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Manufacturing Engineer (AR)

Grupo TECMA

Tijuana

Presencial

MXN 549,000 - 916,000

Jornada completa

Hoy
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Descripción de la vacante

A manufacturing company in Tijuana is seeking a results-driven Manufacturing Engineer with a background in the electronics industry. The ideal candidate has 3 to 5 years of experience, strong analytical skills, and proficiency in English. Responsibilities include providing technical support, leading process validations, and collaborating with cross-functional teams to enhance manufacturing processes.

Formación

  • 3–5 years of experience in a manufacturing environment, preferably in electronics, SMT, or medical devices.
  • Strong knowledge of manufacturing processes and continuous improvement methodologies.
  • Familiarity with ISO 13485, IPC standards, or FDA regulations is a plus.

Responsabilidades

  • Provide technical support to ensure high quality and efficiency.
  • Lead or support process validation activities according to applicable standards.
  • Identify and implement improvements to reduce waste and increase throughput.

Conocimientos

Fluent in English
Analytical and problem-solving
Technically skilled
Lean principles knowledge

Educación

Bachelor's degree in Industrial, Mechanical, Electronics, or Manufacturing Engineering

Herramientas

Microsoft Office
CAD or SolidWorks
Descripción del empleo

We are looking for a results-driven Manufacturing Engineer with 3 to 5 years of experience in the electronics industry, preferably with a background in SMT (Surface Mount Technology) or medical device manufacturing. The ideal candidate is fluent in English, technically skilled, and capable of driving continuous improvement and supporting NPI (New Product Introduction) efforts.

Key Responsibilities
  • Provide technical support to the production floor for daily operations, ensuring high quality and efficiency.
  • Develop and maintain process documentation, including work instructions, process flows, and control plans.
  • Lead or support process validation activities (IQ/OQ/PQ) in accordance with ISO 13485 or other applicable standards.
  • Identify and implement improvements in manufacturing processes to reduce waste, improve yield, and increase throughput.
  • Collaborate with cross-functional teams (Quality, Supply Chain, Engineering, and Program Management) to support product launches and changes.
  • Troubleshoot process issues using root cause analysis and implement corrective and preventive actions.
  • Participate in the selection and qualification of new equipment and tooling.
  • Ensure compliance with safety, quality, and regulatory requirements.
  • Lead and participate in meetings with customers and suppliers, providing updates and technical discussions in English.
Qualifications
  • Bachelor’s degree in Industrial, Mechanical, Electronics, or Manufacturing Engineering.
  • 3–5 years of experience in a manufacturing environment, preferably in electronics, SMT, or medical devices.
  • Strong knowledge of manufacturing processes, lean principles, and continuous improvement methodologies.
  • Familiarity with ISO 13485, IPC standards, or FDA regulations is a plus.
  • Excellent verbal and written communication skills in English. Able to confidently lead meetings with customers and suppliers.
  • Proficient in Microsoft Office and CAD or SolidWorks; experience with MES or ERP systems is a plus.
  • Strong analytical and problem-solving skills.
  • Ability to work independently and as part of a team in a fast-paced environment.
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