Terumo Neuro
Terumo Neuro is a division of Terumo Corporation, a global medical technology company. They specialize in developing and manufacturing innovative medical devices for neurovascular interventions. Their product portfolio includes a range of catheters, guidewires, and other devices designed to treat conditions affecting the brain and spinal cord, aiming to improve patient outcomes and reduce the invasiveness of surgical procedures.
The company is committed to advancing neurovascular care through continuous research and development, collaborating with healthcare professionals to create solutions that meet the evolving needs of the medical field.
37 empleos en Terumo Neuro
Sr. Technician, Supplier Quality - CR
Alajuela
Terumo Neuro
Hoy
Trabajo visto
Descripción Del Trabajo
**13121BR**
**Title:**
Sr. Technician, Supplier Quality - CR
**Job Description:**
This role supports the supplier quality activities related to development and manufacture of medical devices. The position will work with Engineers to address various product reliability and quality issues. This role will be in charge of the execution of the IQOQ process for RI equipment's, execution of TM, execution of inspection routines, control of calibrated equipment and drawing and receiving specification changes in quality system. Job duties:
+ Assists Engineers with investigation of raw material, product and process quality issues.
+ Assists Engineers with product testing and test method validations.
+ Assists Engineers with IQOQ executions.
+ Assists with activities related to equipment calibration, corrective/preventive actions, nonconformance reports, internal audits and CAPA projects.
+ Monitors all activities to ensure the product is processed properly through the entire process from receipt through transfer to finished goods.
+ Performs analysis and identifies trends in the inspection of finished products, in-process materials, raw materials, and recommends corrective actions when necessary.
+ Problem solving and root cause analysis activities with suppliers and customers to eliminate recurrence of defects.
+ Performs additional duties as assigned.
**Auto req ID:**
13121BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3211-CR-Quality
**Qualifications:**
1. High School Diploma or equivalent.
2. Minimum three (3) years of technical work experience in the medical device industry.
3. Strong written and verbal communications. Good interpersonal skills.
4. Advance studies on Industrial engineering or similar career.
5. 70% English required.
**Desired Qualifications**
1. Knowledge of medical product manufacturing and quality.
2. Experience with medical device testing; experience testing MicroVention products is a plus.
3. Ability to read and follow test procedures.
4. Ability to perform product inspections; ability to understand technical documentation including mechanical drawings.
5. Good computer skills especially with Word and Excel.
6. Ability to work in controlled environments (clean rooms).
7. Ability to work under pressure.
8. Teamwork skills.
**External-Facing Title:**
Sr. Technician, Supplier Quality - CR
**Posting Country:**
Outside US
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
**Title:**
Sr. Technician, Supplier Quality - CR
**Job Description:**
This role supports the supplier quality activities related to development and manufacture of medical devices. The position will work with Engineers to address various product reliability and quality issues. This role will be in charge of the execution of the IQOQ process for RI equipment's, execution of TM, execution of inspection routines, control of calibrated equipment and drawing and receiving specification changes in quality system. Job duties:
+ Assists Engineers with investigation of raw material, product and process quality issues.
+ Assists Engineers with product testing and test method validations.
+ Assists Engineers with IQOQ executions.
+ Assists with activities related to equipment calibration, corrective/preventive actions, nonconformance reports, internal audits and CAPA projects.
+ Monitors all activities to ensure the product is processed properly through the entire process from receipt through transfer to finished goods.
+ Performs analysis and identifies trends in the inspection of finished products, in-process materials, raw materials, and recommends corrective actions when necessary.
+ Problem solving and root cause analysis activities with suppliers and customers to eliminate recurrence of defects.
+ Performs additional duties as assigned.
**Auto req ID:**
13121BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3211-CR-Quality
**Qualifications:**
1. High School Diploma or equivalent.
2. Minimum three (3) years of technical work experience in the medical device industry.
3. Strong written and verbal communications. Good interpersonal skills.
4. Advance studies on Industrial engineering or similar career.
5. 70% English required.
**Desired Qualifications**
1. Knowledge of medical product manufacturing and quality.
2. Experience with medical device testing; experience testing MicroVention products is a plus.
3. Ability to read and follow test procedures.
4. Ability to perform product inspections; ability to understand technical documentation including mechanical drawings.
5. Good computer skills especially with Word and Excel.
6. Ability to work in controlled environments (clean rooms).
7. Ability to work under pressure.
8. Teamwork skills.
**External-Facing Title:**
Sr. Technician, Supplier Quality - CR
**Posting Country:**
Outside US
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
Postúlese Ahora
Lead, Production
Alajuela
Terumo Neuro
Hoy
Trabajo visto
Descripción Del Trabajo
**13102BR**
**Title:**
Lead, Production
**Job Description:**
Coordinates production activities to ensure materials, documents and processes are compliant with the established company practices and procedures. Leads will assemble and package company's products. Assist supervisor in operations.
**Auto req ID:**
13102BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3105-Costa Rica Direct
**Qualifications:**
HS Diploma or equivalent. Knowledge of clean room procedures. Minimum 1 year experience in microscope and medical industry
**External-Facing Title:**
Lead, Production
**Posting Country:**
Outside US
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
**Title:**
Lead, Production
**Job Description:**
Coordinates production activities to ensure materials, documents and processes are compliant with the established company practices and procedures. Leads will assemble and package company's products. Assist supervisor in operations.
