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• Academia Centro de Estudios Actual

  

  Profesor/a de Ciencias

  hace 9 horas

  €10 por hora

  Jornada parcial

  Carretera de Cádiz, Málaga

  Profesor/a de Matemáticas y Química – Academia en Málaga Ubicación: Calle Conejito de Málaga, Málaga capital Jornada: Parcial, 7 horas semanales Horario: Martes y jueves, de 17:30 a 21:00 h Salario: 10 € netos/hora Incorporación: Inmediata Descripción del puesto Academia de apoyo escolar situada en Calle Conejito de Málaga (Málaga) busca estudiante universitario/a de Química, Ingeniería Química o carrera científica similar para impartir clases de Matemáticas y Química a alumnos de ESO y Bachillerato, hasta 2.º de Bachillerato. Buscamos una persona responsable, paciente, cercana con los alumnos y con facilidad para explicar. Requisitos • Estar cursando o haber cursado estudios universitarios de Ciencias o Ingeniería., • Buen dominio de Matemáticas y Química hasta 2.º de Bachillerato., • Capacidad para explicar de forma clara y adaptarse a distintos niveles., • Disponibilidad los martes y jueves por la tarde., • No es necesaria experiencia docente previa. ¿Qué ofrecemos? • Contrato laboral y alta en la Seguridad Social., • Remuneración de 10 € netos por hora., • Horario fijo, compatible con estudios universitarios., • Ambiente de trabajo cercano., • Incorporación inmediata. ¡Si te gustan las ciencias y disfrutas ayudando a los alumnos a aprender, nos encantará conocerte!

  ¡Incorporación inmediata!

  Sin experiencia

  Inscripción fácil
• Savia, Aprendizaje Creativo

  

  Profesor/a Particular de Matemáticas, Física y Química

  hace 1 mes

  €200–€300 mensual

  Jornada parcial

  Málaga-Este, Málaga

  Dos tardes a la semana, presencial, para alumnos/as de 4 eso y primero y segundo de bachillerato.

  ¡Incorporación inmediata!

  Sin experiencia

  Inscripción fácil
• English Academy

  

  Profesor/a de inglés dinámico/a – Niños y adolescentes

  hace 2 meses

  Jornada parcial

  Málaga

  Buscamos profesores/as dinámicos/as y creativos/as, a quienes les apasione trabajar con niños y adolescentes y que entiendan la enseñanza como una combinación de aprendizaje, participación y diversión. Queremos una persona resolutiva, expresiva, responsable y comprometida con nuestra filosofía de enseñanza, con ganas de involucrarse activamente en las clases y formar parte de nuestro equipo. Requisitos: • Nivel mínimo B2 de inglés, tanto oral como escrito., • Experiencia trabajando con niños., • Capacidad para desarrollar clases dinámicas y participativas. Valoramos especialmente la experiencia impartiendo inglés a niños y adolescentes.

  Inscripción fácil
• Tusclasesparticulares

  

  Teletrabajo - Profesor/a Particular - Sin Experiencia

  hace 5 meses

  Málaga

  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.

• EF Education First

  

  Activity Leader - málaga

  hace 5 días

  Málaga

  Overview In this role you will lead activities, events, and excursions for international students, ensuring days are engaging, safe, and memorable. You will create welcoming atmospheres, manage group dynamics, and deliver high-quality experiences across city tours, themed events, and games. You will supervise safety, conduct risk assessments, and handle emergencies following EF policies. You will collaborate with the Activity Manager on planning and support content for EF social channels. Responsabilidades • Provide students with information and assistance regarding activities and excursions, • Create a lively, welcoming atmosphere during events and trips, delivering exceptional service, • Support community management and help maintain a vibrant environment within the school, • Ensure health, safety, and well-being of all students, including conducting risk assessments and managing emergencies in line with EF policies, • Lead guided tours at excursion destinations, sharing engaging content (materials provided by EF), • Accompany students to attractions and ensure smooth logistics throughout the trip, • Safeguard under-18 students during all activities in accordance with EF guidelines, • Assist with event promotion, including creating and displaying posters, • Prepare detailed handovers for the Activity Manager to ensure seamless service, • Report any emergencies promptly to the manager, • Attend activity meetings and implement action points as required, • Support content creation for EF social media channels Requisitos principales, • Highly motivated, energetic, and positive with sociable, outgoing personality, • Confident in leading and managing groups of students, • Organised, proactive, and able to work independently, • Calm under pressure and skilled at handling challenging situations, • Customer-focused and committed to delivering quality experiences, • Culturally aware and respectful of diversity, • Excellent communication skills with students, colleagues, and external partners, • Flexible with working hours and tasks, including availability for evening and weekend activities, • Fluent in Spanish and English, • sociable, • outgoing, • calm under pressure, • risk assessments, • logistics coordination, • content creation for EF social media channels

• Thermo Fisher Scientific

  

