Senior Internal Auditor, Regulated Quality & Compliance

Agilent Technologies; España; Presencial; EUR 70.000 - 100.000; Jornada completa

Descripción de la vacante

Agilent Technologies is seeking a Lead Internal Auditor within the Customer Quality & Compliance team. You will plan, lead, and execute risk-based internal audits across regulated medical devices and pharmaceutical environments, ensuring QMS compliance with ISO 9001/13485, FDA cGMP/QSR, EU GMP, IVDR, and ICH.

You will also support inspection readiness, train sites, and report findings. Travel up to 50% globally, with potential remote or EU/UK site options; requires 8+ years in regulated QA/audit

Formación

• Bachelor’s degree in science, engineering, or related field.
• 8+ years’ experience in regulated quality systems, internal auditing, or regulatory compliance within pharmaceutical/medical device industries.
• 5+ years’ experience as a Lead Internal Auditor, ISO 13485 Lead Auditor certification required.

Responsabilidades

• Lead and conduct risk-based internal audits across pharmaceutical and medical device operations.
• Serve as Lead Auditor for complex, cross-functional, multi-site audits.
• Assess QMS compliance and effectiveness against ISO 9001, ISO 13485, FDA cGMP/QSR, EU GMP, IVDR, and ICH requirements.

Conocimientos

Analytical thinking

Risk-based auditing

Communication skills

Educación

Bachelor's degree in science/engineering

Advanced degree preferred

Descripción del empleo

Agilent Technologies is seeking a Lead Internal Auditor within the Customer Quality & Compliance team. You will plan, lead, and execute risk-based internal audits across regulated medical devices and pharmaceutical environments, ensuring QMS compliance with ISO 9001/13485, FDA cGMP/QSR, EU GMP, IVDR, and ICH.

You will also support inspection readiness, train sites, and report findings. Travel up to 50% globally, with potential remote or EU/UK site options; requires 8+ years in regulated QA/audit