Join to apply for the clinical regulatory lead role at bsi. clinical regulatory lead - active devices location: home based in uk, spain, germany, ireland, netherlands, italy, france bsi is unable to provide relocation or visa sponsorship for this vacancy. due to internal progression, we are looking for a clinical regulatory lead with a specialization in active medical devices to join our global regulatory compliance team. this role will focus on clinical regulatory support to operational teams and internal clinicians of bsi, requiring in-depth experience and knowledge of regulatory requirements for active medical devices. responsibilities include monitoring competence throughout the clinical oversight process via internal auditing. key duties: deliver and support audits of medical devices to maintain awareness of bsi’s systems and handle escalated queries. provide leadership and mentoring in medical device expertise for existing and new global schemes. advise and support global heads, product specialists, and scheme managers. assist the broader team and training lead in developing and delivering internal and external training materials on medical devices, ensuring knowledge of regulatory changes and amendments is current. requirements: strong experience and knowledge of regulatory and compliance requirements of active medical devices. good understanding of medical devices regulations, guidance, and standards. understanding of clinical evaluation processes, data analysis, and clinical study design. about bsi: bsi helps 80,000 clients worldwide improve their businesses, from ...
Join to apply for the clinical regulatory lead role at bsi. clinical regulatory lead - active devices location: home based in uk, spain, germany, ireland, netherlands, italy, france bsi is unable to provide relocation or visa sponsorship for this vacancy. due to internal progression, we are looking for a clinical regulatory lead with a specialization in active medical devices to join our global regulatory compliance team . this role will focus on clinical regulatory support to operational teams and internal clinicians of bsi, requiring in-depth experience and knowledge of regulatory requirements for active medical devices. responsibilities include monitoring competence throughout the clinical oversight process via internal audits. key responsibilities include: deliver and support audits of medical devices to maintain awareness of bsi’s systems and handle escalated queries. provide medical device expertise, leadership, and mentoring for existing and new global schemes. advise and support global heads, product specialists, and scheme managers. assist the broader team and training lead in developing and delivering internal and external training materials on medical devices, ensuring compliance with current regulations and amendments. requirements include: strong experience and knowledge of regulatory and compliance requirements of active medical devices. good understanding of medical devices regulations, guidance, and standards. understanding of clinical evaluation processes, data analysis, and clinical study design. bsi helps 80,000 clients worldwide improve their businesses,...
Join to apply for the clinical regulatory lead role at bsi. clinical regulatory lead - active devices location: home based in uk, spain, germany, ireland, netherlands, italy, france bsi is unable to provide relocation or visa sponsorship for this vacancy. due to internal progression, we are looking for a clinical regulatory lead with a specialization in active medical devices to join our global regulatory compliance team. this role will focus on clinical regulatory support to operational teams and internal clinicians of bsi, requiring in-depth experience and knowledge of regulatory requirements for active medical devices. responsibilities include monitoring competence throughout the clinical oversight process via internal auditing. key duties: 1. deliver and support audits of medical devices to maintain awareness of bsi’s systems and handle escalated queries. 2. provide leadership and mentoring in medical device expertise for existing and new global schemes. 3. advise and support global heads, product specialists, and scheme managers. 4. assist the broader team and training lead in developing and delivering internal and external training materials on medical devices, ensuring knowledge of regulatory changes and amendments is current. requirements: - strong experience and knowledge of regulatory and compliance requirements of active medical devices. - good understanding of medical devices regulations, guidance, and standards. - understanding of clinical evaluation processes, data analysis, and clinical study design. about bsi: bsi helps 80,000 clients worldwide imp...
Join to apply for the clinical regulatory lead role at bsi. clinical regulatory lead - active devices location: home based in uk, spain, germany, ireland, netherlands, italy, france bsi is unable to provide relocation or visa sponsorship for this vacancy. due to internal progression, we are looking for a clinical regulatory lead with a specialization in active medical devices to join our global regulatory compliance team. this role will focus on clinical regulatory support to operational teams and internal clinicians of bsi, requiring in-depth experience and knowledge of regulatory requirements for active medical devices. responsibilities include monitoring competence throughout the clinical oversight process via internal audits. key responsibilities include: 1. deliver and support audits of medical devices to maintain awareness of bsi’s systems and handle escalated queries. 2. provide medical device expertise, leadership, and mentoring for existing and new global schemes. 3. advise and support global heads, product specialists, and scheme managers. 4. assist the broader team and training lead in developing and delivering internal and external training materials on medical devices, ensuring compliance with current regulations and amendments. requirements include: - strong experience and knowledge of regulatory and compliance requirements of active medical devices. - good understanding of medical devices regulations, guidance, and standards. - understanding of clinical evaluation processes, data analysis, and clinical study design. bsi helps 80,000 clients worldwide...
