Senior Process Engineer, MedTech Supply Chain

8286-Cordis De Mexico Legal Entity; Ciudad Juárez; Presencial; MXN 600.000 - 900.000; Jornada completa

Descripción de la vacante

Johnson &Johnson in Juarez is seeking a Sr Process Engineer to develop and manage complex Process Engineering projects within the supply chain, directing milestones and ensuring GMP-compliant documentation.

The role requires 4–6 years in a similar field, medical industry experience, and strong analytical skills including DOE and statistics, with advanced English and Spanish written ability for cross-functional communication.

Formación

• Engineering field and Master of Science or certification recommended.
• 4–6 years in a similar Process Engineering role.
• Experience in medical industry preferred.
• Knowledge of GMP and medical documentation preferred.
• Design of experiments and statistical methods required.
• Spanish written and English advanced communication.

Responsabilidades

• Develop complex Process Engineering supply chain project plans, milestones and objectives.
• Oversee communication of non-conformances and implement corrective actions.
• Configure performance reports and provide status updates to management.
• Administer process validations for integration and supply chain implementation.
• Lead Process Engineering Technician activities and ensure safety compliance.
• Escalate and monitor process engineering issues to the next management level.
• Coach junior colleagues in techniques and responsibilities.
• Apply Johnson & Johnsons Credo and Leadership Imperatives daily.

Conocimientos

Process Engineering

Design of experiments

Statistical analysis

GMP documentation

Advanced English

Spanish (written)

Statistical software

Computational packages

Educación

Master of Science or Certification recommended

Herramientas

Statistical software

Computational packages

Descripción del empleo

Johnson &Johnson in Juarez is seeking a Sr Process Engineer to develop and manage complex Process Engineering projects within the supply chain, directing milestones and ensuring GMP-compliant documentation.

The role requires 4–6 years in a similar field, medical industry experience, and strong analytical skills including DOE and statistics, with advanced English and Spanish written ability for cross-functional communication.