Role Description Actualmente nos encontramos en búsqueda del mejor talento para incorporarse al puesto de Cadista. - Recepcionar los dibujos de los proyectistas a través de la plataforma de la empresa. - Elaborar y dibujar los planos de los proyectos asignados mediante AutoCAD, cumpliendo con las normativas vigentes y las especificaciones del cliente. - Entregar los planos terminados a los proyectistas mediante la plataforma de la empresa. - Subsanar las observaciones detectadas por los proyectistas, de ser el caso. - Otras funciones asignadas por su jefe inmediato. Qualifications - Secundaria completa y/o Técnico egresado. - 6 meses a 1 año de experiencia en proyectos de ingeniería ejecutando trabajos en AutoCAD en el rubro electricidad (Baja Tensión/Media Tensión). Benefits - Planilla completa con todos los beneficios de ley. - Salario acorde al mercado. - Beneficios corporativos en los rubros de Educación, Salud y Entretenimiento. - Modalidad de trabajo remoto, con asistencia presencial ocasional a oficina previa coordinación. Company Description Somos Applus+, una de las empresas líderes reconocido en el mercado en el sector de inspección, ensayos y certificación, que ayuda a sus clientes a potenciar la calidad y la seguridad de sus activos, infraestructuras y operaciones, así como su desempeño medioambiental. Nuestra capacidad técnica, de innovación, y nuestro equipo humano altamente cualificado nos permiten asegurar la excelencia operacional en sectores muy diversos en más de 65 países.

At ioet, a leading software company with a talented team across LATAM, we provide Software Engineering as a service to clients worldwide. Join us for exciting professional challenges, working on projects ranging from innovative startups to globally recognized brands. Our positions are full-time, remote, and offer competitive compensation in USD. We are looking for a Software Engineer with strong technical foundations and proven experience in customer-facing technical support. This role sits at the intersection of support, backend investigation, and cloud operations. You will work closely with senior engineers and cross-functional teams to support partner-facing issues, troubleshoot technical problems, and learn how modern systems operate at scale. Responsibilities: - Support partner-facing tickets, prioritizing and resolving issues related to shipments, configurations, APIs, and system errors (P1–P3). - Assist in troubleshooting backend and cloud issues by reviewing logs, running API requests, and analyzing code. - Help monitor AWS-based workflows (SQS, SNS, Lambda) and support operational tasks using tools like CloudWatch - Execute and update scripts and configurations using Python and Git, with support from the team - Collaborate with Engineering, Carrier Operations, and Customer Success teams to resolve issues and improve processes - Document solutions, contribute to internal knowledge bases, and maintain clear communication with partners. Requirements: - 1 year in software development, software engineering, or closely related work - 1 year in customer-facing roles related to technical support - Interest in using AI tools (e.g., Claude, Gemini) to assist with learning, debugging, and code understanding - Hands-on experience with AWS or other cloud platforms in an operational capacity - Experience with ticket management systems such as Jira or similar is a plus - Familiarity with observability tools such as CloudWatch, Datadog, or Elastic is a plus - Strong English communication skills - Minimum B2 level proficiency, C1 preferred - Send your application and CV in English (mandatory) - Based in Latin America Benefits: - Remote work - Flexible schedule - Collaboration with international clients - USD compensation - Paid Holidays and Vacations - Paid family and sick leaves - English classes - Educational and wellness bonus - Structured career plan with regular salary reviews - Emphasis on personal growth and mentorship Are you ready to be part of the ioet journey? Get your CV in English and Apply Now. If you are curious to know more about our culture, technologies, and blogs, visit www.ioet.com