**Auto req ID:**
13102BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3105-Costa Rica Direct
**Qualifications:**
HS Diploma or equivalent. Knowledge of clean room procedures. Minimum 1 year experience in microscope and medical industry
**External-Facing Title:**
Lead, Production
**Posting Country:**
Outside US
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
Postúlese Ahora
Technician I, Manufacturing
Alajuela
Terumo Neuro
Hoy
Trabajo visto
Descripción Del Trabajo
**13086BR**
**Title:**
Technician I, Manufacturing
**Job Description:**
Works with engineers, supervisors and operators to support all functions related to manufacturing activities and provides training when required.
1. Works with a variety of process equipment.
2. Supports engineers in equipment or process validation studies.
3. Works under general supervision to meet production demands.
4. Identifies and repairs common equipment failures.
5. Provides operator training and monitors document conformance.
6. Identifies and corrects common process problems.
7. Supports production or process development as required.
8. Set-ups, adjusts and operates laboratory equipment and instruments
9. Drafts manufacturing documents such as work instructions, build records, validation protocols/reports, etc.
10. Builds and test validation units
11. Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
12. Perform additional duties, as assigned.
**Auto req ID:**
13086BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3215-CR-Facilities
**Qualifications:**
Required Qualifications:
1.Graduated Technical in electronics, electromechanical, mechanical, mechatronics.
2. High School Diploma
3. Associates degree in related area
4. Experience in medical device industry preferred.
**External-Facing Title:**
Technician I, Manufacturing
**Posting Country:**
Outside US
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
**Title:**
Technician I, Manufacturing
**Job Description:**
Works with engineers, supervisors and operators to support all functions related to manufacturing activities and provides training when required.
1. Works with a variety of process equipment.
2. Supports engineers in equipment or process validation studies.
3. Works under general supervision to meet production demands.
4. Identifies and repairs common equipment failures.
5. Provides operator training and monitors document conformance.
6. Identifies and corrects common process problems.
7. Supports production or process development as required.
8. Set-ups, adjusts and operates laboratory equipment and instruments
9. Drafts manufacturing documents such as work instructions, build records, validation protocols/reports, etc.
10. Builds and test validation units
11. Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
12. Perform additional duties, as assigned.
**Auto req ID:**
13086BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3215-CR-Facilities
**Qualifications:**
Required Qualifications:
1.Graduated Technical in electronics, electromechanical, mechanical, mechatronics.
2. High School Diploma
3. Associates degree in related area
4. Experience in medical device industry preferred.
**External-Facing Title:**
Technician I, Manufacturing
**Posting Country:**
Outside US
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
Postúlese Ahora
Lead, Receiving Inspection - CR (Shift B)
Alajuela
Terumo Neuro
Hoy
Trabajo visto
Descripción Del Trabajo
**13076BR**
**Title:**
Lead, Receiving Inspection - CR (Shift B)
**Job Description:**
Responsible for leading a group of QC inspectors. Support the inspection of received materials or finished product. Prepare Nonconformance Reports. Communicate with QA management, Engineering, and Operations as needed to facilitate effective inspection and manufacturing. Perform other duties as assigned by management. Job duties:
+ Support QC Inspectors in their inspection activities.
+ Set inspection priorities and ensure delivery of material on time to the production floor.
+ Prepare Nonconformance Reports and other documentation.
+ Provide input to QA Management.
+ Communicate with Engineering and Operations as needed to report issues and to improve and maintain high quality levels.
+ Provide QC support to Engineering for product development and product improvement projects.
+ Ensure product release testing is completed prior to releasing product to finished goods.
+ Ensure product pre- and post-sterilization activities are completed prior to releasing product to Finished Goods.
+ Assist in the training of QC Inspectors to documented procedures.
+ Prioritize workload based on production requirements for QC Inspectors.
+ Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
+ Perform additional duties as assigned.
**Auto req ID:**
13076BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3211-CR-Quality
**Qualifications:**
1. High School diploma or equivalent.
2. Minimum three (3) years of experience in quality control for medical device manufacturing.
3. Experience working in controlled environments areas (CEA).
4. Knowledge of technical design drawing interpretation and raw material inspection requirements.
5. Knowledge on regulations and GMPs.
6. Knowledge of computer software, including Microsoft Word, Excel, and outlook.
7. Strong written and verbal communication skills.
8. Knowledge of inspection sampling plans and standards.
9. Ability and willingness to work overtime when required.
10. Ability to understand supplier documentation (e.g., certification of conformance, material, MSDS etc.).
11. Understanding of basic metrology.
12. 60% English required.
**Desired Qualifications**
1. Ability to read and prepare technical documentation.
2. Ability to use a microscope and other inspection equipment or tools to examine components, materials and/or product/assemblies.
3. Ability to promote effective working relationships at all levels and create a positive work environment.
4. Knowledge of medical product manufacturing and quality.
**External-Facing Title:**
Lead, Receiving Inspection - CR
**Posting Country:**
Outside US
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
**Title:**
Lead, Receiving Inspection - CR (Shift B)
**Job Description:**
Responsible for leading a group of QC inspectors. Support the inspection of received materials or finished product. Prepare Nonconformance Reports. Communicate with QA management, Engineering, and Operations as needed to facilitate effective inspection and manufacturing. Perform other duties as assigned by management. Job duties:
+ Support QC Inspectors in their inspection activities.
+ Set inspection priorities and ensure delivery of material on time to the production floor.
+ Prepare Nonconformance Reports and other documentation.
+ Provide input to QA Management.
+ Communicate with Engineering and Operations as needed to report issues and to improve and maintain high quality levels.
+ Provide QC support to Engineering for product development and product improvement projects.
+ Ensure product release testing is completed prior to releasing product to finished goods.
+ Ensure product pre- and post-sterilization activities are completed prior to releasing product to Finished Goods.
+ Assist in the training of QC Inspectors to documented procedures.
+ Prioritize workload based on production requirements for QC Inspectors.
+ Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
+ Perform additional duties as assigned.
**Auto req ID:**
13076BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3211-CR-Quality
**Qualifications:**
1. High School diploma or equivalent.
2. Minimum three (3) years of experience in quality control for medical device manufacturing.
3. Experience working in controlled environments areas (CEA).
4. Knowledge of technical design drawing interpretation and raw material inspection requirements.
5. Knowledge on regulations and GMPs.
6. Knowledge of computer software, including Microsoft Word, Excel, and outlook.
7. Strong written and verbal communication skills.
8. Knowledge of inspection sampling plans and standards.
9. Ability and willingness to work overtime when required.
10. Ability to understand supplier documentation (e.g., certification of conformance, material, MSDS etc.).
11. Understanding of basic metrology.
12. 60% English required.
**Desired Qualifications**
1. Ability to read and prepare technical documentation.
2. Ability to use a microscope and other inspection equipment or tools to examine components, materials and/or product/assemblies.
3. Ability to promote effective working relationships at all levels and create a positive work environment.
4. Knowledge of medical product manufacturing and quality.
**External-Facing Title:**
Lead, Receiving Inspection - CR
**Posting Country:**
Outside US
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
Postúlese Ahora
Inspector I, Receiving - CR
Alajuela
Terumo Neuro
Hoy
Trabajo visto
Descripción Del Trabajo
**13022BR**
**Title:**
Inspector I, Receiving - CR
**Job Description:**
Responsable de la inspección y liberación de materiales en el sistema ERP. Asegurarse de la correcta preparación y liberación de productos terminados.
+ Inspección de materia prima entrante y liberación de producto terminado.
+ Asegurarse que todos los materiales/productos vayan de acuerdo con los requerimientos.
+ Asegurarse de que se realicen las pruebas de liberación de cualquier producto.
+ Brindar soporte al área de Ingeniería en el desarrollo de productos y proyectos para mejora.
+ Capaz de asistir en el auto-entrenamiento de procedimientos.
+ Realizar reportes de No Conformidad y notificar al supervisor/líder de calidad.
+ Garantizar actividades de pre & post esterilización antes de liberar el producto terminado.
+ Ejecutar y documentar aquellas inspecciones de calidad que se realicen para asegurarse que de que cumplan con las especificaciones y requerimientos de los procedimientos.
+ Brindar retro-alimentación sobre incidentes de calidad que puedan suceder a los departamentos de Calidad y Operaciones.
+ Revisar y cerrar documentación de recibido de materia prima y producto terminado.
+ Ejecutar cualquier proyecto o función que se le asigne de acuerdo a las necesidades del departamento.
+ Levantamiento de cargas y adecuado manejo de químicos.
+ Cumplir las leyes y reglamentos aplicables, adherirse a los procesos y requisitos del Sistema de Gestión de Calidad y demostrar ética e integridad en todos los asuntos y a todos los niveles de la organización.
+ Realizar las tareas adicionales que se le asignen.
**Auto req ID:**
13022BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3211-CR-Quality
**Qualifications:**
1. Título de Bachillerato.
2. Experiencia en control de calidad y recibido (deseable).
**Desired Qualifications**
1. Conocimientos generales de computación incluyendo Excel, Word, Access.
2. Buenas habilidades de comunicación, escritas y orales.
3. Responsable, completa el trabajo de una manera oportuna, y realiza tareas en forma precisa.
4. Inglés básico (deseable).
**External-Facing Title:**
Inspector I, Receiving - CR
**Posting Country:**
Outside US
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
**Title:**
Inspector I, Receiving - CR
**Job Description:**
Responsable de la inspección y liberación de materiales en el sistema ERP. Asegurarse de la correcta preparación y liberación de productos terminados.
+ Inspección de materia prima entrante y liberación de producto terminado.
+ Asegurarse que todos los materiales/productos vayan de acuerdo con los requerimientos.
+ Asegurarse de que se realicen las pruebas de liberación de cualquier producto.
+ Brindar soporte al área de Ingeniería en el desarrollo de productos y proyectos para mejora.
+ Capaz de asistir en el auto-entrenamiento de procedimientos.
+ Realizar reportes de No Conformidad y notificar al supervisor/líder de calidad.
+ Garantizar actividades de pre & post esterilización antes de liberar el producto terminado.
+ Ejecutar y documentar aquellas inspecciones de calidad que se realicen para asegurarse que de que cumplan con las especificaciones y requerimientos de los procedimientos.
+ Brindar retro-alimentación sobre incidentes de calidad que puedan suceder a los departamentos de Calidad y Operaciones.
+ Revisar y cerrar documentación de recibido de materia prima y producto terminado.
+ Ejecutar cualquier proyecto o función que se le asigne de acuerdo a las necesidades del departamento.
+ Levantamiento de cargas y adecuado manejo de químicos.
+ Cumplir las leyes y reglamentos aplicables, adherirse a los procesos y requisitos del Sistema de Gestión de Calidad y demostrar ética e integridad en todos los asuntos y a todos los niveles de la organización.
+ Realizar las tareas adicionales que se le asignen.
**Auto req ID:**
13022BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3211-CR-Quality
**Qualifications:**
1. Título de Bachillerato.
2. Experiencia en control de calidad y recibido (deseable).
**Desired Qualifications**
1. Conocimientos generales de computación incluyendo Excel, Word, Access.
2. Buenas habilidades de comunicación, escritas y orales.
3. Responsable, completa el trabajo de una manera oportuna, y realiza tareas en forma precisa.
4. Inglés básico (deseable).
**External-Facing Title:**
Inspector I, Receiving - CR
**Posting Country:**
Outside US
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
Postúlese Ahora
Inspector I, Receiving - CR
Alajuela
Terumo Neuro
Hoy
Trabajo visto
Descripción Del Trabajo
**13881BR**
**Title:**
Inspector I, Receiving - CR
**Job Description:**
Responsable de la inspección y liberación de materiales en el sistema ERP. Asegurarse de la correcta preparación y liberación de productos terminados.
