Hybrid Manufacturing Quality Investigator: Deviations & CAPA

Novartis; Ciudad de México; Híbrido; MXN 480.000 - 640.000; Jornada completa

Descripción de la vacante

Novartis in Mexico City is seeking a quality-focused Manufacturing Deviation Investigator to drive investigations and CAPAs within GMP. You will lead end-to-end deviation work, assess product impact, and translate findings into effective corrective actions, ensuring robust prevention of recurrence.

The role requires leadership in root-cause analysis, collaboration across functions, and weekend rotation with five-day weeks. Fluency in English and Spanish is essential.

Formación

• Bachelor's degree in a scientific field with 2–5 years in pharma.
• Proven GMP production experience, aseptic/sterile preferred.
• Experience leading deviation investigations and CAPAs.
• Fluent in English and Spanish, written and spoken.

Responsabilidades

• Open and assess deviations, determining criticality within timelines.
• Evaluate product impact in line with batch release activities.
• Author and own investigations with clear scope and root cause.
• Apply root cause analysis to identify deviations in product and process.
• Develop and implement CAPAs; verify effectiveness.
• Support manufacturing operations during deviations and train staff.

Conocimientos

Deviation investigations

GMP experience

Root cause analysis

Bilingual English/Spanish

Shift work

Educación

Bachelor's degree in science

Descripción del empleo

Novartis in Mexico City is seeking a quality-focused Manufacturing Deviation Investigator to drive investigations and CAPAs within GMP. You will lead end-to-end deviation work, assess product impact, and translate findings into effective corrective actions, ensuring robust prevention of recurrence.

The role requires leadership in root-cause analysis, collaboration across functions, and weekend rotation with five-day weeks. Fluency in English and Spanish is essential.