Sonova

Sonova

Proveedor de soluciones de cuidado auditivo - Dispositivos Médicos

Giro

Manufacturera

Actividad principal

Proveedor de soluciones de cuidado auditivo - Dispositivos Médicos

Número de empleados

800

Información

Sonova, con sede central en Stafa (Suiza), es un proveedor líder en el mercado global de soluciones innovadoras del cuidado auditivo. En una vida sin sonido, nuestro trabajo aporta sentido, no somos sólo una empresa que fabrica productos: SOMOS UN EQUIPO CON LA MISION DE AYUDAR A LAS PERSONAS A DISFRUTAR DEL PLACER DE ESCUCHAR, PARA HACER POSIBLE UNA VIDA SIN LIMITACIONES. A traves de nuestras marcas, desarrollamos, fabricamos y distribuimos soluciones que superan los límites de la tecnología y redefinen el futuro de nuestro sector. Esta diversidad les permite a nuestros usuarios finales beneficiarse de nuestra amplia gama de soluciones (Audífonos, implantes cocleares, productos de comunicación inalámbrica, soluciones digitales y atención audiológica profesional) de la forma que mejor se adapte a sus necesidades individuales.

7 puestos de Trabajo

Production Supervisor / Advanced Bionics

Experience and Requirements Bachelor’s degree in Engineering, preferably in Industrial, Electronics, Mechanical, Electrical, Mechatronics, or Biomedical Engineering. Minimum of 3–5 years of experience supervising manufacturing assembly lines, preferably within the medical device and/or electronics manufacturing industry. Valid B1/B2 visa for travel to the United States. Demonstrated ability to take a leadership role, particularly when conducting production meetings and coordinating activities with Engineering, Planning, Quality Assurance (QA), and Research & Development (R&D). Experience performing production capacity analysis and generating reports to support production scheduling decisions and respond to operational requirements. Experience leading production meetings focused on performance metrics, floor training, production priorities, and Quality Improvement Teams (QIT). Knowledge of Line Clearance procedures and regulatory compliance requirements applicable to medical device manufacturing, including FDA 21 CFR requirements. Strong understanding of production schedules, material handling, inventory flow, and Lean Manufacturing principles. Experience working with ERP systems, preferably Dataflo, as well as Microsoft Access, Word, and Excel. Strong analytical, organizational, communication, and problem-solving skills. Ability to work effectively in a fast-paced manufacturing environment and collaborate with cross-functional teams. Preferred Qualifications APICS certification or related supply chain/manufacturing certification. Experience working in a Lean Manufacturing environment. Previous experience in an FDA-regulated manufacturing environment, preferably within the medical device industry. Experience with soldering, welding, or similar assembly processes. Experience with continuous improvement methodologies such as DMAIC, Kaizen, or Six Sigma.

Octubre 16 2026 en Mexicali

Process Engineer

Qualifications & Skills: Bachelor’s degree in Industrial, Mechanical, or Electrical Engineering. Solid knowledge of FDA QSR regulations; experience with ISO 13485 standards is strongly preferred. Minimum of 3 years of experience in a similar manufacturing or process engineering role. Proven experience creating and maintaining process work instructions for manufacturing operations, including assembly and in-process acceptance procedures. Proficient in developing and executing Process Validation Protocols and/or Transfer Plans, including generating comprehensive test reports. Skilled in process risk assessments, including pFMEA development and maintenance. Supports investigation, disposition, and implementation of corrective actions for non-conforming materials. Experience establishing and monitoring statistical process controls (SPC) in production environments. Strong attention to detail and ability to work independently or collaboratively in cross-functional teams. Demonstrated problem-solving abilities with a structured and data-driven approach. Proficient in Microsoft Office Suite; working knowledge of Corel Draw. Soft Skills & Competencies: High learning agility and adaptability to new challenges. Strong interpersonal skills with the ability to collaborate effectively and respectfully in diverse teams. Able to present ideas clearly, actively listen, and contribute to group decision-making. Additional Responsibilities: Participate in the design or redesign of tools and equipment to improve manufacturing processes. Ensure employee safety and compliance with health and safety regulations. Monitor, test and maintain production equipment to ensure operational efficiency. Collect and analyze production data for continuous improvement. Support cost control initiatives and contribute to maintaining operations within budget.

Octubre 16 2026 en Mexicali