• Ensuring compliance with current Good Manufacturing Practices (GMP) regulations from the receipt of materials to the delivery of the finished product, guaranteeing high-quality, safe, and effective products by efficiently utilizing all available company resources.• Monitoring the processes before INVIMA (Colombia) for new products and modifications to the sanitary registrations of manufactured products.• Keeping the production factory updated in accordance with resolutions and decrees issued by the competent authorities to ensure organizational compliance.• Issuing supporting documents required by internationals commercial partners (Bolivia, Peru, Costa Rica, Ecuador, El Salvador, Nicaragua) to carry out procedures in front of regulatory entities.

• Representative to technology supervision. (Resolution 4816/2008).• Ensure that the stored medical devices and reagents are in the established conditions, with the corresponding documentation and records.• Responsible for maintaining the branch’s CCAA qualifications• Ensure that permanent staff training is carried out and that it is adapted to needs.• Approve the operating procedures related to the storage, conditioning, dispatch and distribution of medical devices and reagents and verify the registration of each process.• Ensure the maintenance and calibration of storage and/or conditioning areas and general facilities.• Monitor and control health records, by adding references or new products.• Ensure that proper process checks and calibrations of control equipment and instruments are carried out, and that these checks are recorded and corresponding reports are available. • Other functions specified in Resolution 4002/2007 and Resolution 132/2006.• Responsible for implementing Quality Systems and Process (ISO).

• Interacting with clinical and non-clinical stakeholders such as: HCP, KOL, proctors, nurses, staff, auditors, purchase and all other key personnel of hospitals and clinics• Providing education on all aspects of the device, device handling, implantation and troubleshooting techniques related to equipment, tools and products required for device implants (Laser systems, ESU, Laparoscopy systems).• Developing and continuously improving training curriculum, training materials and training tools, based on clinical trial experience, SOP guidelines.• Showing business Intelligence.• Throughout commercial procedures, providing physicians and medical staff with required follow-up support to ensure continuity of education and technical support related to all aspects of patient outcome. • Validating software and hardware updates in the field as applicable.• Learning the product(s), physiology, anatomy, applications of the market• Regularly reviewing clinical support activities, changes in the market and assigned accounts, as well as competitive activity with the appropriate Sales Specialist. B2C• Coordinating proctorship assistance if needed and all logistics related.• Monthly expense reporting with no delays.• Other incidental duties.

• Document review of imported devices• Review and maintenance of medical devices sold.

• Hourly wage, in the area of ​​Biomedical Engineering.• Teach the classes assigned to the students.• Plan and develop thematic content of the subjects awarded.• Attend curricular meetings and deliver the relevant documents for the subjects awarded.• Support the functions inherent to the quality management system.

• Scheduling and coordination of teams BMET for review of proactive and vigilance activities according to schedule.• Track execution of CAPA plans according to requirements.• Reception and audit of suppliers.• Creation and monitoring of documentation related to biomedical equipment, planning and execution of maintenance schedules CAPA.• Periodic audits of the resumes of biomedical teams.• Training and medical education of HCP related to biomedical devices in the institution.

To teach in the Maintaince and Merchandising of Biomedical Equipment Program

• Scheduling and coordination of teams BMET for review of proactive and vigilance activities according to schedule.• Track execution of CAPA plans according to requirements.• Training and medical education of HCP related to biomedical devices in the institution.

• Accompaniment in OR (Orthopedics and traumatology, neurosurgery, hand surgery, general surgery, oral maxillofacial surgery, plastic and reconstructive surgery, urological surgery, chest surgery, ophthalmological surgery) in relation to the specialized medical teams of CLINICA UNIVERSIDAD DE LA SABANA• Training and medical education of HCP related to biomedical devices in the institution.• Scheduling and coordination of teams BMET for review of proactive and vigilance activities according to schedule.• Track execution of CAPA plans according to requirements.• Training and medical education of HCP related to biomedical devices in the institution.

Realizar mantenimiento preventivo y mantenimiento correctivo a los equipos médicos del Hospital San Rafael de Facatativá (UCI adultos, Urgencias, UCI neonatal, Odontología, Fisioterapia, Oftalmología, Pediatría, Alto Riesgo Obstétrico, Banco de sangre, Sala de Partos y Salas de Cirugía) y sus Centros de Salud (Odontología, consulta externa, urgencias).Realizar diseño, adecuación, mejoras y repotenciación de dispositivos médicos.

Technical support in database management

Tecnoparque es una red del SENA que busca la innovación tecnológica por parte de emprendedores mediante el préstamo de herramientas, infraestructura y asesoría por parte de expertos.Dentro de la línea de electrónica se desarrolló un proyecto para la implementación del proyecto planteado para mi tesis de grado sobre HMI