+ Inspección de materia prima entrante y liberación de producto terminado.
+ Asegurarse que todos los materiales/productos vayan de acuerdo con los requerimientos.
+ Asegurarse de que se realicen las pruebas de liberación de cualquier producto.
+ Brindar soporte al área de Ingeniería en el desarrollo de productos y proyectos para mejora.
+ Capaz de asistir en el auto-entrenamiento de procedimientos.
+ Realizar reportes de No Conformidad y notificar al supervisor/líder de calidad.
+ Garantizar actividades de pre & post esterilización antes de liberar el producto terminado.
+ Ejecutar y documentar aquellas inspecciones de calidad que se realicen para asegurarse que de que cumplan con las especificaciones y requerimientos de los procedimientos.
+ Brindar retro-alimentación sobre incidentes de calidad que puedan suceder a los departamentos de Calidad y Operaciones.
+ Revisar y cerrar documentación de recibido de materia prima y producto terminado.
+ Ejecutar cualquier proyecto o función que se le asigne de acuerdo a las necesidades del departamento.
+ Levantamiento de cargas y adecuado manejo de químicos.
+ Cumplir las leyes y reglamentos aplicables, adherirse a los procesos y requisitos del Sistema de Gestión de Calidad y demostrar ética e integridad en todos los asuntos y a todos los niveles de la organización.
+ Realizar las tareas adicionales que se le asignen.
**Auto req ID:**
13881BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3211-CR-Quality
**Qualifications:**
1. Título de Bachillerato.
2. Experiencia en control de calidad y recibido (deseable).
**Desired Qualifications**
1. Conocimientos generales de computación incluyendo Excel, Word, Access.
2. Buenas habilidades de comunicación, escritas y orales.
3. Responsable, completa el trabajo de una manera oportuna, y realiza tareas en forma precisa.
4. Inglés básico (deseable).
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
**Title:**
Inspector I, Receiving - CR
**Job Description:**
Responsable de la inspección y liberación de materiales en el sistema ERP. Asegurarse de la correcta preparación y liberación de productos terminados.
+ Inspección de materia prima entrante y liberación de producto terminado.
+ Asegurarse que todos los materiales/productos vayan de acuerdo con los requerimientos.
+ Asegurarse de que se realicen las pruebas de liberación de cualquier producto.
+ Brindar soporte al área de Ingeniería en el desarrollo de productos y proyectos para mejora.
+ Capaz de asistir en el auto-entrenamiento de procedimientos.
+ Realizar reportes de No Conformidad y notificar al supervisor/líder de calidad.
+ Garantizar actividades de pre & post esterilización antes de liberar el producto terminado.
+ Ejecutar y documentar aquellas inspecciones de calidad que se realicen para asegurarse que de que cumplan con las especificaciones y requerimientos de los procedimientos.
+ Brindar retro-alimentación sobre incidentes de calidad que puedan suceder a los departamentos de Calidad y Operaciones.
+ Revisar y cerrar documentación de recibido de materia prima y producto terminado.
+ Ejecutar cualquier proyecto o función que se le asigne de acuerdo a las necesidades del departamento.
+ Levantamiento de cargas y adecuado manejo de químicos.
+ Cumplir las leyes y reglamentos aplicables, adherirse a los procesos y requisitos del Sistema de Gestión de Calidad y demostrar ética e integridad en todos los asuntos y a todos los niveles de la organización.
+ Realizar las tareas adicionales que se le asignen.
**Auto req ID:**
13881BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3211-CR-Quality
**Qualifications:**
1. Título de Bachillerato.
2. Experiencia en control de calidad y recibido (deseable).
**Desired Qualifications**
1. Conocimientos generales de computación incluyendo Excel, Word, Access.
2. Buenas habilidades de comunicación, escritas y orales.
3. Responsable, completa el trabajo de una manera oportuna, y realiza tareas en forma precisa.
4. Inglés básico (deseable).
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
Postúlese Ahora
Inspector I, Quality Control - CR-1
Alajuela
Terumo Neuro
Hoy
Trabajo visto
Descripción Del Trabajo
**13795BR**
**Title:**
Inspector I, Quality Control - CR-1
**Job Description:**
Ejecutar inspecciones en varias etapas de producción de los dispositivos, desde las materias primas, subensambles y ensambles finales para asegurar la calidad y conformidad con las especificaciones y requerimientos de los procedimientos. Asimismo, revisar el registro de historial de manufactura del dispositivo para asegurar el cumplimiento y asistir en la preparación y liberación del producto empacado y producto final.
+ Ejecutar y documentar las inspecciones de Calidad para asegurar la conformidad con las especificaciones y requerimientos de los procedimientos.
+ Suministrar la retroalimentación a los departamentos de Calidad y Operaciones acerca de los incidentes de calidad.
+ Ejecutar, revisar y cerrar registros de producción (Build Records).
+ Inspeccionar producto en proceso y producto final empacado.
+ Inspeccionar material asociado a yellow sheets, ordenes de ingeniería, retrabajos, etc.
+ Cumplir las leyes y reglamentos aplicables, adherirse a los procesos y requisitos del Sistema de Gestión de Calidad y demostrar ética e integridad en todos los asuntos y a todos los niveles de la organización.
+ Realizar las tareas adicionales que se le asignen.