San sebastián is calling for a skilled and dedicated professional to take on the challenging role of head of community nursing. this is a critical position that requires exceptional leadership and clinical expertise. key responsibilities: - develop and implement community nursing strategies aligned with national health policies and priorities. - lead a team of community nurses to provide high-quality patient care and support. - monitor and evaluate the effectiveness of community nursing services, identifying areas for improvement and implementing changes as needed. - collaborate with other healthcare professionals and organizations to ensure seamless care transitions and optimal patient outcomes. requirements include: - strong leadership and management skills with experience in community nursing. - excellent communication and interpersonal skills with the ability to work effectively with diverse stakeholders. - advanced knowledge of community nursing principles, practices, and regulations. - ability to think critically and strategically, driving innovation and excellence in community nursing practice. what we offer: - a competitive salary range between €40,000 and €60,000 per year, reflecting the local market conditions and cost of living. - the opportunity to work in a dynamic and supportive environment with a team of dedicated professionals. - ongoing training and professional development opportunities to enhance your skills and expertise. - a comprehensive benefits package including annual leave, bank holidays, and flexible benefits tailored to your lifestyle. we ...
Clinical regulatory lead role this is a mid-senior level, full-time position within our global regulatory compliance team. key responsibilities: 1. deliver and support audits of medical devices to maintain awareness of bsi's systems and handle escalated queries. 2. provide leadership and mentoring in medical device expertise for existing and new global schemes. 3. advise and support global heads, product specialists, and scheme managers. 4. assist the broader team and training lead in developing and delivering internal and external training materials on medical devices, ensuring knowledge of regulatory changes and amendments is current. requirements: - strong experience and knowledge of regulatory and compliance requirements of active medical devices. - good understanding of medical devices regulations, guidance, and standards. - understanding of clinical evaluation processes, data analysis, and clinical study design....
Requerimos mensajeros motorizados para trabajar en la ciudad de bogotá y alrededores. debe tener conocimiento y experiência en todas las zonas de bogotá y poblaciones aledañas, con experiência comprobable de un año en adelante, manejando mensajería administrativa masiva y/o entrega de facturación de vanti (gas natural). se requiere personal con buena ubicación y orientación en bogotá y municipios aledaños. estudios: bachiller graduado. requisitos personales: excelente manejo de clientes, persona proactiva, dinámica, tolerante a las adversidades y a los cambios bruscos de clima, acostumbrada al trabajo duro, buen manejo del estrés, buen servicio al cliente, paciente y de buen genio. buen manejo del celular. salario: $1. 000 + aux. de transporte + bono de rodamiento y productividad requisitos del vehiculo: moto matriculada en el año 2. 019 en adelante, licencia de conducción vigente, no debe tener comparendos, buenas condiciones de mantenimiento del vehículo, casco no abatible certificado, debe tener coderas, rodilleras, guantes de motorizado y facilidad para instalar baúl. se realiza inspección el día de la entrevista. por favor abstenerse de aplicar a la vacante, si no cumple con algún requisito....
¡Únete a nuestra operación en galapa, colombia! somos un líder en el desarrollo y comercialización de films de polipropileno, poliéster y poliamida. nuestra ubicación estratégica nos permite mantener la velocidad y eficiencia en los requisitos del mercado actual. nuestro objetivo es contar con el mejor talento para nuestra operación. buscamos al coordinador de cogeneración para planificar, organizar y dirigir las actividades operativas y técnicas del proceso de cogeneración de energía eléctrica, garantizando la eficiencia, confiabilidad, continuidad y seguridad de las operaciones. también se buscará liderar al equipo técnico y operativo, asegurando su capacitación adecuada, el cumplimiento de las normas de seguridad y el desempeño eficiente de sus funciones. el responsable velará por el control y monitoreo de la calidad del proceso de generación, asegurando el cumplimiento de los estándares establecidos. responsabilidades clave liderar al equipo técnico y operativo. capacitar adecuadamente al equipo. mantener el cumplimiento de las normas de seguridad. asegurar el desempeño eficiente de las funciones. experiencia y habilidades planificar y organizar actividades operativas y técnicas. dirección de equipos técnicos y operativos. capacitación y desarrollo profesional. mantenimiento de normas de seguridad. requisitos título académico relacionado con la área. experiencia laboral en gestión de proyectos y equipos. habilidad para trabajar en equipo y liderar a otros. conocimiento de procesos de cogeneración de energía eléctrica....
Queremos que hagas parte de nuestro equipo de trabajo: auxiliar de enfermería administrativa, con excelente actitud para atención de pacientes vía telefónica, programación de agendas, asignación de citas y ayudas diagnosticas, realización de contactos telefónicos con pacientes para garantizar el acceso al servicio. horario de 8 horas 6:00 am a 2:00 pm o 2:00 pm a 10:00 pm se requiere buen manejo de excel y word. tipo de puesto: tiempo completo. lugar de trabajo: medellín. tipo de puesto: tiempo completo salario: $1.200.000 - $1.500.000 al mes tipo de puesto: tiempo completo salario: $1.200.000 - $1.500.000 al mes...
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