Senior Quality Engineer, MedTech — QA & V&V Leader

Johnson & Johnson MedTech; Ciudad Juárez; Presencial; MXN 600.000 - 900.000; Jornada completa

Descripción de la vacante

Johnson & Johnson MedTech in Ciudad Juárez, Mexico, invites applications for a Senior Quality Engineer at the Salvarcar Plant. You will lead quality engineering activities, drive design verification, process validations, and CAPA implementation to ensure product conformance across lifecycle.

The role requires strong knowledge of GMP, ISO 13485, and regulatory standards, plus mentoring junior engineers and cross-functional collaboration with operations, regulatory affairs, and suppliers in a

Formación

• Bachelor's degree in a related field and 4–6 years of quality, manufacturing, or R&D experience in a medical device or regulated industry.
• Master's degree preferred; ASQ certification and Six Sigma experience are desirable.
• Knowledge of GMP, QSR, and quality engineering tools for product development and lifecycle management.

Responsabilidades

• Develop and implement quality standards and processes across product lifecycle.
• Lead design verification tests, process validations, and CAPA activities.
• Use statistical tools to analyze data and improve process capability.
• Support design reviews, validation protocols, and supplier quality as needed.
• Mentor junior engineers and collaborate with cross-functional teams to ensure compliance.

Conocimientos

Analytical Reasoning

Coaching

Customer Centricity

Data Savvy

Document Management

Financial Competence

GAMP

Lean Manufacturing

Process Improvements

Quality Standards

Quality Systems

Quality Validation

STEM

Supervision

Supply Planning

Technologically Savvy

Educación

Bachelor's degree in a related field

Master's degree

Descripción del empleo

Johnson & Johnson MedTech in Ciudad Juárez, Mexico, invites applications for a Senior Quality Engineer at the Salvarcar Plant. You will lead quality engineering activities, drive design verification, process validations, and CAPA implementation to ensure product conformance across lifecycle.

The role requires strong knowledge of GMP, ISO 13485, and regulatory standards, plus mentoring junior engineers and cross-functional collaboration with operations, regulatory affairs, and suppliers in a