Merit Medical

Merit Medical

Merit medical is a leading manufacturer of medical devices.

Giro

Manufacturera

Actividad principal

Merit medical is a leading manufacturer of medical devices.

Número de empleados

1300

Sitio Web corporativo

Información

Founded in 1987, Merit Medical Systems, Inc. is a worldwide company engaged in the development, manufacture and distribution of proprietary disposable medical devices used in interventional and diagnostic procedures, particularly in cardiology, radiology and endoscopy.

11 puestos de Trabajo

Líder de Producción III

RESUMEN DE LAS CUALIFICACIONES MÍNIMAS • Educación y experiencia equivalentes a un certificado de preparatoria o certificado de estudios de preparatoria, con estudios universitarios de preferencia. • Un mínimo de dos años de experiencia en trabajos relacionados con las operaciones de ensamble y fabricación en industria médica (requerido haber trabajado en ambientes controlados/cuartos limpios) • En las oficinas corporativas, si este puesto es en español, se deben demostrar habilidades bilingües (inglés/español) básicas de habla, lectura y redacción. • Demostrar lo siguiente: • Cumplir los tiempos de ensamble programados mientras se cumplen las buenas prácticas de calidad. • Habilidades interpersonales, capacidad para delegar y trabajar bien como parte del equipo de ensamble. • Capacitar en las habilidades de ensamble y motivar a los trabajadores en el desarrollo del desempeño en equipo. • Atención a los detalles y buenas habilidades de organización. • Habilidades en la resolución de problemas y manejo de conflictos. • Habilidades básicas en lectura, redacción y comprensión en inglés. • Seguir instrucciones escritas y orales. • Demostrar competencias informáticas, de preferencia en hojas de cálculo, procesamiento de textos, bases de datos y otros programas de software que aplican. COMPETENCIAS • Priorización de órdenes de trabajo. • Priorización del trabajo. • Proceso de ensamble/especificaciones de calidad. • Capacitación. • Presentación de informes de producción. • Resolución de problemas con el equipo/trabajo en equipo. • Normas/procesos de producción. COMENTARIOS Riesgo de control de infecciones categoría III: La categoría de riesgos explica si los empleados tienen la posibilidad de tener contacto con los líquidos corporales o con la sangre mientras realizan su trabajo. La categoría de riesgos III establece empleos y procedimientos que no implican exposición.

Julio 24 2026 en Tijuana

Sr Quality Assurance Engineer I (temporary 4 months)

MINIMUM QUALIFICATIONS • Education and/or experience equivalent to a Bachelor's Degree in Engineering or related field with six years of quality engineering experience (to include experience in the development and implementation of effective quality systems). • Advanced English level • Prior medical indsutry experience • Strong interpersonal, organizational, and verbal and written communication skills and the ability to work effectively as a team member. • Demonstrated working knowledge of 21 CFR 820 (Quality Systems Medical Devices), ISO 13485, ISO14791, and other medical device related standards. • Proven ability to work effectively in a team environment through conflict resolution and negotiations. • Working knowledge of statistical methodologies, quality control and manufacturing tools, such as applied statistics, lean manufacturing, Six Sigma, etc. • Knowledge of applicable regulatory agency regulations. • Demonstrated computer skills preferably spreadsheets, word processing, database and other applicable software programs. PREFERRED QUALIFICATIONS • Medical device experience or equivalent experience in a regulated industry. • Experience handling deviations, investigations and CAPAs. • Experience with MasterControl, SmartCAPA, Oracle and Crystal. COMPETENCIES • Engineering problem solving/decision making • Technician supervision • Special projects/ECN's/prototype creation • NC causes/corrective actions/dispositions COMMENTS Infectious Control Risk Category II: The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs. Risk category II states employment and procedures that may require exposure.

Julio 24 2026 en Tijuana

Operations Supervisor II

SUMMARY OF MINIMUM QUALIFICATIONS • Education and/or experience equivalent to a related Bachelor's Degree. • A minimum of three years of supervisory experience, preferably in a related manufacturing environment and demonstrated ability to supervise others in a team atmosphere. • Conversational English level (preferred) • Prior medical industry experience (clean room specifically) • Availability to work from Monday to Thursday from 6:30 am to 6:30 pm • Experience managing teams up to 80-100 people • Lean projects prior experience • At the Corporate site, if this position is on a Spanish-language line, bilingual (English/Spanish) basic speaking, reading and writing skills must be demonstrated. • Excellent analytical skills, including the ability to identify improvements in manufacturing methods and processes. • Ability to plan and organize production schedules to complete work orders on a timely basis and ensure that each work order is properly filled. • Ability to communicate effectively with others orally. • Demonstrated computer skills preferably spreadsheets, word processing, database and other applicable software programs. COMPETENCIES • Production supervisory process/work assigning/paperwork/clean room maintenance/quality standards • Personnel supervisory process/performance process/transfers/status changes/salary/ hiring/discipline • Product quality • Teamwork production/profitability goals • Train production method/safety/cleanliness standards COMMENTS Infectious Control Risk Category III: The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs. Risk category III states employment and procedures that do not require exposure.

Julio 24 2026 en Tijuana

Quality Assurance Engineer II (Molding)

SUMMARY OF MINIMUM QUALIFICATIONS • Education and/or experience equivalent to a Bachelor's Degree in Engineering or related field with three years quality engineering experience in medical devices. • Prior medical industry experience • Advanced English level • Strong interpersonal, organizational, and verbal and written communication skills and the ability to work effectively as a team member. • Demonstrated working knowledge of 21 CFR 820 (Quality Systems Medical Devices), ISO 13485, ISO14791, and other medical device related standards. • Proven ability to work effectively in a team environment through conflict resolution and negotiations. • Working knowledge of statistical methodologies, quality control and manufacturing tools, such as applied statistics, lean manufacturing, Six Sigma, etc. • Demonstrated computer skills preferably spreadsheets, word processing, database and other applicable software programs. PREFERRED QUALIFICATIONS • Medical device experience or equivalent experience in a regulated industry. • Experience handling non-conformances, deviations, investigations and CAPAs. • Experience in revieweing and approving validations for molded products. COMPETENCIES • Engineering techniques/evaluation/selection/application • Engineering variable analysis • Plans/surveys/structures/equipment • Supervisory assistance • Special projects/ECN's/prototype creation • NC causes/corrective actions/dispositions COMMENTS Infectious Control Risk Category II: The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs. Risk category II states employment and procedures that may require exposure.

Julio 24 2026 en Tijuana