- Beneficios de acuerdo a la LFT
- servicios médicos en planta
Correo de contacto
*****@tecma.com
Giro
Maquiladora (Export.)
Actividad principal
Prestadora de servicios administrativos principalmente a industrias maquiladoras.
Número de empleados
5000
Sitio Web
Descripción y detalle de las actividades
Process Ownership & Stability
· Own end-to-end manufacturing processes (SMT, THT, Box Build, Final Assembly, Test).
· Define, control, and optimize process parameters to ensure consistent output.
· Lead process validation activities (IQ/OQ/PQ) in regulated and non-regulated environments.
· Ensure proper change control for process changes.
Continuous Improvement
· Drive yield improvement, scrap reduction, and rework elimination.
· Lead root cause analysis (8D, A3, Fishbone, 5 Whys) and corrective actions.
· Implement Lean Manufacturing and Six Sigma methodologies.
· Improve line balance, throughput, capacity, and OEE.
Team Leadership
· Lead, coach, and develop Process Engineers and Industrial Engineers.
· Define workload priorities aligned with production needs.
· Ensure technical depth and discipline within the PE team.
· Promote a culture of accountability, data-driven decision-making, and ownership.
Cross-Functional Collaboration
· Partner with Manufacturing Engineering during NPI and ramp-up to ensure smooth handoff to production.
· Work closely with Operations to support daily production and issue resolution.
· Support Quality in audits, customer visits, and regulatory inspections (ISO 13485, FDA, IPC).
· Collaborate with Program Management on capacity, risk, and execution planning.
Metrics & Reporting
· Define and track KPIs such as yield, scrap, rework, cycle time, OEE, and process capability.
· Use data and SPC to drive decisions and improvements.
· Provide regular reporting to Operations and leadership.
Experiencia y requisitos
Experience in:
Key Performance Indicators (KPIs)
· First Pass Yield (FPY)
· Scrap and Rework Rate
· OEE / Throughput
· Process Capability (Cp/Cpk)
· Audit Findings related to process control
Education
· Bachelor’s degree in Engineering (Industrial, Manufacturing, Mechanical, Electrical, or related).
Experience
· 7+ years of experience in process engineering within an EMS or high-mix manufacturing environment.
· 3+ years in a leadership or people management role.
· Strong hands-on experience with SMT and electronics assembly processes.
· Experience supporting regulated industries (medical devices preferred).
Technical Skills
· Process validation (IQ/OQ/PQ)
· SPC and statistical analysis
· Lean / Six Sigma tools
· SMT process optimization and defect analysis
· Familiarity with IPC standards (IPC-A-610, J-STD-001)
· Understanding of ISO 9001 / ISO 13485 and FDA QS
🧠 Soft Skills & Competencies
· Strong leadership and coaching skills
· Structured problem-solving mindset
· Ability to manage priorities in a fast-paced environment
· Excellent communication across technical and non-technical teams
· Data-driven and detail-oriented
· Experience in medical device manufacturing within an EMS environment
· Exposure to customer and regulatory audits
· Experience scaling operations or supporting rapid growth
Beneficios
Número de vacantes 1
Área Ingeniería
Contrato Permanente
Modalidad Presencial
Turno Diurno
Jornada Tiempo Completo
- Tiempo completo
- Turno Matutino
Estudios Carrera con título profesional
Inglés Hablado: Avanzado, Escrito: Avanzado
Disponibilidad p. viajar No