**Auto req ID:**
13795BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3211-CR-Quality
**Qualifications:**
1. Bachiller en Educación Media.
2. Experiencia previa trabajando con microscopios.
3. Buenas habilidades de comunicación escrita y verbal.
4. Ingles Nivel A1.
**Desired Qualifications**
1. Un (1) año de experiencia en manufactura de dispositivos médicos o similar.
2. Experiencia previa con equipo de inspección por medio de video y herramientas adicionales de inspección.
3. Conocimiento demostrado en técnicas de inspección, lectura y comprensión de documentación técnica que incluye planos.
4. Habilidad para trabajar en ambientes controlados (Cuartos limpios).
5. Enfoque en los detalles.
6. Buenas habilidades interpersonales.
7. Conocimiento de Buenas prácticas de manufactura (GMPs) y de regulaciones de calidad de industria médica (Quality System Regulation QSR y/o International Organization for Standardization ISO).
8. Conocimiento de Buenas prácticas de documentación (GDPs).
9. Conocimiento en software de computación, incluyendo Microsoft Word y Excel.
10. Habilidad para trabajar en un ambiente de trabajo dinámico y de ejecución de cambios y movimientos con rapidez, y de balancear y priorizar cargas de trabajo para el soporte al planeamiento de producción.
**Physical**
1. Levantamiento moderado de peso.
2. Periodos largos de uso de microscopios.
3. Periodos largos de estar sentado, caminando o de pie.
4. Es posible que el puesto requiera trabajar en un entorno en el que se pueda estar expuesto a la radiación (como en los laboratorios de cateterismo).
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
**Title:**
Inspector I, Quality Control - CR-1
**Job Description:**
Ejecutar inspecciones en varias etapas de producción de los dispositivos, desde las materias primas, subensambles y ensambles finales para asegurar la calidad y conformidad con las especificaciones y requerimientos de los procedimientos. Asimismo, revisar el registro de historial de manufactura del dispositivo para asegurar el cumplimiento y asistir en la preparación y liberación del producto empacado y producto final.
+ Ejecutar y documentar las inspecciones de Calidad para asegurar la conformidad con las especificaciones y requerimientos de los procedimientos.
+ Suministrar la retroalimentación a los departamentos de Calidad y Operaciones acerca de los incidentes de calidad.
+ Ejecutar, revisar y cerrar registros de producción (Build Records).
+ Inspeccionar producto en proceso y producto final empacado.
+ Inspeccionar material asociado a yellow sheets, ordenes de ingeniería, retrabajos, etc.
+ Cumplir las leyes y reglamentos aplicables, adherirse a los procesos y requisitos del Sistema de Gestión de Calidad y demostrar ética e integridad en todos los asuntos y a todos los niveles de la organización.
+ Realizar las tareas adicionales que se le asignen.
**Auto req ID:**
13795BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3211-CR-Quality
**Qualifications:**
1. Bachiller en Educación Media.
2. Experiencia previa trabajando con microscopios.
3. Buenas habilidades de comunicación escrita y verbal.
4. Ingles Nivel A1.
**Desired Qualifications**
1. Un (1) año de experiencia en manufactura de dispositivos médicos o similar.
2. Experiencia previa con equipo de inspección por medio de video y herramientas adicionales de inspección.
3. Conocimiento demostrado en técnicas de inspección, lectura y comprensión de documentación técnica que incluye planos.
4. Habilidad para trabajar en ambientes controlados (Cuartos limpios).
5. Enfoque en los detalles.
6. Buenas habilidades interpersonales.
7. Conocimiento de Buenas prácticas de manufactura (GMPs) y de regulaciones de calidad de industria médica (Quality System Regulation QSR y/o International Organization for Standardization ISO).
8. Conocimiento de Buenas prácticas de documentación (GDPs).
9. Conocimiento en software de computación, incluyendo Microsoft Word y Excel.
10. Habilidad para trabajar en un ambiente de trabajo dinámico y de ejecución de cambios y movimientos con rapidez, y de balancear y priorizar cargas de trabajo para el soporte al planeamiento de producción.
**Physical**
1. Levantamiento moderado de peso.
2. Periodos largos de uso de microscopios.
3. Periodos largos de estar sentado, caminando o de pie.
4. Es posible que el puesto requiera trabajar en un entorno en el que se pueda estar expuesto a la radiación (como en los laboratorios de cateterismo).
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
Postúlese Ahora
Engineer Sr, Supplier Quality - CR
Alajuela
Terumo Neuro
Hoy
Trabajo visto
Descripción Del Trabajo
**13887BR**
**Title:**
Engineer Sr, Supplier Quality - CR
**Job Description:**
Work in a team environment with suppliers to develop and implement best practices that emphasize defect prevention and reduction in variation and waste and provide for continuous improvements in meeting all customer requirements. Investigate, analyze, and resolve supplier quality issues by conducting audits, manufacturing line assessments, analyzing defect trends, and leading continuous improvement projects. Manage customer specific requirements and offer technical support to suppliers. Responsible for ensuring that the products meet quality standards required to minimize quality costs and maximize customer satisfaction whilst ensuring that procedures and processes are adhered to. Act as a partner in developing key suppliers (second sourcing) to meet the company's stringent quality requirements. Job duties:
+ Perform analysis and identify trends in the inspection of finished products, in-process materials, raw materials, and recommend corrective actions when necessary.
+ Perform problem solving and root cause analysis activities with suppliers and customers to eliminate recurrence of defects.
+ Utilize process improvement tools to drive process and product quality.
+ Monitor supplier quality levels and perform development activities with strategic suppliers to ensure quality performance goals are met.