  Senior Clinical Research Associate I (FSP) - Thermo Fisher Scientific

  hace 4 días

  Málaga

  This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Summarized Purpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or supervising environments (i.e. FSO, FSP, Government, etc.). Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability. Ensures audit readiness. Develops collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to role are outlined in the task matrix. Location Information This is a home-based position and preferably based in Western/Southern Australia Key responsibilities Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts supervising tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable. Participates in investigator meetings as vital. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials. Ensures that required crucial documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications. Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System). Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts. Responds to company, client and applicable regulatory requirements/audits/inspections. Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner. Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Contributes to other project work and initiatives for process improvement, as required. Keys to Success Education and Experience: Bachelor's degree in a life sciences related fielder a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor) Knowledge, Skills and Abilities: Proven clinical monitoring skills. Demonstrated understanding of medical/therapeutic area knowledge and medical terminology Demonstrated ability to attain and maintain a solid understanding of ICH GCPs, applicable regulations and procedural documents. Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving Ability to manage Risk Based Monitoring concepts and processes. Good oral and written communication skills, with the ability to communicate effectively with medical personnel. Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues. Good organizational and time management skills Effective interpersonal skills. Attention to detail. Ability to remain flexible and adaptable in a wide range of scenarios. Ability to work in a team or independently as required. Good digital literacy: solid knowledge of Microsoft Office and the ability to learn appropriate software. Good English language and grammar skills. Good presentation skills. Australian citizenship or permanent residency required Benefits Join our team and take advantage of these great benefits! Apply now to learn more about the full range of benefits we offer. Health & Wellbeing: Join a company that prioritizes your health & wellbeing with comprehensive benefits, wellness programs, and an Employee Assistance Program providing confidential support for personal and work-related issues. Flexibility: Balance your work and personal life with flexible arrangements. Extra Leave: Benefit from generous leave policies, including the option to purchase additional leave, paid birthday leave, and company paid parental leave. Charitable Giving & Volunteering: Make an impact with paid volunteer time to support non-profit organizations that matter to you. Learning & Development: Advance your career with access to online courses via Thermo Fisher Scientific University Plus and LinkedIn learning, workshops, and mentorship programs for continuous learning and skill development. Thermo Fisher Scientific Australia WGEA Employer of Choice for Gender Equality We offer competitive remuneration, annual incentive plan bonus, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

• EF Education First

  

  Activity Leader

  hace 5 días

  Málaga

  Overview In this role you will lead activities, events, and excursions for international students, ensuring days are engaging, safe, and memorable. You will create welcoming atmospheres, manage group dynamics, and deliver high-quality experiences across city tours, themed events, and games. You will supervise safety, conduct risk assessments, and handle emergencies following EF policies. You will collaborate with the Activity Manager on planning and support content for EF social channels. Responsabilidades • Provide students with information and assistance regarding activities and excursions, • Create a lively, welcoming atmosphere during events and trips, delivering exceptional service, • Support community management and help maintain a vibrant environment within the school, • Ensure health, safety, and well-being of all students, including conducting risk assessments and managing emergencies in line with EF policies, • Lead guided tours at excursion destinations, sharing engaging content (materials provided by EF), • Accompany students to attractions and ensure smooth logistics throughout the trip, • Safeguard under-18 students during all activities in accordance with EF guidelines, • Assist with event promotion, including creating and displaying posters, • Prepare detailed handovers for the Activity Manager to ensure seamless service, • Report any emergencies promptly to the manager, • Attend activity meetings and implement action points as required, • Support content creation for EF social media channels Requisitos principales, • Highly motivated, energetic, and positive with sociable, outgoing personality, • Confident in leading and managing groups of students, • Organised, proactive, and able to work independently, • Calm under pressure and skilled at handling challenging situations, • Customer-focused and committed to delivering quality experiences, • Culturally aware and respectful of diversity, • Excellent communication skills with students, colleagues, and external partners, • Flexible with working hours and tasks, including availability for evening and weekend activities, • Fluent in Spanish and English, • sociable, • outgoing, • calm under pressure, • risk assessments, • logistics coordination, • content creation for EF social media channels

• Thermo Fisher Scientific

  

  Senior Clinical Research Associate I (FSP) - málaga

  hace 4 días

  Málaga

  This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Summarized Purpose: Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or supervising environments (i.e. FSO, FSP, Government, etc.). Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability. Ensures audit readiness. Develops collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to role are outlined in the task matrix. Location Information This is a home-based position and preferably based in Western/Southern Australia Key responsibilities Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts supervising tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable. Participates in investigator meetings as vital. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials. Ensures that required crucial documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications. Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System). Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts. Responds to company, client and applicable regulatory requirements/audits/inspections. Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner. Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Contributes to other project work and initiatives for process improvement, as required. Keys to Success Education and Experience: Bachelor's degree in a life sciences related fielder a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor) Knowledge, Skills and Abilities: Proven clinical monitoring skills. Demonstrated understanding of medical/therapeutic area knowledge and medical terminology Demonstrated ability to attain and maintain a solid understanding of ICH GCPs, applicable regulations and procedural documents. Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving Ability to manage Risk Based Monitoring concepts and processes. Good oral and written communication skills, with the ability to communicate effectively with medical personnel. Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues. Good organizational and time management skills Effective interpersonal skills. Attention to detail. Ability to remain flexible and adaptable in a wide range of scenarios. Ability to work in a team or independently as required. Good digital literacy: solid knowledge of Microsoft Office and the ability to learn appropriate software. Good English language and grammar skills. Good presentation skills. Australian citizenship or permanent residency required Benefits Join our team and take advantage of these great benefits! Apply now to learn more about the full range of benefits we offer. Health & Wellbeing: Join a company that prioritizes your health & wellbeing with comprehensive benefits, wellness programs, and an Employee Assistance Program providing confidential support for personal and work-related issues. Flexibility: Balance your work and personal life with flexible arrangements. Extra Leave: Benefit from generous leave policies, including the option to purchase additional leave, paid birthday leave, and company paid parental leave. Charitable Giving & Volunteering: Make an impact with paid volunteer time to support non-profit organizations that matter to you. Learning & Development: Advance your career with access to online courses via Thermo Fisher Scientific University Plus and LinkedIn learning, workshops, and mentorship programs for continuous learning and skill development. Thermo Fisher Scientific Australia WGEA Employer of Choice for Gender Equality We offer competitive remuneration, annual incentive plan bonus, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!