Company Information At Advarra, we are passionate about making a difference in the world of clinical research and advancing human health. With a rich history rooted in ethical review services combined with innovative technology solutions and deep industry expertise, we are at the forefront of industry change. A market leader and pioneer, Advarra breaks the silos that impede clinical research, aligning patients, sites, sponsors, and CROs in a connected ecosystem to accelerate trials. Company Culture Our employees are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives. At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each employee is not only valued but empowered to thrive and make a meaningful impact. Job Overview Summary Advarra has as its core function the institutional review board (IRB) review of a broad spectrum of research ranging from survey research to first-in-human research and sponsored by pharmaceutical companies, biotech companies, institutions, hospitals as well as clinics and private physician offices. The regulatory group is responsible for the expedited review of research, the full board review of research and the documentation of the meeting minutes. The regulatory group also collaborates with other parts of the organization on thought leadership, client guidance and operational efficiencies. At Advarra, the Chairperson leads discussion at full board meetings and ensures that reviews are completed in accordance with Advarra policy and appropriate regulations. This position works with the Chair Director, Senior Chair Director(s), and the Institutional Official (IO) to ensure that Advarra effectively fulfills its obligation to help protect human research subjects. Job Duties & Responsibilities - Maintain superior level knowledge of regulatory requirements, Advarra’s board standard operating procedures, and organizational policies. - Act as a point of contact for Advarra operations staff, assisting with day-to-day challenges - Chair one or more weekly meetings. - Complete expedited reviews for minimal risk research, continuing reviews, investigational brochure updates, and prompt reporting events. - Respond to protocol and informed consent questions for minimal risk or full board protocols. - Ensure appropriate triaging of submissions for minimal risk or full board review. - Review amendments for scientific and non-scientific requirements. - Oversee pre-review of protocols. - Identify areas for guidance and inconsistencies in Board reviews. - Participate in clinically and regulatory-oriented teleconferences. - Consult with sponsors, investigators, and CROs on clinical and regulatory affairs. - Attain and maintain necessary regulatory knowledge for medical device reviews. - Work with Chair Director(s) to identify membership needs and develop board members. - Assist in the annual evaluation of board members. - Onboard and train new unaffiliated board members. - Perform co-chair duties during chairperson onboarding. - Foster a work atmosphere focused on accountability, motivation, team building, training, mentoring, collaboration, and respect. - Identify qualified resources for the board to ensure adequate review expertise. Location This role is open to candidates working remotely in Canada. Basic Qualifications - Bachelor’s degree in a related field. - 1+ years of service chairing IRB meetings or similar experience; 3+ years of experience with an institutional IRB or research experience with a healthcare or clinical research entity within the last 6 years. - Advanced knowledge of all regulations and guidance pertinent to human subject protection in the United States and Canada including, but not limited to AAHRPP, FDA, OHRP, and ICH. - Moderate computer skills including experience with MS Office products. - Certified IRB Professional (CIP) certification within 2 years of employment. Preferred Qualifications - Graduate degree (MS, MA, MD, PhD, DO, etc) - Advanced knowledge of all regulations and guidance pertinent to human subject protection in the United States and Canada including, but not limited to AAHRPP, FDA, OHRP, and ICH. - Moderate computer skills including experience with MS Office products. - Certified IRB Professional (CIP) certification within 2 years of employment. Physical and Mental Requirements - Sit or stand for extended periods of time at stationary workstation. - Regularly carry, raise, and lower objects of up to 10 Lbs. - Learn and comprehend basic instructions. - Focus and attention to tasks and responsibilities. - Verbal communication; listening and understanding, responding, and speaking. Advarra is an equal opportunity employer that is committed to diversity, equity and inclusion and providing a workplace that is free from discrimination and harassment of any kind based on race, color, religion, creed, sex (including pregnancy, childbirth, and related medical conditions, sexual orientation, and gender identity), national origin, age, disability or genetic information or any other status or characteristic protected by federal, state, or local law. Advarra provides equal employment opportunity to all individuals regardless of these protected characteristics. Further, Advarra takes affirmative action to ensure that applicants and employees are treated without regard to any of these protected characteristics in all terms and conditions of employment, including, but not limited to, hiring, training, promotion, discipline, compensation, benefits, and separation from employment. Pay Transparency Statement The base salary range for this role is $125,000 - $160,000 CAD. Note that salary may vary based on location, skills, and experience and may vary from the amounts listed above. This position may also be eligible for a variable bonus in addition to base salary as well as health coverage, paid holidays, and other benefits.

Role Description We are seeking skilled, board-certified Otolaryngologists (ENT) / Head & Neck Surgeons to perform Independent Medical Examinations (IMEs) throughout California. This is an excellent opportunity to earn supplemental income on a contract (1099) basis while maintaining a flexible schedule based on your availability. - Review Medical Records: Analyze patient records related to ear, nose, throat, and head & neck conditions or injuries - Conduct Physical Examinations: Perform in-person ENT evaluations - Address Clinical Questions: Provide objective medical opinions and respond to case-specific questions from insurance carriers - Prepare Reports: Complete clear, comprehensive IME reports within a 5-day turnaround time Qualifications - Board Certification: Must be board-certified in Otolaryngology (ENT) - Experience: Prior IME experience preferred, but not required - Skills: Strong analytical ability, attention to detail, and excellent written and verbal communication skills Benefits - High Volume: Strong and consistent case volume across California - Flexible Scheduling: Accept cases based on your availability - Competitive Compensation: Attractive fee schedule - Organized Documentation: All medical records provided in advance - In-Person Exams: Majority of evaluations conducted face-to-face Company Description