests also include preparing training materials, while others could involve live sessions on a social channel. Essential duties and responsibilities • Delivering high-quality training., • Preparing and customizing training content as per request., • Understanding in adequate detail the author services Editage, CACTUS offers., • Collaborate with the training team on designing the outline of training programs on the basis of client requirements, modifying training content and approach on the basis of feedback shared by Editage or the client., • Occasionally reviewing research manuscripts written by workshop participants either before or during sessions and sharing personalized feedback and tips with participants on how to improve the language, flow, structure, and other aspects of content presentation. Knowledge and skills: • PhD in the field of Physical Sciences., • Excellent oral and written communication skills in Spanish(Native)., • Experience in publishing research articles in international high-impact-factor journals., • In-depth knowledge of processes and trends in the academic publishing industry., • High level of ownership and ability to work with tight deadlines.

Open Longevity is an independent research organization focused on aging, regeneration, and life extension. Our work includes the Open Genes database, peer-reviewed publications, research roadmaps, books, and collaborative research projects. We are looking for a biologist who can turn scientific ideas and preliminary results into strong grant applications. Most of your work will involve developing proposals together with experimental and computational research groups: shaping the central hypothesis, writing the scientific narrative, defining aims and milestones, and coordinating the preparation of preliminary data. You will also help keep bioinformatics and experimental work aligned with the needs of upcoming applications. As the projects develop, you will have opportunities to participate in research papers and scientific reviews arising from this work. We are looking for someone who has • A PhD in biology, neuroscience, regenerative medicine, aging research, or a related field., • Substantial experience contributing to at least one successfully funded grant application., • Excellent scientific writing skills in English., • Experience working with experimental or computational research groups., • The ability to move a project from an initial discussion to a clear, submission-ready proposal. Experience with US or European grant applications is a strong advantage. We are particularly interested in scientists who want to take greater ownership of research programs and grow toward scientific leadership. This is a fully remote position intended as a stable, long-term collaboration. Compensation will be discussed individually based on experience and the scope of the role. • To apply, please send your CV and a brief description of one or two grant applications you contributed to, including what you personally did.

Open Longevity is an independent research organization focused on aging, regeneration, and life extension. Our work includes the Open Genes database, peer-reviewed publications, research roadmaps, books, and collaborative research projects. We are looking for a biologist who can turn scientific ideas and preliminary results into strong grant applications. Most of your work will involve developing proposals together with experimental and computational research groups: shaping the central hypothesis, writing the scientific narrative, defining aims and milestones, and coordinating the preparation of preliminary data. You will also help keep bioinformatics and experimental work aligned with the needs of upcoming applications. As the projects develop, you will have opportunities to participate in research papers and scientific reviews arising from this work. We are looking for someone who has • A PhD in biology, neuroscience, regenerative medicine, aging research, or a related field., • Substantial experience contributing to at least one successfully funded grant application., • Excellent scientific writing skills in English., • Experience working with experimental or computational research groups., • The ability to move a project from an initial discussion to a clear, submission-ready proposal. Experience with US or European grant applications is a strong advantage. We are particularly interested in scientists who want to take greater ownership of research programs and grow toward scientific leadership. This is a fully remote position intended as a stable, long-term collaboration. Compensation will be discussed individually based on experience and the scope of the role. • To apply, please send your CV and a brief description of one or two grant applications you contributed to, including what you personally did.

Clinical Research and Regulatory Specialist | MedTech Location: Spain (Remote) Employment type: Full-time Role Summary We are looking for a motivated junior professional who wants to develop their career in the MedTech and IVD sector. As a Clinical Research and Regulatory Specialist, you will support clinical research activities, scientific and medical writing, and the creation of documentation essential to product validation and regulatory pathways. You will work closely with senior experts and multidisciplinary teams, gaining hands-on experience with clinical investigations, performance studies (ISO 14155 and ISO 20916), technical documentation, and clinical evidence development. Ideal for candidates with 0.5–2 years of experience in MedTech, IVD, clinical research or R&D — or strong scientific backgrounds eager to enter the industry. Responsibilities You will: • Support the preparation and execution of Clinical Investigations and Performance Studies, • Assist in developing study documentation (protocols, CRFs, ICFs), • Collaborate with study sites and internal teams following ISO 14155 and ISO 20916 standards, • Handle study documentation and communication with investigators, • Assist with monitoring‑support activities and data‑related tasks, • Contribute to scientific and medical writing, including study summaries and evidence-based content, • Support literature reviews, background research, and documentation preparation, • Assist in drafting components of clinical evidence documentation under supervision, • Help coordinate project activities, timelines, and communication You will receive structured onboarding, mentoring, and progressive responsibility. You are not expected to know everything on day one — you will learn with us. Requirements (Must‑Have) • Based in Spain or eligible for a Spanish employment contract, • 0.5–2 years of experience in MedTech, IVD, clinical research, or R&D, • Strong interest in MedTech, IVDs, clinical research, and scientific development, • Bachelor’s degree in Life Sciences, • Enrolment in or completion of a Master’s degree in Life Sciences, • Knowledge of GCP and clinical/lab standards, • Advanced English (C1–C2), especially for scientific writing, • Motivation to grow in a dynamic and international environment, • Availability for remote work with occasional in‑person activities Nice to Have • Exposure to ISO 14155 or ISO 20916, • R&D experience, • Regulatory exposure, • Academic research experience or authorship in scientific literature Why Join MDx CRO At MDx CRO, you will join a dynamic and rapidly growing company recognised across the MedTech and IVD industry. We offer: • Structured onboarding and continuous training, • Close mentorship from senior specialists, • Exposure to real clinical and scientific projects, • Growth opportunities as your skills develop About MDx CRO MDx CRO is a leading Contract Research Organisation specialising in in vitro diagnostics (IVDs) and medical devices. We provide regulatory consulting, clinical research, and quality assurance services, helping clients bring safe and effective products to market in full compliance with global regulatory standards. We operate on five core principles: • Make it POSSIBLE, • Make it WIN-WIN, • Keep IMPROVING, • Keep GROWING, • Keep it DIVERSE Our Vision To democratise access to world-class regulatory and clinical strategies, ensuring safer and more effective medical technologies for all. Our Mission We pioneer emerging technologies and navigate uncharted territories to redefine the future of the medical sector. Grow with Us If you want to accelerate your development in the MedTech and IVD sector within a supportive and expert‑driven environment, we would love to hear from you.