+ Perform supplier re-evaluations based on company requirements.
+ Initiate action at the RI lab or manufacturing lines to prevent the occurrence of any non‐conformities relating to product, process, and quality systems.
+ Maintain approved supplier list updates based on company requirements.
+ Perform supplier quality audits.
+ Develop projects to improve RI and Release capabilities.
+ Develop and execute Test Method validations for RI and Release inspections.
+ Develop and execute Software and equipment validations.
+ Supplier process qualification - ensure supplier adherence to Work Instructions, Process Control Plans, Engineering Drawings, and Specifications.
+ Work closely with suppliers and R&D, Supply Chain, and Quality Engineering groups to ensure potential suppliers (second sourcing) for development projects meet requirements for qualification.
+ Generate a monthly Supplier Performance Report including input from NCRs, SCARs, and supplier ratings.
+ Manage supplier change notifications.
+ Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
+ Perform additional duties as assigned.
**Auto req ID:**
13887BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3211-CR-Quality
**Qualifications:**
1. Bachelor's degree in engineering related field or equivalent, and at least 40% of studies on advanced degree.
2. Minimum of four (4) years of experience in a quality engineering role.
3. Minimum of four (4) years of experience medical device industry or related field.
4. Strong written and verbal communication skills.
5. Expertise/experience in root cause analysis, corrective/preventive action methods, and problem solving with quality tools such as Six Sigma / 8-D/ CAPA / FMEA / 5 WHYs, etc.
6. Understanding and interpretation of engineering drawings.
7. 80% English proficiency both written and verbal.
8. Proficient with MS Word, Excel, Outlook, and Teams.
**Desired Qualifications**
1. Advanced degree completed, and/or 40% career progress.
2. Lead Auditor of ISO13485 or equivalent preferred.
3. Solid understanding of receiving inspection and finish product release processes including statistical sampling, test method validation, component measurement techniques, specifications, sterilization, and drawings.
4. Quality Certification or training on CQE, SSGB, or equivalent.
5. Working knowledge of appropriate global medical device regulations, requirements, and standards such as ISO 9001, ISO13485, QSR, MDD preferred.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
**Title:**
Engineer Sr, Supplier Quality - CR
**Job Description:**
Work in a team environment with suppliers to develop and implement best practices that emphasize defect prevention and reduction in variation and waste and provide for continuous improvements in meeting all customer requirements. Investigate, analyze, and resolve supplier quality issues by conducting audits, manufacturing line assessments, analyzing defect trends, and leading continuous improvement projects. Manage customer specific requirements and offer technical support to suppliers. Responsible for ensuring that the products meet quality standards required to minimize quality costs and maximize customer satisfaction whilst ensuring that procedures and processes are adhered to. Act as a partner in developing key suppliers (second sourcing) to meet the company's stringent quality requirements. Job duties:
+ Perform analysis and identify trends in the inspection of finished products, in-process materials, raw materials, and recommend corrective actions when necessary.
+ Perform problem solving and root cause analysis activities with suppliers and customers to eliminate recurrence of defects.
+ Utilize process improvement tools to drive process and product quality.
+ Monitor supplier quality levels and perform development activities with strategic suppliers to ensure quality performance goals are met.
+ Perform supplier re-evaluations based on company requirements.
+ Initiate action at the RI lab or manufacturing lines to prevent the occurrence of any non‐conformities relating to product, process, and quality systems.
+ Maintain approved supplier list updates based on company requirements.
+ Perform supplier quality audits.
+ Develop projects to improve RI and Release capabilities.
+ Develop and execute Test Method validations for RI and Release inspections.
+ Develop and execute Software and equipment validations.
+ Supplier process qualification - ensure supplier adherence to Work Instructions, Process Control Plans, Engineering Drawings, and Specifications.
+ Work closely with suppliers and R&D, Supply Chain, and Quality Engineering groups to ensure potential suppliers (second sourcing) for development projects meet requirements for qualification.
+ Generate a monthly Supplier Performance Report including input from NCRs, SCARs, and supplier ratings.
+ Manage supplier change notifications.
+ Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
+ Perform additional duties as assigned.
**Auto req ID:**
13887BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3211-CR-Quality
**Qualifications:**
1. Bachelor's degree in engineering related field or equivalent, and at least 40% of studies on advanced degree.
2. Minimum of four (4) years of experience in a quality engineering role.
3. Minimum of four (4) years of experience medical device industry or related field.
4. Strong written and verbal communication skills.
5. Expertise/experience in root cause analysis, corrective/preventive action methods, and problem solving with quality tools such as Six Sigma / 8-D/ CAPA / FMEA / 5 WHYs, etc.
6. Understanding and interpretation of engineering drawings.
7. 80% English proficiency both written and verbal.
8. Proficient with MS Word, Excel, Outlook, and Teams.
**Desired Qualifications**
1. Advanced degree completed, and/or 40% career progress.
2. Lead Auditor of ISO13485 or equivalent preferred.
3. Solid understanding of receiving inspection and finish product release processes including statistical sampling, test method validation, component measurement techniques, specifications, sterilization, and drawings.
4. Quality Certification or training on CQE, SSGB, or equivalent.
5. Working knowledge of appropriate global medical device regulations, requirements, and standards such as ISO 9001, ISO13485, QSR, MDD preferred.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
Postúlese Ahora
Buyer II - CR
Alajuela
Terumo Neuro
Hoy
Trabajo visto
Descripción Del Trabajo
**13885BR**
**Title:**
Buyer II - CR
**Job Description:**
The Buyer II performs and coordinates the scheduling, planning, procurement and expediting for specific product lines to meet master schedule and customer order requirements. This position is also responsible for maintaining inventory levels supporting production/R&D and customer requirements, while maintaining economic control of inventories. Job duties:
+ Supports new product development by coordinating supplier's input during the development period and leads negotiation for desired results and purchase validation materials.
