Manufacturing Engineer: Process Validation & CI, Querétaro

Abbott; Santiago de Querétaro; Presencial; MXN 300.000 - 520.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Career development

Global employer recognition

Diversity commitment

Descripción de la vacante

Abbott in Querétaro, Mexico, seeks a Manufacturing Engineer to develop and implement efficient manufacturing processes aligned with quality standards. You will install and validate assembly lines, manage process documentation, and oversee equipment acquisition to support high-quality product manufacture.

The role requires a Bachelor's degree and 5 years of experience, with fluency in English and Spanish. ISO9001, GMP, and FDA experience is preferred, with ongoing Lean initiatives and continuous

Formación

• Bachelor's degree required in a relevant field.
• 5 years of professional experience in manufacturing engineering or a related role.
• Ability to clearly articulate manufacturing concepts in English and Spanish.
• Experience with ISO9001, GMPs, and FDA regulations.

Responsabilidades

• Installation and validation of manufacturing processes.
• Development and administration of manufacturing process documentation.
• Acquisition, purchase and administration of manufacturing equipment and tools.
• Investigation and resolution of manufacturing process and equipment problems.
• Continuous improvement projects to reduce costs and increase efficiency in manufacturing lines.
• Training direct labor on basic equipment problem solving.

Conocimientos

Manufacturing processes

Process validation

Problem solving

Lean Manufacturing

English and Spanish communication

Educación

Bachelor's degree

Descripción del empleo

Abbott in Querétaro, Mexico, seeks a Manufacturing Engineer to develop and implement efficient manufacturing processes aligned with quality standards. You will install and validate assembly lines, manage process documentation, and oversee equipment acquisition to support high-quality product manufacture.

The role requires a Bachelor's degree and 5 years of experience, with fluency in English and Spanish. ISO9001, GMP, and FDA experience is preferred, with ongoing Lean initiatives and continuous