- Fondo de ahorro
- Transporte
- Servicios medicos en planta
- bonos anuales
- Beneficios de acuerdo a la LFT

Quality Engineer
Thermo Fisher Scientific (Planta Tijuana)
Tijuana, Baja California
Enero 09 2026
Corporativo
Giro
Maquiladora (Export.)
Actividad principal
Manufactura, empaque de artículos médicos desechables y moldeo por inyección.
Número de empleados
1000
Sitio Web corporativo
Descripción y detalle de las actividades
Coordinates subordinates in the inspection and/or receiving testing and/or process and finished products, according to established procedures.
- Coordinates Tijuana plant activities related to the customer complaints.
- Coordinates customer-complaint related CAPA (Corrective Action and Preventive Action) at the Tijuana plant. Works with various departments to identify the root cause of problems, define the necessary actions required to assure corrective and preventative actions are properly implemented and documented.
- Perform the task of verification of the effectiveness of the CAPAs.
- Participate in the process and product improvement plans.
- Participates actively to cost reduction and PPI programs
- Give support to Quality Assurance & Quality Manager to attend observations of ISO 9001 and ISO 13485 certification process apply to his area
- Coordinates the initiation and closure of internal non conformances(NCMs)
- Participates/Leads CAPA investigation
- Participates/Leads internal audits
- Participates/Leads internal and external (customer) meetings as required.
- Supervises a group of Quality inspectors
- Conducts trend analysis
- Other duties may be assigned, as required.
Experiencia y requisitos
Bachelor degree in Engineering or Science or equivalent training and /or experience, with focus on Industrial Engineering and/or Quality Engineering.
- MS Office (Word, Excel, Access and PowerPoint) intermediate level.
- Statistical software knowledge (minitab)
- At least 3-5 years of experience in an ISO 9001 and/or ISO 13485 certified medical-device manufacturing company.
-Injection molding
- Knowledge of Lean manufacturing process.
- Hands-on experience in CAPA Process.
- Experience with Failure Mode and Effect analysis tools.
- Experience with problem-solving techniques such as Fishbone diagram, Process Review, C&E, 5 Whys among others.
- Knowledge of ISO 9001 and ISO 13485 standards.
- Advanced English Level (Reading, conversation, able to do fluid presentations).
- Certificated in ASQ, Six Sigma, ISO 13485 Internal/Lead auditor. (Desirable)
***Validaciones, Bases estadísticas, experiencia en moldeo por inyección,****
Beneficios
Número de vacantes 1
Área Calidad
Contrato Permanente
Modalidad Presencial
Turno Diurno
Jornada Tiempo Completo
- Tiempo completo
Estudios Carrera con título profesional
Inglés Hablado: Avanzado, Escrito: Intermedio
Disponibilidad p. viajar No