+ Establishes and maintains supplier relations and partnerships.
+ Develops and identifies supply sources and alternatives that are relevant to the needs of the business.
+ Must be able to collect, analyze and interpret manufacturing data in order to make decisions that may impact production, staff or processes.
+ Identifies and implements cost savings/cost avoidance opportunities.
+ Reviews and processes purchase requisitions and purchase orders while implementing procurement strategies, policies and procedures, while successfully managing risks.
+ Serves as the key point of contact for authorized requesters, managers and suppliers to troubleshoot and resolve purchase requisition and purchase order issues.
+ Must be able to prioritize own assignments, while focusing on key tasks despite limited time and resources.
+ Resolves quality, pricing and delivery issues with suppliers.
+ Interfaces with Accounts Payable and internal customers to resolve invoice and receiving discrepancies.
+ Must possess the ability to maintain projects and critical tasks progressing when delays or problems occur.
+ Accepts the responsibility of a leadership role in improving processes.
+ Works under minimal supervision while assisting less experienced peers.
+ Additional duties and responsibilities as assigned.
**Auto req ID:**
13885BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
100-General and Administrative
**Qualifications:**
1. Bachelor's Degree in Business or a technical field preferred.
2. Three to five years of experience in a manufacturing environment.
3. Medical Device manufacturing experience preferred.
4. APICS or other industry certification(s) a plus.
**Desired Qualifications**
1. Strong Knowledge of ERP/MRP Systems, BOM and planning skills.
2. Project management experience and strong organizational skills.
3. Tactical experience with lean principles, supply chain management including material flow and delivery applications.
4. Must have a good understanding of manufacturing, purchasing, scheduling and planning processes.
5. Strong analytical, problem solving and negotiating skills.
6. Knowledge of medical device associated supply base a plus.
7. Experience with developing & implementing ordering policies.
8. Must possess excellent interpersonal skills to build and enhance solid working relationships that promote collaboration and cooperation with all levels of the company and suppliers.
9. Must be able to problem solve and think independently in a constantly changing production environment.
10. Possesses sound judgment and exceptional time management skills.
11. Proficient with MS Word, Excel, Access and Outlook.
**External-Facing Title:**
Buyer II - CR
**Posting Country:**
Outside US
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
**Title:**
Buyer II - CR
**Job Description:**
The Buyer II performs and coordinates the scheduling, planning, procurement and expediting for specific product lines to meet master schedule and customer order requirements. This position is also responsible for maintaining inventory levels supporting production/R&D and customer requirements, while maintaining economic control of inventories. Job duties:
+ Supports new product development by coordinating supplier's input during the development period and leads negotiation for desired results and purchase validation materials.
+ Establishes and maintains supplier relations and partnerships.
+ Develops and identifies supply sources and alternatives that are relevant to the needs of the business.
+ Must be able to collect, analyze and interpret manufacturing data in order to make decisions that may impact production, staff or processes.
+ Identifies and implements cost savings/cost avoidance opportunities.
+ Reviews and processes purchase requisitions and purchase orders while implementing procurement strategies, policies and procedures, while successfully managing risks.
+ Serves as the key point of contact for authorized requesters, managers and suppliers to troubleshoot and resolve purchase requisition and purchase order issues.
+ Must be able to prioritize own assignments, while focusing on key tasks despite limited time and resources.
+ Resolves quality, pricing and delivery issues with suppliers.
+ Interfaces with Accounts Payable and internal customers to resolve invoice and receiving discrepancies.
+ Must possess the ability to maintain projects and critical tasks progressing when delays or problems occur.
+ Accepts the responsibility of a leadership role in improving processes.
+ Works under minimal supervision while assisting less experienced peers.
+ Additional duties and responsibilities as assigned.
**Auto req ID:**
13885BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
100-General and Administrative
**Qualifications:**
1. Bachelor's Degree in Business or a technical field preferred.
2. Three to five years of experience in a manufacturing environment.
3. Medical Device manufacturing experience preferred.
4. APICS or other industry certification(s) a plus.
**Desired Qualifications**
1. Strong Knowledge of ERP/MRP Systems, BOM and planning skills.
2. Project management experience and strong organizational skills.
3. Tactical experience with lean principles, supply chain management including material flow and delivery applications.
4. Must have a good understanding of manufacturing, purchasing, scheduling and planning processes.
5. Strong analytical, problem solving and negotiating skills.
6. Knowledge of medical device associated supply base a plus.
7. Experience with developing & implementing ordering policies.
8. Must possess excellent interpersonal skills to build and enhance solid working relationships that promote collaboration and cooperation with all levels of the company and suppliers.
9. Must be able to problem solve and think independently in a constantly changing production environment.
10. Possesses sound judgment and exceptional time management skills.
11. Proficient with MS Word, Excel, Access and Outlook.
**External-Facing Title:**
Buyer II - CR
**Posting Country:**
Outside US
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
Postúlese Ahora
Coordinator I, Production Training - CR
Alajuela
Terumo Neuro
Hoy
Trabajo visto
Descripción Del Trabajo
**13854BR**
**Title:**
Coordinator I, Production Training - CR
**Job Description:**
Mantiene la base de datos, y proporciona material de entrenamiento para todos los asociados de producción. Mantiene archivos de entrenamientos en conformidad con el Sistema de Calidad como lo establece la compañía. Job duties:
+ Actualizar la matriz de entrenamientos.
+ Actualizar archivos de entrenamiento.
