Senior Quality Lifecycle Engineer – MedTech Innovation

Johnson And Johnson; Ciudad Juárez; Presencial; MXN 420.000 - 630.000; Jornada completa

Descripción de la vacante

Johnson & Johnson in Ciudad Juárez, Mexico seeks a Senior Quality Life Cycle Engineer to lead quality engineering across the product life cycle, emphasizing reliability, risk management, statistics, and design control from development to manufacturing.

You will ensure compliance with GMP, ISO 13485, ISO 14971, and related standards, lead audits, review technical documentation, and drive corrective actions and continuous improvement with cross-functional teams.

Formación

• Bachelor's degree in engineering from an accredited school is required; Mechanical, Electrical, or Biomedical preferred.
• Advanced degrees are a plus; STEM graduates with technical training considered.
• Experience in a regulated medical technology/biotech environment is preferred.

Responsabilidades

• Lead quality engineering to support product life cycle and reliability.
• Apply risk management, statistics, and design control across projects.
• Audit readiness and collaboration with development, manufacturing, and suppliers.
• Review engineering docs and approve changes ensuring quality requirements.
• Address root causes and drive corrective/preventive actions.

Conocimientos

Analytical reasoning

Computerized equipment skills

Emerging technologies

Gemba kaizen

Issue escalation

Lean supply chain management

Problem solving

Process control

Process engineering

Process oriented

Product improvements

STEM applications

Situational awareness

Technical research

Validation testing

Educación

Bachelor's degree in engineering (Mechanical / Electrical / Biomedical)

Descripción del empleo

Johnson & Johnson in Ciudad Juárez, Mexico seeks a Senior Quality Life Cycle Engineer to lead quality engineering across the product life cycle, emphasizing reliability, risk management, statistics, and design control from development to manufacturing.

You will ensure compliance with GMP, ISO 13485, ISO 14971, and related standards, lead audits, review technical documentation, and drive corrective actions and continuous improvement with cross-functional teams.