+ Realizar entrenamientos cuando se dé cambio en SOPs/WIs.
+ Enviar notificación a supervisores, líderes y entrenadores de próximas recertificaciones.
+ Coordinar con ingenieros y entrenadores los entrenamientos de MP's, PD's, CF's, BR's, entre otros.
+ Llevar un registro de los entrenamientos pendientes.
+ Revisar que la documentación cumpla con los GDP's.
+ Mantener inventario de documentos controlados en las líneas de producción (MP's, PD's).
+ Realizar auditorías de los documentos contra la matriz de los entrenamientos.
+ Realizar auditorías de los inventarios de documentos en las líneas de producción.
+ Colaborar a los ingenieros, supervisores y líderes con investigaciones necesarias relacionadas a entrenamientos.
+ Preparar material para entrenamientos.
+ Actualizar matriz de training files.
+ Archivar paquetes de entrenamiento y training files.
+ Impartir inducción cuando sea necesario.
+ Cumplir con las Leyes y Reglamentos aplicables, adherirse a los procesos y requisitos del Sistema de Gestión de Calidad, así como demostrar Ética e Integridad en todos los asuntos y en todos los niveles de la organización.
+ Realizar tareas adicionales, según lo asignado.
**Auto req ID:**
13854BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3105-Costa Rica Direct
**Qualifications:**
1. Bachiller en educación media deseable.
2. 1 a 2 años de experiencia relacionada con el cargo y el área.
3. Manejo de regulaciones de "Cuarto Limpio", buenas prácticas de manufactura (GMP's) y buenas prácticas de documentación (GDP's).
4. Manejo de Microsoft Office.
5. Experiencia en trabajo de ensamble bajo microscopio en empresa de dispositivos médicos.
**Desired Qualifications**
1. Poseer buenas habilidades de comunicación para transmitir conocimientos de forma eficiente.
2. Dar entrenamientos efectivos.
3. Proporcionar información a los supervisores en relación con los problemas de producción y avance de los entrenamientos.
4. Capacidad de seguir los procedimientos de la empresa. Ser modelo a seguir.
5. Proactivo, analítico y ordenado.
6. Capacidad para trabajar con supervisión moderada.
**Physical**
+ Periodos prolongados de pie.
+ Períodos prolongados sentado.
+ Capacidad para levantar, empujar o jalar hasta 50 libras ocasionalmente y hasta 15 libras con frecuencia .
+ Periodo prolongado del uso de computadora.
+ Es posible que el puesto requiera trabajar en un entorno en el que se pueda estar expuesto a la radiación (como en los laboratorios de cateterismo).
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
**Title:**
Coordinator I, Production Training - CR
**Job Description:**
Mantiene la base de datos, y proporciona material de entrenamiento para todos los asociados de producción. Mantiene archivos de entrenamientos en conformidad con el Sistema de Calidad como lo establece la compañía. Job duties:
+ Actualizar la matriz de entrenamientos.
+ Actualizar archivos de entrenamiento.
+ Realizar entrenamientos cuando se dé cambio en SOPs/WIs.
+ Enviar notificación a supervisores, líderes y entrenadores de próximas recertificaciones.
+ Coordinar con ingenieros y entrenadores los entrenamientos de MP's, PD's, CF's, BR's, entre otros.
+ Llevar un registro de los entrenamientos pendientes.
+ Revisar que la documentación cumpla con los GDP's.
+ Mantener inventario de documentos controlados en las líneas de producción (MP's, PD's).
+ Realizar auditorías de los documentos contra la matriz de los entrenamientos.
+ Realizar auditorías de los inventarios de documentos en las líneas de producción.
+ Colaborar a los ingenieros, supervisores y líderes con investigaciones necesarias relacionadas a entrenamientos.
+ Preparar material para entrenamientos.
+ Actualizar matriz de training files.
+ Archivar paquetes de entrenamiento y training files.
+ Impartir inducción cuando sea necesario.
+ Cumplir con las Leyes y Reglamentos aplicables, adherirse a los procesos y requisitos del Sistema de Gestión de Calidad, así como demostrar Ética e Integridad en todos los asuntos y en todos los niveles de la organización.
+ Realizar tareas adicionales, según lo asignado.
**Auto req ID:**
13854BR
**Location MV:**
Alajuela, Costa Rica
**Department Name:**
3105-Costa Rica Direct
**Qualifications:**
1. Bachiller en educación media deseable.
2. 1 a 2 años de experiencia relacionada con el cargo y el área.
3. Manejo de regulaciones de "Cuarto Limpio", buenas prácticas de manufactura (GMP's) y buenas prácticas de documentación (GDP's).
4. Manejo de Microsoft Office.
5. Experiencia en trabajo de ensamble bajo microscopio en empresa de dispositivos médicos.
**Desired Qualifications**
1. Poseer buenas habilidades de comunicación para transmitir conocimientos de forma eficiente.
2. Dar entrenamientos efectivos.
3. Proporcionar información a los supervisores en relación con los problemas de producción y avance de los entrenamientos.
4. Capacidad de seguir los procedimientos de la empresa. Ser modelo a seguir.
5. Proactivo, analítico y ordenado.
6. Capacidad para trabajar con supervisión moderada.
**Physical**
+ Periodos prolongados de pie.
+ Períodos prolongados sentado.
+ Capacidad para levantar, empujar o jalar hasta 50 libras ocasionalmente y hasta 15 libras con frecuencia .
+ Periodo prolongado del uso de computadora.
+ Es posible que el puesto requiera trabajar en un entorno en el que se pueda estar expuesto a la radiación (como en los laboratorios de cateterismo).
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.
Postúlese Ahora